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Details

Stereochemistry ACHIRAL
Molecular Formula C3H9BO3
Molecular Weight 103.913
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Trimethyl borate

SMILES

COB(OC)OC

InChI

InChIKey=WRECIMRULFAWHA-UHFFFAOYSA-N
InChI=1S/C3H9BO3/c1-5-4(6-2)7-3/h1-3H3

HIDE SMILES / InChI
Molecular Formula C3H9BO3
Molecular Weight 103.913
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
149124
PubMed

PubMed

TitleDatePubMed
Identification and counting of carbonyl and hydroxyl functionalities in protonated bifunctional analytes by using solution derivatization prior to mass spectrometric analysis via ion-molecule reactions.
2010-05
New preparation and synthetic reactions of 3,3,3-trifluoropropynyllithium, -borate and -stannane: facile synthesis of trifluoromethylated allenes, arylacetylenes and enynes.
2009-08
tert-Butyl 2-borono-1H-pyrrole-1-carboxyl-ate.
2009-03-06
2-[Bis(2-amino-ethyl)amino]ethanaminium chloride dichloro-methane solvate.
2008-11-29
Identification of the carboxylic acid functionality by using electrospray ionization and ion-molecule reactions in a modified linear quadrupole ion trap mass spectrometer.
2008-05-01
Coupling of ion-molecule reactions with liquid chromatography on a quadrupole ion trap mass spectrometer.
2008-04
(2-Meth-oxy-1,3-phenyl-ene)diboronic acid.
2008-01-09
Facile and efficient synthesis of C-hydroxycarboranes and C,C'-dihydroxycarboranes.
2007-05-14
Noncryogenic I/Br-Mg exchange of aromatic halides bearing sensitive functional groups using i-PrMgCl-bis[2-(N,N-dimethylamino)ethyl] ether complexes.
2006-01-19
Manipulating the fragmentation patterns of phosphopeptides via gas-phase boron derivatization: determining phosphorylation sites in peptides with multiple serines.
2005-12
Contrasteric stereochemical dictation of the cyclobutene ring-opening reaction by a vacant boron p orbital.
2005-02-09
Influences of electronic effects and anions on the enantioselectivity in the oxazaborolidine-catalyzed asymmetric borane reduction of ketones.
2004-10-01
Simple synthesis of diastereomerically pure phosphatidylglycerols by phospholipase D-catalyzed transphosphatidylation.
2004-10
Gas-phase synthesis and reactivity of the organomagnesates [CH3MgL2]- (L = Cl and O2CCH3): from ligand effects to catalysis.
2004-09-29
Kinetic measurements of phosphoglucomutase by direct analysis of glucose-1-phosphate and glucose-6-phosphate using ion/molecule reactions and Fourier transform ion cyclotron resonance mass spectrometry.
2004-06-15
Surface acoustic waves for the characterization of BN-coated fibres observed by Brillouin light scattering.
2004-06
Chloromethyl chlorosulfate: a new, catalytic method of preparation and reactions with some nucleophiles.
2004-05-21
Effect of temperature on the enantioselectivity in the oxazaborolidine-catalyzed asymmetric reduction of ketones. Noncatalytic borane reduction, a nonneglectable factor in the reduction system.
2003-12-26
Investigation of ion/molecule reactions as a quantification method for phosphorylated positional isomers. an FT-ICR approach.
2003-08
Versatile synthesis of 3,5-disubstituted 2-fluoropyridines and 2-pyridones.
2003-04-18
Short synthesis of 2-methoxyestradiol and 2-hydroxyestradiol.
2003-04
Probing isomeric differences of phosphorylated carbohydrates through the use of ion/molecule reactions and FT-ICR MS.
2003-04
Large-scale synthesis and structure of boron nitride sub-micron spherical particles.
2002-12-07
Structure and composition studies of chemical vapour-deposited BCN fibre coatings.
2002-10
Gas phase reactions of trimethyl borate with phosphates and their non-covalent complexes.
2002-09
Analysis of phosphate position in hexose monosaccharides using ion-molecule reactions and SORI-CID on an FT-ICR mass spectrometer.
2002-06-01
Efficient and convenient nonaqueous workup procedure for the preparation of arylboronic esters.
2002-02-08
Patents

Patents

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06495568
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Substance Class Chemical
Created
by admin
on Mon Mar 31 19:59:17 GMT 2025
Edited
by admin
on Mon Mar 31 19:59:17 GMT 2025
Record UNII
82U64J6F5N
Record Status Validated (UNII)
Record Version
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Name Type Language
Trimethyl borate
HSDB   MI  
Systematic Name English
NSC-777
Preferred Name English
TRIMETHYL BORATE [MI]
Common Name English
BORIC ACID TRIMETHYL ESTER
Systematic Name English
TRIMETHYL BORATE [HSDB]
Common Name English
METHYL BORATE
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID0037738
Created by admin on Mon Mar 31 19:59:17 GMT 2025 , Edited by admin on Mon Mar 31 19:59:17 GMT 2025
PRIMARY
SMS_ID
300000053668
Created by admin on Mon Mar 31 19:59:17 GMT 2025 , Edited by admin on Mon Mar 31 19:59:17 GMT 2025
PRIMARY
NSC
777
Created by admin on Mon Mar 31 19:59:17 GMT 2025 , Edited by admin on Mon Mar 31 19:59:17 GMT 2025
PRIMARY
PUBCHEM
8470
Created by admin on Mon Mar 31 19:59:17 GMT 2025 , Edited by admin on Mon Mar 31 19:59:17 GMT 2025
PRIMARY
MERCK INDEX
m11152
Created by admin on Mon Mar 31 19:59:17 GMT 2025 , Edited by admin on Mon Mar 31 19:59:17 GMT 2025
PRIMARY Merck Index
MESH
C102081
Created by admin on Mon Mar 31 19:59:17 GMT 2025 , Edited by admin on Mon Mar 31 19:59:17 GMT 2025
PRIMARY
FDA UNII
82U64J6F5N
Created by admin on Mon Mar 31 19:59:17 GMT 2025 , Edited by admin on Mon Mar 31 19:59:17 GMT 2025
PRIMARY
CHEBI
38913
Created by admin on Mon Mar 31 19:59:17 GMT 2025 , Edited by admin on Mon Mar 31 19:59:17 GMT 2025
PRIMARY
HSDB
5589
Created by admin on Mon Mar 31 19:59:17 GMT 2025 , Edited by admin on Mon Mar 31 19:59:17 GMT 2025
PRIMARY
WIKIPEDIA
TRIMETHYL BORATE
Created by admin on Mon Mar 31 19:59:17 GMT 2025 , Edited by admin on Mon Mar 31 19:59:17 GMT 2025
PRIMARY
CAS
121-43-7
Created by admin on Mon Mar 31 19:59:17 GMT 2025 , Edited by admin on Mon Mar 31 19:59:17 GMT 2025
PRIMARY
ECHA (EC/EINECS)
204-468-9
Created by admin on Mon Mar 31 19:59:17 GMT 2025 , Edited by admin on Mon Mar 31 19:59:17 GMT 2025
PRIMARY
NIH
NCATS
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