Carbamic acid, [1-(aminothioxomethyl)cyclopropyl]-, phenylmethyl ester

Base Information

Chemical Name:Carbamic acid, [1-(aminothioxomethyl)cyclopropyl]-, phenylmethyl ester
CAS No.:541528-07-8
Molecular Formula:C₁₂H₁₄N₂O₂S
Molecular Weight:250.321
Hs Code.:
DSSTox Substance ID:DTXSID50457323
Nikkaji Number:J1.864.375H
Wikidata:Q82280135

Synonyms:541528-07-8;Carbamic acid, [1-(aminothioxomethyl)cyclopropyl]-, phenylmethyl ester;DTXSID50457323;1-(Benzyloxycarbonylamino)cyclopropane-1-carbothioamide

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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 Carbamic acid, [1-(aminothioxomethyl)cyclopropyl]-, phenylmethyl ester

Chemical Property:

XLogP3:1.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:250.07759887
Heavy Atom Count:17
Complexity:310

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC1(C(=S)N)NC(=O)OCC2=CC=CC=C2

Technology Process of Carbamic acid, [1-(aminothioxomethyl)cyclopropyl]-, phenylmethyl ester

There total 2 articles about Carbamic acid, [1-(aminothioxomethyl)cyclopropyl]-, phenylmethyl ester 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:

: 108056-97-9
N-(benzyloxycarbonyl)-1-aminocyclopropane-1-carboxamide

: 541528-07-8
benzyl 1-(aminocarbonothioyl)cyclopropylcarbamate

Guidance literature:: With Lawessons reagent; In tetrahydrofuran; at 50 ℃;
DOI:10.1016/S0040-4039(02)02847-2

Reference yield:

: 84677-06-5
(benzyloxycarbonylamino)cyclopropanecarboxylic acid

: 541528-07-8
benzyl 1-(aminocarbonothioyl)cyclopropylcarbamate

Guidance literature:: Multi-step reaction with 2 steps

1: EDCl; NH₄Cl / dimethylformamide

2: Lawesson's reagent / tetrahydrofuran / 50 °C

With Lawessons reagent; ammonium chloride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4039(02)02847-2