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3,5-Dimethoxyaniline, 98%|251968|10272-07-8

3,5-Dimethoxyaniline, 98%

Cat. No JK251968_5_G
J&K Chemical

Product Information

Product Name
3,5-Dimethoxyaniline, 98%
Brand Name
J&K
Product Number
251968
CAS
10272-07-8
Molecular Formula
C8H11NO2
Molecular Weight
153.18
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
5-Aminoresorcinol dimethyl ether
PubChem CID
66301
IUPAC Name
3,5-dimethoxyaniline
InChI Key
WNRGWPVJGDABME-UHFFFAOYSA-N
SMILES
COC1=CC(=CC(=C1)N)OC

Properties

Melting Point
54-57
Boiling Point
178
Flash Point
135

Safety Information

Signal Word
Warning
Hazard Statement
H302
H315
H319
H335
Precautionary Statement
P270
P330
P501
P280
P321
P261
P271
P319
P405
P301+P317
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References Data Source From Pubchem

Trifluoromethyl–pyrazole–carboxamides as COX inhibitors: synthesis, microed structural analysis, computational profiling, and biological evaluation
Publication Name: BMC Chemistry
Publication Date: 2025-10-29
DOI: 10.1186/s13065-025-01659-z

Synthesis, biologic properties, and molecular modeling studies of bis-indole based thiosemicarbazones
Publication Name: Monatshefte für Chemie - Chemical Monthly
Publication Date: 2024-07-29
DOI: 10.1007/s00706-024-03230-3

Design, Synthesis and Biological Evaluation of Amide Derivatives of Thiazole-Indole-Isoxazoles as Anticancer Agents
Publication Name: Pharmaceutical Chemistry Journal
Publication Date: 2024-02
DOI: 10.1007/s11094-024-03073-6

Synthesis from 2,2′-Dibromobenzophenone and Primary Amines
Publication Name: Science of Synthesis
Publication Date: 2024

Open science discovery of potent noncovalent SARS-CoV-2 main protease inhibitors
Publication Name: Science (New York, N.Y.)
Publication Date: 2023-11-10
DOI: 10.1126/science.abo7201

3,5-Dimethoxyaniline, 98%

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