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3-Amino-4-methoxybenzoic acid, 98%|128840|2840-26-8

3-Amino-4-methoxybenzoic acid, 98%

Cat. No JK128840_25_G
J&K Chemical

Product Information

Product Name
3-Amino-4-methoxybenzoic acid, 98%
Brand Name
J&K
Product Number
128840
CAS
2840-26-8
Molecular Formula
C8H9NO3
Molecular Weight
167.16
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
3-Amino-p-anisic Acid
PubChem CID
17823
IUPAC Name
3-amino-4-methoxybenzoic acid
InChI Key
FDGAEAYZQQCBRN-UHFFFAOYSA-N
SMILES
COC1=C(C=C(C=C1)C(=O)O)N

Properties

Melting Point
208-210

Safety Information

Signal Word
Warning
Hazard Statement
H315
H319
H335
Precautionary Statement
P280
P321
P261
P271
P319
P405
P501
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References

Enzymatic oligomerization and polymerization of arylamines: state of the art and perspectives
Publication Name: Chemical Papers
Publication Date: 2016-12-19
DOI: 10.1007/s11696-016-0094-3

A nitrous acid biosynthetic pathway for diazo group formation in bacteria.
Publication Name: Nature Chemical Biology
Publication Date: 2015-12-21
DOI: 10.1038/nchembio.1991

Self-doped carboxylated polyaniline: effect of hydrogen bonding on the doping of polymers
Publication Name: Macromolecular Research
Publication Date: 2009-09
DOI: 10.1007/bf03218921

An artificial beta-sheet that dimerizes through parallel beta-sheet interactions
Publication Name: Journal of the American Chemical Society
Publication Date: 2007-10-01
DOI: 10.1021/ja073391r

Diazotization of Aminophenols, Aminonaphthols, Aminobenzenesulfonic Acids, and Aminoarenecarboxylic Acids in Acidic Media
Publication Name: Science of Synthesis
Publication Date: 2007

3-Amino-4-methoxybenzoic acid, 98%

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