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39078-86-9

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39078-86-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39078-86-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,0,7 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 39078-86:
(7*3)+(6*9)+(5*0)+(4*7)+(3*8)+(2*8)+(1*6)=149
149 % 10 = 9
So 39078-86-9 is a valid CAS Registry Number.

39078-86-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name S-Benzyl-N-methylthiocarbamate

1.2 Other means of identification

Product number -
Other names methyl-thiocarbamic acid S-benzyl 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:39078-86-9 SDS

39078-86-9Relevant articles and documents

Visible-light-promoted synthesis of secondary and tertiary thiocarbamates from thiosulfonates andN-substituted formamides

Bi, Wen-Zhu,Zhang, Wen-Jie,Li, Zi-Jie,He, Yuan-Hao,Feng, Su-Xiang,Geng, Yang,Chen, Xiao-Lan,Qu, Ling-Bo

, p. 8701 - 8705 (2021/10/22)

A general visible-light-promoted metal-free synthesis of secondary and tertiary thiocarbamates starting from thiosulfonates andN-substituted formamides is developed. By employing rhodamine B as a photocatalyst andtert-butyl hydroperoxide (TBHP) as an oxidant, a wide scope of thiocarbamates can be obtained through direct thiolation of acyl C-H bonds under irradiation of blue light at room temperature for 12 h.

Dithioallophanic Acids : Interaction of Carbon Oxysulphide with S-Benzyl-N-methylisothiocarbamide

Dravid, R. N.,Chande, M. S.

, p. 496 - 498 (2007/10/02)

Carbon oxysulphide reacts with S-benzyl-N-methylisothiocarbamide in cold benzene to afford products which are different from those obtained earlier in similar reactions.Methylthiocarbamide and thiocyanic acid adduct, an interesting product has been isolated.In addition to this S-benzyl-N-methylthiocarbamate, S-benzyl-N-methyldithiocarbamate and dibenzyl disulphide have also been isolated from the reaction mixture.The formation of these products from dithioallophanic acid intermediate is rationalised.

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