2,3-Dimethylbenzoic acid

2,3-Dimethylbenzoic acid Basic information
Product Name:2,3-Dimethylbenzoic acid
Synonyms:2,3-Dimethylbenzoic acid,98%;2,3-dimethyl-benzoicaci;Hemellitic acid;hemelliticacid;2,3- twoMethyl benzoic acid;2,3-DIMETHYLBENZOIC ACID;RARECHEM AL BO 0357;O-XYLENE-3-CARBOXYLIC ACID
CAS:603-79-2
MF:C9H10O2
MW:150.17
EINECS:210-058-0
Product Categories:CARBOXYLICACID;intermediates;Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Carboxylic Acids;Phenyls & Phenyl-Het;Benzoic acid;Miscellaneous;Carboxylic Acids;Phenyls & Phenyl-Het
Mol File:603-79-2.mol
2,3-Dimethylbenzoic acid Structure
2,3-Dimethylbenzoic acid Chemical Properties
Melting point 144-146 °C (lit.)
Boiling point 271.51°C (estimate)
density 1.0937 (estimate)
refractive index 1.5188 (estimate)
storage temp. Sealed in dry,Room Temperature
pkapKa: 3.771(25°C)
form powder to crystal
color White to Almost white
BRN 971590
CAS DataBase Reference603-79-2(CAS DataBase Reference)
NIST Chemistry ReferenceBenzoic acid, 2,3-dimethyl-(603-79-2)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36-36/37/39-22
WGK Germany 3
RTECS DG8734000
HazardClass IRRITANT
HS Code 29163990
MSDS Information
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2,3-Dimethylbenzoic acid Usage And Synthesis
Chemical Propertieswhite to light yellow crystal powder
Uses2,3-Dimethylbenzoic Acid is used as a reagent in the synthesis of pyridyl benzamides as inhibitors for the kinetoplastid Trypanosoma brucei. 2,3-Dimethylbenzoic Acid is also used as a reagent in the synthesis of 2,3-Dihydro-1H-isoindole-4-carboxylic Acid (D450070) which is a reagent used in the synthesis of aminoalkylbenzoic acid derivatives for the treatment of faintness attacks, hypokinesia, cranial disorders, neurodegenerative disorders, depression, anxiety, neuropathic pain, neuropathological disorders and sleep disorders.
DefinitionChEBI: A dimethylbenzoic acid in which the two methyl groups are located at positions 2 and 3.
General Description2,3-Dimethylbenzoic acid shows high binding affinity with antenna-specific odorant-binding protein of the alfalfa plant bug, Adelphocoris lineolatus.
Purification MethodsCrystallise the acid from EtOH. It is volatile in steam. The amide has m 156o (from H2O). [Beilstein 9 H 531, 9 III 2434, 9 IV 1797.]
2,4-Dimethylbenzoic acid (2,4-dimethylphenyl)methyl ester 4-[3-(2-Chloroethyl)-3-nitrosoureido]-2,6-dimethylbenzoic acid 3-Amino-2,5-dimethylbenzoic acid Ethyl 2-(Chlorosulfonyl)acetate Ascoric Acid 4-bromo-2,6-dimethylbenzoic acid 4-(acetylamino)-2,6-dimethylbenzoic acid 4-Methoxy-2,6-dimethylbenzoic acid methyl ester 4-Benzoyl-3,5-dimethylbenzoic acid ethyl ester 5-(aminosulfonyl)-2,4-dimethylbenzoic acid 4-Nitro-2,6-dimethylbenzoic acid methyl ester 3-Chloro-6-hydroxy-4-methoxy-2,5-dimethylbenzoic acid methyl ester 2-Hydroxy-4-methoxy-3,6-dimethylbenzoic acid 4-carboxy-3-hydroxy-5-methylphenyl ester 4-Hydroxy-2,6-dimethylbenzoic acid 3,5-Dimethylbenzoic acid trimethylsilyl ester 3-Formyl-4,6-dihydroxy-2,5-dimethylbenzoic acid methyl ester 2,6-Dimethylbenzoic acid 4-[bis(2-chloroethyl)amino]phenyl ester 2,4-Dimethylbenzoic acid trimethylsilyl ester

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