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3052-73-1

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3052-73-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3052-73-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,5 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3052-73:
(6*3)+(5*0)+(4*5)+(3*2)+(2*7)+(1*3)=61
61 % 10 = 1
So 3052-73-1 is a valid CAS Registry Number.

3052-73-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name phenyl N,N-diethyldithiocarbamate

1.2 Other means of identification

Product number -
Other names diethyl-dithiocarbamic acid phenyl ester

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:3052-73-1 SDS

3052-73-1Relevant articles and documents

Aryne Three-Component Coupling Involving CS2for the Synthesis of S-Aryl Dithiocarbamates

Bhattacharjee, Subrata,Deswal, Shiksha,Manoj, Niket,Jindal, Garima,Biju, Akkattu T.

supporting information, p. 9083 - 9088 (2021/11/30)

A facile synthesis of biologically important S-aryl dithiocarbamates has been demonstrated by the aryne three-component coupling involving CS2 and aliphatic amines. This transition-metal-free and mild reaction is scalable and operates with good functional group compatibility. Preliminary mechanistic experiments, including density functional theory studies, are also provided. Moreover, with 3-triflyloxybenzynes, a unique four-component coupling incorporating tetrahydrofuran was observed.

Chemoselective C–S/S–S Formation between Diaryl Disulfides and Tetraalkylthiuram Disulfides

Peng, Kang,Zhu, Hui,Liu, Xing,Peng, Han-Ying,Chen, Jin-Quan,Dong, Zhi-Bing

, p. 7629 - 7634 (2019/12/03)

An efficient C–S/S–S formation for the chemoselective synthesis of aryl dithiocarbamate (C–S formation) and aryl dialkylcarbamo(dithioperoxo)thioate (S–S formation) was studied. The chemoselectivity could be controlled by modulating the reaction temperature, base, and catalyst. The transformation features a simple reaction, easily available starting materials, high selectivity and easy performance, showing its practical synthetic value for the preparation of some potential biologically or pharmaceutically active compounds.

Synthesis of Phenyl Dithiocarbamates Starting from Sodium Dialkyldithiocarbamates and Aryl Boronic Acids: a Copper Catalyzed S-Arylation

Gao, Ming-Yuan,Xu, Wan,Zhang, Shi-Bo,Li, Yue-Sheng,Dong, Zhi-Bing

, p. 6693 - 6698 (2018/11/25)

A convenient and efficient protocol for the S-arylation of sodium dialkyldithiocarbamates was developed. With the catalysis of copper(I) bromide, sodium dialkyldithiocarbamates coupled with aryl boronic acids giving the C-S coupling products smoothly in g

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