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BUTYL-N-PHENYLDITHIOCARBAMATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14549-44-1

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14549-44-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14549-44-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,5,4 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14549-44:
(7*1)+(6*4)+(5*5)+(4*4)+(3*9)+(2*4)+(1*4)=111
111 % 10 = 1
So 14549-44-1 is a valid CAS Registry Number.

14549-44-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name butyl N-phenylcarbamodithioate

1.2 Other means of identification

Product number -
Other names Butylphenyldithiocarbamate

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:14549-44-1 SDS

14549-44-1Relevant academic research and scientific papers

A mild radical method for the dimerization of dithiocarbamates

Chen, Ning,Zhong, Xin,Li, Pingfan,Xu, Jiaxi

supporting information, p. 802 - 809 (2015/02/19)

A general, practical, and efficient method for the dimerization of dithiocarbamates has been developed that can be used to prepare the corresponding bis(1-arylimino-1-alkyl/ arylthiomethyl) disulfides with dilauroyl peroxide (DLP) as mild oxidant. Notably, a lauroyl radical, rather than an undecyl radical, was established as the radical hydrogen-ab- stractor during the dimerization process. The amount of DLP impacts the dimerization yield, with 50 mol-% DLP giving the disulfides in the highest yields. The use of an excess of DLP generates the undecyl radical, which decomposes the disulfides rapidly to the corresponding isothiocyanates.

(S-Butyldithiocarbanilato)copper(I), Cu. Preparation and crystal structure

Willemse, J.,Bosman, W. P.,Noordik, J. H.,Cras, J. A.

, p. 477 - 479 (2007/10/02)

The preparation and the crystal structure of a copper(I) complex with the deprotoned S-Butyldithiocarbanilic ester is described.The crystals of Cu are rhombohedral with one hexameric unit in the unit cell.

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