2-(4-Amino-2-chlorophenyl)ethanethioamide

Base Information

Chemical Name:2-(4-Amino-2-chlorophenyl)ethanethioamide
CAS No.:848133-05-1
Molecular Formula:C₈H₉ClN₂S
Molecular Weight:200.692
Hs Code.:
DSSTox Substance ID:DTXSID101282345

Synonyms:848133-05-1;DTXSID101282345;4-Amino-2-chlorobenzeneethanethioamide

Suppliers and Price of 2-(4-Amino-2-chlorophenyl)ethanethioamide

Supply Marketing:

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

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Chemical Property of 2-(4-Amino-2-chlorophenyl)ethanethioamide

Chemical Property:

XLogP3:1.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:200.0174972
Heavy Atom Count:12
Complexity:174

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC(=C(C=C1N)Cl)CC(=S)N

Technology Process of 2-(4-Amino-2-chlorophenyl)ethanethioamide

There total 1 articles about 2-(4-Amino-2-chlorophenyl)ethanethioamide 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: 56.0%

: 89277-99-6
(2-Chloro-4-nitrophenyl)acetonitrile

: 848133-05-1
2-(4-amino-2-chlorophenyl)ethanethioamide

Guidance literature:: With hydrogen sulfide; triethylamine; In N,N-dimethyl-formamide; at 80 ℃; for 16h;
DOI:10.1021/jm040159c

Reference yield: 95.0%

: 70-11-1
α-bromoacetophenone

: 848133-05-1
2-(4-amino-2-chlorophenyl)ethanethioamide

: 3-chloro-4-[(4-phenyl-1,3-thiazol-2-yl)methyl]aniline HBr salt

Guidance literature:: In ethanol; for 3h; Heating;
DOI:10.1021/jm040159c

Reference yield:

: 848133-05-1
2-(4-amino-2-chlorophenyl)ethanethioamide

: 4-[3-chloro-4-(4-phenyl-thiazol-2-ylmethyl)-phenylamino]-7-methoxy-6-nitro-quinoline-3-carbonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: 95 percent / ethanol / 3 h / Heating

2: pyridine hydrochloride / propan-2-ol / 8 h / Heating

With pyridine hydrochloride; In ethanol; isopropyl alcohol;
DOI:10.1021/jm040159c