2-Chloro-4,6-dimethylbenzaldehyde

Base Information

Chemical Name:2-Chloro-4,6-dimethylbenzaldehyde
CAS No.:88174-22-5
Molecular Formula:C9H9ClO
Molecular Weight:168.623
Hs Code.:
DSSTox Substance ID:DTXSID20550572
Wikidata:Q82429985

Synonyms:2-chloro-4,6-dimethylbenzaldehyde;88174-22-5;DTXSID20550572

Suppliers and Price of 2-Chloro-4,6-dimethylbenzaldehyde

Supply Marketing:

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

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Chemical Property of 2-Chloro-4,6-dimethylbenzaldehyde

Chemical Property:

XLogP3:2.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:168.0341926
Heavy Atom Count:11
Complexity:147

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC(=C(C(=C1)Cl)C=O)C

Technology Process of 2-Chloro-4,6-dimethylbenzaldehyde

There total 4 articles about 2-Chloro-4,6-dimethylbenzaldehyde 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: 85.0%

: 15764-16-6
2,4-dimethylbenzaldehyde

: 88174-22-5
2-chloro-4,6-dimethylbenzaldehyde

Guidance literature:: With N-chloro-succinimide; palladium diacetate; silver trifluoroacetate; anthranilic acid; trifluoroacetic acid; In 1,2-dichloro-ethane; at 60 ℃; for 24h; Sealed tube;
DOI:10.1021/acs.orglett.8b03359

Reference yield: 65.0%

: 50817-80-6
2-chloro-4-methyl-benzaldehyde

: potassium trifluoro(methyl)boranuide

: 88174-22-5
2-chloro-4,6-dimethylbenzaldehyde

Guidance literature:: With palladium diacetate; 1-fluoro-2,4,6-trimethylpyridin-1-ium tetrafluoroborate; trifluoroacetic acid; at 90 ℃; for 24h; regioselective reaction; Inert atmosphere; Sealed tube;
DOI:10.1021/jacs.8b00048