ethyl 2-amino-5-chloro-benzoate hydrochloride

Base Information

Chemical Name:ethyl 2-amino-5-chloro-benzoate hydrochloride
CAS No.:130408-01-4
Molecular Formula:C₉H₁₀ClNO₂*ClH
Molecular Weight:236.098
Hs Code.:

Synonyms:ethyl 5-chloroanthranilate hydrochloride

Suppliers and Price of ethyl 2-amino-5-chloro-benzoate hydrochloride

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

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Chemical Property of ethyl 2-amino-5-chloro-benzoate hydrochloride

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of ethyl 2-amino-5-chloro-benzoate hydrochloride

There total 1 articles about ethyl 2-amino-5-chloro-benzoate hydrochloride 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: 96.0%

: 4743-17-3
5-Chloroisatoic anhydride

: 64-17-5
ethanol

: 130408-01-4
ethyl 5-chloroanthranilate hydrochloride

Guidance literature:: With hydrogenchloride; Ambient temperature;
DOI:10.1021/jm00105a044

Reference yield: 92.0%

: 130408-01-4
ethyl 5-chloroanthranilate hydrochloride

: 5584-15-6
5-chloroanthranilic acid hydrazide

Guidance literature:: With hydrazine hydrate; In ethanol; for 16h; Heating;
DOI:10.1021/jm00105a044

Reference yield:

: 130408-01-4
ethyl 5-chloroanthranilate hydrochloride

: 104615-59-0
5-(2-amino-5-chlorophenyl)-3-phenyl-1H-1,2,4-triazole

Guidance literature:: Multi-step reaction with 2 steps

1: 92 percent / hydrazine hydrate / ethanol / 16 h / Heating

2: 62 percent / chlorobenzene; ethanol / Heating

With hydrazine hydrate; In ethanol; chlorobenzene;
DOI:10.1021/jm00105a044