96129-66-7

Basic information

• Product Name: methyl 2-(2,5-dichlorophenyl)acetate
• Synonyms: methyl 2-(2,5-dichlorophenyl)acetate
• CAS NO: 96129-66-7
• Molecular Weight: 219.067
• Mol File: 96129-66-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: methyl 2-(2,5-dichlorophenyl)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-(2,5-dichlorophenyl)acetate(96129-66-7)
• EPA Substance Registry System: methyl 2-(2,5-dichlorophenyl)acetate(96129-66-7)

Safety Data

• Hazardous Substances Data: 96129-66-7(Hazardous Substances Data)

Upstream product

• 7664-93-9 sulfuric acid 
• 124-41-4 sodium methylate 
• 67-56-1 methanol 
• 3218-50-6 2-(2,5-dichlorophenyl)acetonitrile 

Downstream Products

• 5398-79-8 2-(2,5-dichlorophenyl)acetic acid 
• 1875-87-2 2,5-dichloro-β-phenethyl alcohol 

Relevant articles and documents

PROTEIN KINASE INHIBITORS AND USES THEREOF FOR THE TREATMENT OF DISEASES AND CONDITIONS

Identified compounds demonstrate protein kinase inhibitory activity. More specifically, the compounds are demonstrated to inhibit receptor interacting kinase 2 (RIPK2) and/or Activin-like kinase 2 (ALK2) and/or receptor interacting kinase 3 (RIPK3). Compounds that are either dual RIPK2/ALK2 inhibitors or that preferentially inhibit RIPK2 or ALK2 or RIPK3 could provide therapeutic benefit. Compounds that function as RIPK3 inhibitors provide therapeutic benefit in the treatment of inflammatory and degenerative conditions.

ANTI-HCMV COMPOSITIONS AND METHODS

This document relates to compounds useful as agents for preventing or treating human cytomegalovirus (HCMV) infections.

Solution and Flash Vacuum Pyrolysis of Some 2,6-Disubstituted β-Phenethylsulfonyl Azides and of β-Styrenesulfonyl Azide

Solution thermolysis of 2,6-dichloro-β-phenethyl- and 2,6-dimethyl-β-phenethylsulfonyl azide leads to the formation of the corresponding 5,8-disubstituted 3,4-dihydro-2,1-benzothiazine 2,2-dioxides resulting from a 1,2-chlorine and -methyl shift, respectively, in the intermediates.No insertion into the phenethyl side chain, or into the side-chain methyl group in the 2,6-dimethyl case, was detected.Attempted cyclization of ethene-sulfonanilides to 2,1-benzothiazine 2,2-dioxide failed.The orientation of the dichlorosultam was established unambiguously by its FVP to 4,7-dichloroindoline and by the synthesis of an authentic sample.Solution thermolysis of β-styrenesulfonyl azide gave only hydrogen abstraction (32) and solvent insertion (33) products, but FVP gave indole, phenylacetonitrile, and phenylacetylene.