Home Other Building Blocks 2,3,4-Trimethylbenzoic acid

2,3,4-Trimethylbenzoic acid

CAS No.:
1076-47-7
Catalog Number:
AG0094RK
Molecular Formula:
Molecular Weight:
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
250mg
95%
1 week
United States
$409
- +
Product Description
Catalog Number:
AG0094RK
Chemical Name:
2,3,4-Trimethylbenzoic acid
CAS Number:
1076-47-7
MDL Number:
MFCD20638198
IUPAC Name:
2,3,4-trimethylbenzoic acid
InChI:
InChI=1S/C10H12O2/c1-6-4-5-9(10(11)12)8(3)7(6)2/h4-5H,1-3H3,(H,11,12)
InChI Key:
HDIJZFORGDBEKL-UHFFFAOYSA-N
Properties
Complexity:
177  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
164.084g/mol
Formal Charge:
0
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
164.204g/mol
Monoisotopic Mass:
164.084g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
37.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.5  
Literature
Title Journal
Column selection and method development for the separation of nucleoside phosphotriester diastereoisomers, new potential anti-viral drugs. Application to cellular extract analysis. Biomedical chromatography : BMC 20050701
Enantiomeric resolution of new aromatase inhibitors by liquid chromatography on cellulose chiral stationary phases. Journal of separation science 20050301
Trimethylbenzoic acids as metabolite signatures in the biogeochemical evolution of an aquifer contaminated with jet fuel hydrocarbons. Journal of contaminant hydrology 20031201
Determination of the enantiomeric purity of nucleoside analogs related to d4T and acyclovir, new potential antiviral agents, using liquid chromatography on cellulose chiral stationary phases. Journal of chromatography. A 20021004
Diastereomeric resolution of nucleoside analogues, new potential antiviral agents, using high-performance liquid chromatography on polysaccharide-type chiral stationary phases. Journal of chromatography. A 20020111
Melatonin receptor agents: synthesis, resolution by HPLC on polysaccharides chiral stationary phases, absolute configuration, and pharmacology of the enantiomers of (+/-)-N-[[2[(7-fluoro-1,2,3,4-tetrahydronaphthalen-1-yl)ethyl]acetamide. Chirality 20010505
Direct separation of the stereoisomers of methoxytetrahydronaphthalene derivatives, new agonist and antagonist ligands for melatonin receptors, by liquid chromatography on cellulose chiral stationary phases. Journal of chromatography. A 20010112
Properties