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Carbamodithioic acid, ethylphenyl-, phenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62604-37-9

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62604-37-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62604-37-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,6,0 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 62604-37:
(7*6)+(6*2)+(5*6)+(4*0)+(3*4)+(2*3)+(1*7)=109
109 % 10 = 9
So 62604-37-9 is a valid CAS Registry Number.

62604-37-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name phenyl N-ethyl-N-phenylcarbamodithioate

1.2 Other means of identification

Product number -
Other names Aethyl-phenyl-dithiocarbamidsaeure-phenylester

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:62604-37-9 SDS

62604-37-9Downstream Products

62604-37-9Relevant academic research and scientific papers

Copper-mediated coupling of boronic acids, amines, and carbon disulfide: An approach to organic dithiocarbamates

Qi, Chaorong,Guo, Tianzuo,Xiong, Wenfang

supporting information, p. 2626 - 2630 (2016/11/11)

An efficient copper-mediated three-component coupling reaction of boronic acids, amines, and carbon disulfide has been developed, which provides a new approach to a wide range of functionalized dithiocarbamates in good to excellent yields. The present methodology has many advantages, such as mild reaction conditions, easily available substrates, wide substrate scope, and high functional-group tolerance.

A method for the synthesis of thio-carbamate

-

Paragraph 0140; 0141; 0142; 0143; 0144; 0145; 0146-0148, (2016/10/10)

The invention belongs to the technical field of chemical synthesis and discloses a dithiocarbamate synthesis method. The dithiocarbamate synthesis method comprises that in an organic solvent, Ar-B(OH)2, NHR1R2 and carbon disulfide as raw materials and a copper salt and alkali as promoters undergo a reaction at a temperature of 60-120 DEG C for 10-24h with stirring, after the reaction, the reaction product is cooled to a room temperature, then is filtered and then is subjected to reduced pressure distillation for solvent removal so that a crude product is obtained, and the crude product is purified by column chromatography so that dithiocarbamate is obtained. The dithiocarbamate synthesis method realizes dithiocarbamate synthesis by one step, has simple and easy processes and a high product yield, utilizes cheap and easily available raw materials, has a low synthesis cost and has great industrial production values.

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