Dioxaborolane

Bis-(pinakolato)-dibor, 98 %, Thermo Scientific Chemicals

CAS: 73183-34-3 Summenformel: C12H24B2O4 Molekulargewicht (g/mol): 253.94 MDL-Nummer: MFCD00799570 InChI-Schlüssel: IPWKHHSGDUIRAH-UHFFFAOYSA-N Synonym: bis pinacolato diboron,bis pinacolato diborane,4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi 1,3,2-dioxaborolane,pinacol diborane,diboron pinacol ester,b2pin2,4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi-1,3,2-dioxaborolane,4,4,5,5-tetramethyl-2-tetramethyl-1,3,2-dioxaborolan-2-yl-1,3,2-dioxaborolane,bispinacolate diboron,unii-i906w26p4u PubChem CID: 2733548 IUPAC-Name: 4,4,5,5-Tetramethyl-2-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-yl)-1,3,2-Dioxaborolan SMILES: CC1(C)OB(OC1(C)C)B1OC(C)(C)C(C)(C)O1

3-Aminobenzolboronsäurepinakolester, 97 %, Thermo Scientific Chemicals

CAS: 210907-84-9 Summenformel: C12H18BNO2 Molekulargewicht (g/mol): 219.09 MDL-Nummer: MFCD03453668 InChI-Schlüssel: YMXIIVIQLHYKOT-UHFFFAOYSA-N Synonym: 3-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl aniline,3-aminophenylboronic acid pinacol ester,benzenamine, 3-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl,3-aminophenylboronic acid, pinacol ester,3-tetramethyl-1,3,2-dioxaborolan-2-yl aniline,3-aminobenzeneboronic acid pinacol ester,3-aminophenylboronic acid, pinacol cyclic ester,3-aminophenylboronicacidpinacolester,apbe,amtb060 PubChem CID: 2734655 IUPAC-Name: 3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-yl)Anilin SMILES: CC1(C)OB(OC1(C)C)C1=CC=CC(N)=C1

3-[2-(Trimethylsilyl)-ethynyl]-benzolboronsäurepinakolester, 97 %, Thermo Scientific Chemicals

CAS: 915402-03-8 Summenformel: C17H25BO2Si Molekulargewicht (g/mol): 300.28 MDL-Nummer: MFCD08706285 InChI-Schlüssel: LDKJXCOLGXLWKP-UHFFFAOYSA-N Synonym: 4,4,5,5-tetramethyl-2-3-trimethylsilanylethynyl-phenyl-1,3,2 dioxaborolane,3-4,4,5,5-tetramethyl-1,3,2 dioxaborolan-2-yl-phenylethynyl-trimethylsilane,trimethyl 2-3-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl phenyl ethynyl silane,3-trimethylsilyl ethynyl phenylboronic acid pinacol ester,trimethyl 3-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl phenyl ethynyl silane,amtb201,3-2-trimethylsilyl ethynyl benzeneboronic acid pinacol ester PubChem CID: 17999151 SMILES: CC1(C)OB(OC1(C)C)C1=CC(=CC=C1)C#C[Si](C)(C)C

Bis-(pinakolato)-dibor, ≥ 98 %, Thermo Scientific Chemicals

CAS: 73183-34-3 Summenformel: C12H24B2O4 Molekulargewicht (g/mol): 253.94 MDL-Nummer: MFCD00799570 InChI-Schlüssel: IPWKHHSGDUIRAH-UHFFFAOYSA-N Synonym: bis pinacolato diboron,bis pinacolato diborane,4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi 1,3,2-dioxaborolane,pinacol diborane,diboron pinacol ester,b2pin2,4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi-1,3,2-dioxaborolane,4,4,5,5-tetramethyl-2-tetramethyl-1,3,2-dioxaborolan-2-yl-1,3,2-dioxaborolane,bispinacolate diboron,unii-i906w26p4u PubChem CID: 2733548 IUPAC-Name: 4,4,5,5-Tetramethyl-2-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-yl)-1,3,2-Dioxaborolan SMILES: CC1(C)OB(OC1(C)C)B1OC(C)(C)C(C)(C)O1

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Pinacolboran, 97 %, stabilisiert, Thermo Scientific Chemicals

CAS: 25015-63-8 Summenformel: C6H13BO2 Molekulargewicht (g/mol): 127.98 MDL-Nummer: MFCD00674030 InChI-Schlüssel: UCFSYHMCKWNKAH-UHFFFAOYSA-N Synonym: pinacolborane,4,4,5,5-tetramethyl-1,3,2-dioxaborolane,1,3,2-dioxaborolane, 4,4,5,5-tetramethyl,4,4,5,5-tetramethyl-1,3,2-dioxa-borolane,pinb-te,pubchem12688,acmc-209ggf,pinacolborane 5g,ksc489k6t,ucfsyhmckwnkah-uhfffaoysa-n PubChem CID: 6364989 IUPAC-Name: 4,4,5,5-Tetramethyl-1,3,2$l^{2}-Dioxaborolan SMILES: CC1(C)OBOC1(C)C

4,4,5,5-Tetramethyl-2-[2-(phenoxymethyl)-phenyl]-1,3,2-dioxaborolan, 97 %, Thermo Scientific™

CAS: 912569-55-2 Summenformel: C19H23BO3 Molekulargewicht (g/mol): 310.20 MDL-Nummer: MFCD09064986 InChI-Schlüssel: DTPMFYHICLWUGJ-UHFFFAOYSA-N Synonym: 4,4,5,5-tetramethyl-2-2-phenoxymethyl phenyl-1,3,2-dioxaborolane PubChem CID: 24229585 IUPAC-Name: 4,4,5,5-Tetramethyl-2-[2-(Phenoxymethyl)Phenyl]-1,3,2-Dioxaborolan SMILES: CC1(C)OB(OC1(C)C)C1=CC=CC=C1COC1=CC=CC=C1

3-Amino-2,4-difluorbenzolboronsäurepinakolester, 96 %, Thermo Scientific Chemicals

CAS: 1315692-91-1 Summenformel: C12H16BF2NO2 Molekulargewicht (g/mol): 255.072 MDL-Nummer: MFCD22419270 InChI-Schlüssel: MQGLBRAIKSVSIT-UHFFFAOYSA-N Synonym: 3-amino-2,4-difluorobenzeneboronic acid pinacol ester,2,6-difluoro-3-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl aniline,3-amino-2,4-difluorobenzeneboronicacidpinacolester,2,6-difluoro-3-4,4,5,5-tetramethyl-1,3,2-dioxaborolane-2-yl aniline PubChem CID: 99738339 IUPAC-Name: 2,6-Difluor-3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-yl)Anilin SMILES: B1(OC(C(O1)(C)C)(C)C)C2=C(C(=C(C=C2)F)N)F

2-Nitrobenzolboronsäurepinakolester, ≥ 98 %, Thermo Scientific Chemicals

CAS: 190788-59-1 Summenformel: C12H16BNO4 Molekulargewicht (g/mol): 249.07 MDL-Nummer: MFCD02179447 InChI-Schlüssel: VLJYUDGCEKORNG-UHFFFAOYSA-N Synonym: 4,4,5,5-tetramethyl-2-2-nitrophenyl-1,3,2-dioxaborolane,2-nitrobenzeneboronic acid pinacol ester,2-nitrophenyl boronic acid pinacol ester,2-nitrophenylboronic acid pinacol ester,1,3,2-dioxaborolane, 4,4,5,5-tetramethyl-2-2-nitrophenyl,2-2-nitrophenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane,2-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl nitrobenzene,amtb916,2-nitrophenyl boronic acid, pinacol ester,2-nitrophenylboronic acid, pinacol ester PubChem CID: 3699568 IUPAC-Name: 4,4,5,5-Tetramethyl-2-(2-Nitrophenyl)-1,3,2-Dioxaborolan SMILES: CC1(C)OB(OC1(C)C)C1=CC=CC=C1[N+]([O-])=O

4-[(Ethoxycarbonyl)-methyl]-phenylboronsäurepinakolester, 97 %, Thermo Scientific Chemicals

CAS: 859169-20-3 Summenformel: C16H23BO4 Molekulargewicht (g/mol): 290.17 MDL-Nummer: MFCD08704684 InChI-Schlüssel: RPRBNRDIESZHFL-UHFFFAOYSA-N Synonym: ethyl 2-4-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl phenyl acetate,4-ethoxycarbonylmethylphenyl boronic acid pinacol ester,4-ethoxycarbonylmethylphenyl boronic acid, pinacol ester,4-ethoxycarbonylmethyl phenylboronic acid, pinacol ester,4-ethoxycarbonylmethylphenylboronic acid pinacol ester,ethyl 2-4-tetramethyl-1,3,2-dioxaborolan-2-yl phenyl acetate,4-ethoxycarbonylmethylphenylboronic acid, pinacol ester,4-ethoxycarbonylmethyl phenylboronic acid pinacol ester,4-2-ethoxy-2-oxoethyl phenyl boronic acid pinacol ester PubChem CID: 46737998 IUPAC-Name: Ethyl 2-[4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-yl)Phenyl]Acetat SMILES: CCOC(=O)CC1=CC=C(C=C1)B1OC(C)(C)C(C)(C)O1

Pyrimidin-5-boronsäure, 97 %, Thermo Scientific™

2-Methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-phenol, 97 %, Thermo Scientific Chemicals

CAS: 269410-22-2 Summenformel: C13H19BO4 Molekulargewicht (g/mol): 250.10 MDL-Nummer: MFCD02093723 InChI-Schlüssel: WFSJROCEOJANPD-UHFFFAOYSA-N PubChem CID: 2734650 IUPAC-Name: 2-Methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-phenol SMILES: COC1=CC(=CC=C1O)B1OC(C)(C)C(C)(C)O1

4-[(tert-Butoxycarbonylamino)-methyl]-phenylboronsäurepinakolester, 97 %, Thermo Scientific Chemicals

CAS: 330794-35-9 Summenformel: C18H28BNO4 Molekulargewicht (g/mol): 333.24 MDL-Nummer: MFCD06409942 InChI-Schlüssel: CUDCEJRRWNIPDL-UHFFFAOYSA-N Synonym: 4-n-boc-aminomethyl phenylboronic acid pinacol ester,tert-butyl 4-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl benzylcarbamate,4-n-boc-amino methyl phenylboronic acid pinacol ester,4-tert-butoxycarbonylaminomethyl phenylboronic acid, pinacol ester,tert-butyl n-4-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl phenyl methyl carbamate,4-tert-butoxycarbonylaminomethyl phenylboronic acid pinacol ester,4-4,4,5,5-tetramethyl-1,3,2 dioxaborolan-2-yl-benzyl-carbamic acid tert-butyl ester,pubchem5247,4-n-boc-aminomethyl phenylboronic acid,pinacol ester PubChem CID: 3415442 IUPAC-Name: Tert-Butyl N-[[4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-yl)Phenyl]Methyl]Carbamat SMILES: CC(C)(C)OC(=O)NCC1=CC=C(C=C1)B1OC(C)(C)C(C)(C)O1

1-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-phenyl]-1H-pyrazol, 97 %, Thermo Scientific™

CAS: 852227-94-2 Summenformel: C15H19BN2O2 Molekulargewicht (g/mol): 270.14 MDL-Nummer: MFCD07368520 InChI-Schlüssel: GVSCNAOZDQCWJJ-UHFFFAOYSA-N Synonym: 1-3-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl phenyl-1h-pyrazole,1-3-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl phenyl pyrazole,1-3-tetramethyl-1,3,2-dioxaborolan-2-yl phenyl pyrazole,3-pyrazol-1-yl-phenylboronic acid pinacol ester,3-1h-pyrazol-1-yl benzeneboronic acid, pinacol ester,3-1h-pyrazol-1-yl phenyl boronic acid pinacol ester,4,4,5,5-tetramethyl-2-3-pyrazolylphenyl-1,3,2-dioxaborolane,1-3-4,4,5,5-tetramethyl-1,3,2 dioxaborolan-2-yl phenyl-1h-pyrazole,1-3-4,4,5,5-tetramethyl-1,3,2-dioxaboranlan-2-yl phenyl-1h-pyrazole PubChem CID: 4961249 IUPAC-Name: 1-[3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-yl)Phenyl]Pyrazol SMILES: CC1(C)OB(OC1(C)C)C1=CC(=CC=C1)N1C=CC=N1

2-[2-(2-Furyl)-phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolan, ≥ 97 %, Thermo Scientific™

CAS: 876316-28-8 Summenformel: C16H19BO3 Molekulargewicht (g/mol): 270.14 MDL-Nummer: MFCD08435879 InChI-Schlüssel: IKVHPKPYKOEGCK-UHFFFAOYSA-N Synonym: 2-2-fur-2-yl phenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane,2-2-furan-2-yl phenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane,2-2-2-furanyl phenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane,2-2-2-furyl phenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane PubChem CID: 18525792 IUPAC-Name: 2-[2-(Furan-2-yl)Phenyl]-4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan SMILES: CC1(C)OB(OC1(C)C)C1=CC=CC=C1C1=CC=CO1

4-Methoxy-trans-beta-styrylboronsäurepinakolester, 98 %, Thermo Scientific Chemicals

CAS: 149777-83-3 Summenformel: C15H21BO3 Molekulargewicht (g/mol): 260.14 MDL-Nummer: MFCD04038966 InChI-Schlüssel: VXSHTICWQKLRMP-UHFFFAOYSA-N Synonym: 4-methoxy-trans-beta-styrylboronic acid pinacol ester,e-2-4-methoxystyryl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane,2-2-4-methoxyphenyl ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane,1,3,2-dioxaborolane, 2-2-4-methoxyphenyl ethenyl-4,4,5,5-tetramethyl,2-e-2-4-methoxyphenyl ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane,4-methoxy-trans-beta-styrylboronicacidpinacolester,2-4-methoxyphenyl-vinylboronic acid pinacol ester,2-e-4-methoxystyryl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane,2-4-methoxystyryl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane,2-e-2-4-methoxyphenyl vinyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane PubChem CID: 15419573 IUPAC-Name: 2-[(E)2-(4-Methoxyphenyl)Ethenyl]-4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan SMILES: COC1=CC=C(C=CB2OC(C)(C)C(C)(C)O2)C=C1