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7305-12-6

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7305-12-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7305-12-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,0 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7305-12:
(6*7)+(5*3)+(4*0)+(3*5)+(2*1)+(1*2)=76
76 % 10 = 6
So 7305-12-6 is a valid CAS Registry Number.

7305-12-6SDS

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-(4-nitrophenyl) N,N-dimethylcarbamothioate

1.2 Other means of identification

Product number -
Other names S-4-nitrophenyl thiocarbamate

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:7305-12-6 SDS

7305-12-6Relevant 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.

Microwave-mediated Newman-Kwart rearrangement in water

Hoffmann, Ina,Schatz, Jürgen

, p. 80692 - 80699 (2016/09/09)

For the first time the unimolecular Newman-Kwart rearrangement is performed in pure water. The elevated temperatures required for the 1,3-aryl shift are easily accomplished by microwave irradiation. Differently functionalized substrates underline the expe

The Newman-Kwart rearrangement of O-aryl thiocarbamates: Substantial reduction in reaction temperatures through palladium catalysis

Harvey, Jeremy N.,Jover, Jesus,Lloyd-Jones, Guy C.,Renny, Joseph S.,Moseley, Jonathan D.,Murray, Paul

supporting information; experimental part, p. 7612 - 7615 (2009/12/26)

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