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37174-63-3

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37174-63-3 Usage

Description

S-METHYL-N,N-DIETHYLTHIOCARBAMATE, also known as S-Methyl N,N-Diethylthiocarbamate (CAS# 37174-63-3), is an organic compound with a chemical structure that features a thiocarbonyl group attached to a methyl and two diethyl groups. It is characterized by its yellow oil appearance and is known for its utility in various organic synthesis processes.

Uses

Used in Organic Synthesis:
S-METHYL-N,N-DIETHYLTHIOCARBAMATE is used as a synthetic intermediate for the production of various organic compounds. Its unique chemical structure allows it to participate in a range of reactions, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, S-METHYL-N,N-DIETHYLTHIOCARBAMATE is used as a building block for the development of new drugs. Its reactivity and functional groups enable the creation of novel molecular structures with potential therapeutic applications.
Used in Agrochemical Industry:
S-METHYL-N,N-DIETHYLTHIOCARBAMATE is also utilized in the agrochemical industry for the synthesis of pesticides and other crop protection agents. Its role in creating new molecules with improved efficacy and selectivity contributes to the development of more effective and environmentally friendly products.
Used in Research and Development:
In the field of research and development, S-METHYL-N,N-DIETHYLTHIOCARBAMATE serves as a key compound for exploring new chemical reactions and understanding the underlying mechanisms. Its versatility in organic synthesis makes it an essential tool for chemists working on innovative projects and advancing scientific knowledge.

Check Digit Verification of cas no

The CAS Registry Mumber 37174-63-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,1,7 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 37174-63:
(7*3)+(6*7)+(5*1)+(4*7)+(3*4)+(2*6)+(1*3)=123
123 % 10 = 3
So 37174-63-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H13NOS/c1-4-7(5-2)6(8)9-3/h4-5H2,1-3H3

37174-63-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name S-Methyl N,N-Diethylthiocarbamate

1.2 Other means of identification

Product number -
Other names S-methyl N,N-diethylcarbamothioate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:37174-63-3 SDS

37174-63-3Relevant articles and documents

O,S-Dimethyl carbonodithioate as a phosgene substitute for the preparation of S-methyl alkylcarbamothioates and dialkylcarbamothioates

Degani, Iacopo,Fochi, Rita,Magistris, Claudio

experimental part, p. 3807 - 3818 (2010/03/30)

O,S-Dimethyl carbonodithioate is proposed as a suitable and safely handled reagent that can be used as a replacement for phosgene in the synthesis of S-methyl alkyl- and dialkylcarbamothioates. The former were obtained by a two-step procedure, which can also be carried out in a one-pot fashion without isolating the intermediates O-methyl alkylcarbamothioates; the overall yields of the pure S-methyl alkylcarbamothioates were 94-98%. Optimal conditions for the synthesis of S-methyl dialkylcarbamothioates involved a one-step procedure in a solvent-free system in the presence of triethyl(methyl)ammonium methyl carbonate as a catalyst; yields of the pure products were 85-98%. A mechanism is proposed for the carbamothioate-formation reaction. Georg Thieme Verlag Stuttgart.

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