2-Cyano-2-(2,3-dimethoxybenzylidene)acetic acid

Base Information

Chemical Name:2-Cyano-2-(2,3-dimethoxybenzylidene)acetic acid
CAS No.:91106-58-0
Molecular Formula:C12H11NO4
Molecular Weight:233.224
Hs Code.:
European Community (EC) Number:663-134-4
Nikkaji Number:J3.658.152B
Wikidata:Q76313773

Synonyms:SCHEMBL7814194;AKOS000148197;J3.658.152B;2-Cyano-3-(2,3-dimethoxyphenyl)propenoic acid;2-CYANO-2-(2,3-DIMETHOXYBENZYLIDENE)ACETIC ACID

Suppliers and Price of 2-Cyano-2-(2,3-dimethoxybenzylidene)acetic acid

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2-Cyano-2-(2,3-dimethoxybenzylidene)acetic acid

Chemical Property:

XLogP3:1.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:4
Exact Mass:233.06880783
Heavy Atom Count:17
Complexity:355

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC=CC(=C1OC)C=C(C#N)C(=O)O
Isomeric SMILES:COC1=CC=CC(=C1OC)/C=C(\C#N)/C(=O)O

Technology Process of 2-Cyano-2-(2,3-dimethoxybenzylidene)acetic acid

There total 4 articles about 2-Cyano-2-(2,3-dimethoxybenzylidene)acetic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 58531-09-2
ethyl 2-cyano-3-(2,3-dimethoxyphenyl)propenoate

: 91106-58-0
2-cyano-3t-(2,3-dimethoxy-phenyl)-acrylic acid

Guidance literature:: With hydrogenchloride; acetic acid;

Reference yield:

: 86-51-1
2,3-dimethyoxybenzaldehyde

: 91106-58-0
2-cyano-3t-(2,3-dimethoxy-phenyl)-acrylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: piperidine

2: glacial acetic acid; concentrated hydrochloric acid

With piperidine; hydrogenchloride; acetic acid;