3,5-Dimethoxybenzoic acid

3,5-Dimethoxybenzoic acid Basic information
Product Name:3,5-Dimethoxybenzoic acid
Synonyms:3,5-DIMETHOXYBENZOIC ACID;AKOS 227-39;AKOS BBS-00007826;AURORA 8636;OTAVA-BB BB7013191651;RARECHEM AL BO 0044;TIMTEC-BB SBB007798;3,5-dimethoxy-benzoicaci
CAS:1132-21-4
MF:C9H10O4
MW:182.17
EINECS:214-473-8
Product Categories:FINE Chemical & INTERMEDIATES;Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Benzoic acid;Organic acids;Building Blocks for Dendrimers;Functional Materials;C9;Carbonyl Compounds;Carboxylic Acids;bc0001
Mol File:1132-21-4.mol
3,5-Dimethoxybenzoic acid Structure
3,5-Dimethoxybenzoic acid Chemical Properties
Melting point 178-180 °C (lit.)
Boiling point 275.56°C (rough estimate)
density 1.2481 (rough estimate)
refractive index 1.4500 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility almost transparency in hot Methanol
form Crystalline Powder
pka3.96±0.10(Predicted)
color Almost white to light beige-pink
BRN 511834
InChIKeyIWPZKOJSYQZABD-UHFFFAOYSA-N
LogP2.190
CAS DataBase Reference1132-21-4(CAS DataBase Reference)
NIST Chemistry Reference3,5-Dimethoxybenzoic acid(1132-21-4)
EPA Substance Registry SystemBenzoic acid, 3,5-dimethoxy- (1132-21-4)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
Hazard Note Irritant
TSCA Yes
HS Code 29189090
MSDS Information
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3,5-Dimethoxybenzoic acid English
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3,5-Dimethoxybenzoic acid Usage And Synthesis
Chemical Propertiesalmost white to light beige-pink cryst. powder
Uses3,5-Dimethoxybenzoic acid (3,5-DmeoxBA) can be used as a reactant for the synthesis of:
  • 5,7-Dimethoxy-3,4-diphenylisocoumarin by coupling with diphenylacetylene.
  • Biotin dimedone, a reagent used in the study of protein sulfenation.

It can also be used as a ligand to synthesize lanthanide complexes [Ln(3,5-DmeoxBA)3(phen)]2; where phen is 1,10-phenanthroline.
DefinitionChEBI: 3,5-dimethoxybenzoic acid is a methoxybenzoic acid that is benzoic acid which is substituted by methoxy groups at positions 3 and 5. It has a role as a plant metabolite. It is a conjugate acid of a 3,5-dimethoxybenzoate.
Purification MethodsCrystallise the acid from water, EtOH or aqueous acetic acid and dry it in a vacuum. [Beilstein 10 H 405, 10 I 195, 10 III 1446, 10 IV 1501.]
2-Methoxybenzoic acid 2-{[(acetylamino)acetyl]amino}-4,5-dimethoxybenzoic acid Methyl syringate 2-[(2-ETHYLBUTANOYL)AMINO]-4,5-DIMETHOXYBENZOIC ACID 3,4,5-TRIACETOXYBENZOIC ACID 3,4-Dimethoxybenzoic acid 2-hydroxy-3-methylphenyl ester 3,4,5-TRIMETHOXYBENZOIC ANHYDRIDE 2-Amino-4,5-dimethoxybenzoic acid ethyl ester METHYL-2-ISOCYANO-4,5-DIMETHOXYBENZOIC ACID 3,4,5-TRIMETHOXY-2-NITROBENZOIC ACID Ascoric Acid HYDROXY-3,4-DIMETHOXYBENZOIC ACID, 2- 4-ACETOXY-3,5-DIMETHOXYBENZOIC ACID Methyl 2-amino-3,4,5-trimethoxybenzoate 3-BROMO-5-CHLORO-2,6-DIMETHOXYBENZOIC ACID 4-ETHOXYCARBONYLOXY-3,5-DIMETHOXYBENZOIC ACID 8-(DIETHYLAMINO)OCTYL 3,4,5-TRIMETHOXYBENZOATE HYDROCHLORIDE Benzoic acid-3-hydroxy-4,5-dimethoxy- methyl ester

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