Derivados del ácido borínico

Ácido fenilborónico, + 98 %, puede contener cantidades variables de anhídrido, Thermo Scientific Chemicals

CAS: 98-80-6 Fórmula molecular: C6H7BO2 Peso molecular (g/mol): 121.93 Número MDL: MFCD00002103 Clave InChI: HXITXNWTGFUOAU-UHFFFAOYSA-N Sinónimo: benzeneboronic acid,boronic acid, phenyl,phenyl boronic acid,phenylboric acid,dihydroxyphenylborane,phenyldihydroxyborane,dihydroxy phenyl borane,phenylboronicacid,borophenylic acid,usaf bo-2 PubChem CID: 66827 ChEBI: CHEBI:44923 Nombre IUPAC: ácido fenilborónico SMILES: OB(O)C1=CC=CC=C1

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1-Metil-4-(4,4,5,5-tetrametil-1,3,2-dioxaborolan-2-il)-1H-pirazol, 97+ %, Thermo Scientific Chemicals

CAS: 761446-44-0 Fórmula molecular: C10H17BN2O2 Peso molecular (g/mol): 208.07 Número MDL: MFCD03789259 Clave InChI: UCNGGGYMLHAMJG-UHFFFAOYSA-N Sinónimo: 1-methyl-4-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl-1h-pyrazole,1-methylpyrazole-4-boronic acid pinacol ester,1-methyl-4-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl pyrazole,1-methyl-1h-pyrazole-4-boronic acid pinacol ester,1-methyl-4-tetramethyl-1,3,2-dioxaborolan-2-yl-1h-pyrazole,1-methyl-pyrazole-4-boronic acid pinacol ester,1-methyl-4-4,4,5,5-tetramethyl-1,3,2 dioxaborolan-2-yl-1h-pyrazole,1h-pyrazole, 1-methyl-4-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl,1-methyl-4-tetramethyl-1,3,2-dioxaborolan-2-yl pyrazole,1-methyl-4-pyrazoleboronic acid pinacol ester PubChem CID: 2773987 SMILES: CN1C=C(C=N1)B1OC(C)(C)C(C)(C)O1

Ácido benceneborónico, +98 %, Thermo Scientific Chemicals

CAS: 98-80-6 Fórmula molecular: C6H7BO2 Peso molecular (g/mol): 121.93 Número MDL: MFCD00002103 Clave InChI: HXITXNWTGFUOAU-UHFFFAOYSA-N Sinónimo: benzeneboronic acid,boronic acid, phenyl,phenyl boronic acid,phenylboric acid,dihydroxyphenylborane,phenyldihydroxyborane,dihydroxy phenyl borane,phenylboronicacid,borophenylic acid,usaf bo-2 PubChem CID: 66827 ChEBI: CHEBI:44923 Nombre IUPAC: ácido fenilborónico SMILES: OB(O)C1=CC=CC=C1

Ácido 4-cianobencenoborónico, 98 %, Thermo Scientific Chemicals

CAS: 126747-14-6 Fórmula molecular: C7H6BNO2 Peso molecular (g/mol): 146.94 Número MDL: MFCD01318968 Clave InChI: CEBAHYWORUOILU-UHFFFAOYSA-N Sinónimo: 4-cyanophenyl boronic acid,4-cyanobenzeneboronic acid,4-dihydroxyboranyl benzonitrile,4-cyano-phenyl-boronic acid,4-boronobenzonitrile,p-cyanophenylboronic acid,4-cyanobenzene boronic acid,boronic acid, 4-cyanophenyl,4-cyano-phenyl boronic acid PubChem CID: 2734326 Nombre IUPAC: ácido (4-cianofenil)borónico SMILES: OB(O)C1=CC=C(C=C1)C#N

Ácido (2-metilpropil)borónico, 95+%

CAS: 84110-40-7 Fórmula molecular: C4H11BO2 Peso molecular (g/mol): 101.94 Número MDL: MFCD00134156 Clave InChI: ZAZPDOYUCVFPOI-UHFFFAOYSA-N Sinónimo: isobutylboronic acid,isobutaneboronic acid,2-methylpropyl boronic acid,1-isobutaneboronic acid,2-methylpropaneboronic acid,2-methylprop-1-ylboronic acid,unii-khx76h7jhz,khx76h7jhz,2-methyl-1-propylboronic acid,2-methyl-1-propaneboronic acid PubChem CID: 2734395 Nombre IUPAC: ácido 2-metilpropilborónico SMILES: CC(C)CB(O)O

Ácido 1-naftalenoborónico, 97 %, Thermo Scientific Chemicals

CAS: 13922-41-3 Fórmula molecular: C10H9BO2 Peso molecular (g/mol): 171.99 Número MDL: MFCD00019722 Clave InChI: HUMMCEUVDBVXTQ-UHFFFAOYSA-N Sinónimo: 1-naphthaleneboronic acid,1-naphthylboronic acid,naphthalene-1-boronic acid,naphthalenyl-1-boronic acid,1-naphthalene boronic acid,1-naphthaleneboronicacid,1-naphthyleneboronic acid,boronic acid, naphthalenyl,1-borononaphthalene,naphthylboronic acid PubChem CID: 254532 Nombre IUPAC: ácido naftalen-1-ilborónico SMILES: OB(O)C1=CC=CC2=CC=CC=C12

Ácido piridina-4-borónico, 97 %, Thermo Scientific™

CAS: 1692-15-5 Fórmula molecular: C5H6BNO2 Peso molecular (g/mol): 122.92 Número MDL: MFCD01074545 Clave InChI: QLULGIRFKAWHOJ-UHFFFAOYSA-N Sinónimo: pyridine-4-boronic acid,4-pyridineboronic acid,4-pyridylboronic acid,pyridin-4-yl boronic acid,4-pyridinylboronic acid,pyridin-4-yl-4-boronic acid,4-pyridinebornic acid,pyridyl-4-boronic acid,4-pyridinyl boronic acid,pyridine-4-ylboronic acid PubChem CID: 2734379 SMILES: OB(O)C1=CC=NC=C1

Ácido ciclopentilborónico, 95 %, Thermo Scientific Chemicals

CAS: 63076-51-7 Fórmula molecular: C5H11BO2 Peso molecular (g/mol): 113.951 Número MDL: MFCD01074541 Clave InChI: VTTDFSNKIMAQTB-UHFFFAOYSA-N Sinónimo: cyclopentaneboronic acid,boronic acid, cyclopentyl,cylopentyl boronic acid,cyclopentylboronicacid,pubchem7792,acmc-209ncu,--paclitaxel;paclitaxel,boronic acid, b-cyclopentyl,cyclopentylboronic acid PubChem CID: 2734327 Nombre IUPAC: ácido ciclopentilborónico SMILES: B(C1CCCC1)(O)O

Éster de pinacol de ácido 3-bromopropilborónico, 98 %, Thermo Scientific Chemicals

CAS: 124215-44-7 Fórmula molecular: C9H18BBrO2 Peso molecular (g/mol): 248.96 Número MDL: MFCD10567053 Clave InChI: CHQXFJUKMDJWHO-UHFFFAOYSA-N Sinónimo: 2-3-bromopropyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane,3-bromopropylboronic acid pinacol ester,1,3,2-dioxaborolane,2-3-bromopropyl-4,4,5,5-tetramethyl,acmc-1c5j4,3-bromopropylboronic acid, pinacol ester,2-3-bromopropyl-4?4?5?5-tetramethyl-1?3?2-dioxaborolane PubChem CID: 14836669 Nombre IUPAC: 2-(3-bromopropil)-4,4,5,5-tetrametil-1,3,2-dioxaborolano SMILES: CC1(C)OB(CCCBr)OC1(C)C

Ácido 2-ciano-3-metoxibencenoborónico, 95 %, Thermo Scientific Chemicals

Ácido 3-cloro-4-cianobencenoborónico, 96 %, Thermo Scientific Chemicals

CAS: 1008415-02-8 Fórmula molecular: C7H5BClNO2 Peso molecular (g/mol): 181.382 Clave InChI: QCJTUOIMDNJEHR-UHFFFAOYSA-N Sinónimo: 3-chloro-4-cyanophenyl boronic acid,boronic acid, b-3-chloro-4-cyanophenyl,acmc-2097sr,3-chloro-4-cyanophenyl boronicacid PubChem CID: 46738932 Nombre IUPAC: ácido (3-cloro-4-cianofenil)borónico SMILES: B(C1=CC(=C(C=C1)C#N)Cl)(O)O

Éster de pinacol de ácido isopropilborónico, 98 %, Thermo Scientific Chemicals

CAS: 76347-13-2 Fórmula molecular: C9H19BO2 Peso molecular (g/mol): 170.059 Número MDL: MFCD05663856 Clave InChI: MECCSFDHAVAAAW-UHFFFAOYSA-N Sinónimo: 2-isopropyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane,2-isopropylboronic acid, pinacol ester,2-isopropylboronic acid pinacol ester,isopropylboronic acid pinacol ester,4,4,5,5-tetramethyl-2-propan-2-yl-1,3,2-dioxaborolane,1,3,2-dioxaborolane, 4,4,5,5-tetramethyl-2-1-methylethyl,2-isopropyl-4,4,5,5-tetramethyl-1,3,2-dioxaborole,2-isoproyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane,2-methylethyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane PubChem CID: 12727711 Nombre IUPAC: 4,4,5,5-tetrametil-2-propan-2-il-1,3,2-dioxaborolano SMILES: B1(OC(C(O1)(C)C)(C)C)C(C)C

Ácido etilborónico, 98 %, Thermo Scientific Chemicals

CAS: 4433-63-0 Fórmula molecular: C2H7BO2 Peso molecular (g/mol): 73.89 Número MDL: MFCD01074536 Clave InChI: PAVZHTXVORCEHP-UHFFFAOYSA-N Sinónimo: boronic acid, ethyl,ethaneboronic acid,ethyldihydroxyborane,ethyl boronic acid,boronic acid, ethyl-9ci,ethylboronicacid,pubchem7960,ethylboric acid,etb oh 2 PubChem CID: 521157 Nombre IUPAC: ácido etilborónico SMILES: CCB(O)O

Pinacol éster de ácido alilborónico, 98 %, Thermo Scientific Chemicals

CAS: 72824-04-5 Fórmula molecular: C9H17BO2 Peso molecular (g/mol): 168.04 Número MDL: MFCD00013347 Clave InChI: YMHIEPNFCBNQQU-UHFFFAOYSA-N Sinónimo: allylboronic acid pinacol ester,2-allyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane,allylboronic acid, pinacol cyclic ester,4,4,5,5-tetramethyl-2-prop-2-en-1-yl-1,3,2-dioxaborolane,allylboronic acid piracol ester,1,3,2-dioxaborolane, 4,4,5,5-tetramethyl-2-2-propenyl,2-prop-2-en-1-yl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane,allylboronicacidpinacolester,pinacol allylboronate,abape PubChem CID: 2763171 Nombre IUPAC: 4,4,5,5-tetrametil-2-prop-2-enil-1,3,2-dioxaborolano SMILES: CC1(C)OB(CC=C)OC1(C)C

Ácido 2,3-diclorobencenoborónico, 98 %, Thermo Scientific Chemicals

CAS: 151169-74-3 Fórmula molecular: C6H5BCl2O2 Peso molecular (g/mol): 190.81 Número MDL: MFCD01075703 Clave InChI: TYIKXPOMOYDGCS-UHFFFAOYSA-N Sinónimo: 2,3-dichlorophenyl boronic acid,2,3-dichlorobenzeneboronic acid,2,3-dichlorophenyl boranediol,boronic acid, 2,3-dichlorophenyl,contains varying amounts of anhydride,pubchem1810,dichlorophenylboronic acid,acmc-1c0ur,dichlorobenzene boronic acid PubChem CID: 2734661 Nombre IUPAC: ácido (2,3-diclorofenil)borónico SMILES: OB(O)C1=C(Cl)C(Cl)=CC=C1