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2150-31-4

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2150-31-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2150-31-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,5 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2150-31:
(6*2)+(5*1)+(4*5)+(3*0)+(2*3)+(1*1)=44
44 % 10 = 4
So 2150-31-4 is a valid CAS Registry Number.

2150-31-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Phenylthiocarbamidsaeure-O-isopropylester

1.2 Other means of identification

Product number -
Other names Phenylthiocarbamidsaeure-O-<4-methoxy-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:2150-31-4 SDS

2150-31-4Relevant articles and documents

An Fe3O4@SiO2/Schiff base/Cu(ii) complex as an efficient recyclable magnetic nanocatalyst for selective mono: N-arylation of primary O-alkyl thiocarbamates and primary O-alkyl carbamates with aryl halides and arylboronic acids

Sardarian, Ali Reza,Dindarloo Inaloo, Iman,Zangiabadi, Milad

, p. 8557 - 8565 (2019/06/14)

An efficient, convenient and novel method for the selective mono N-arylation of primary O-alkyl thiocarbamates and primary O-alkyl carbamates with aryl halides and arylboronic acids in the presence of a recyclable magnetic Cu(ii) nanocatalyst is described. A variety of mono N-arylated O-alkyl thiocarbamates and O-alkyl carbamates were prepared in good to excellent yields with a broad range of aryl coupling partners. The magnetic nanocatalyst can be easily recovered with an external magnetic field and reused at least five times without noticeable leaching or loss of its catalytic activity. This cost-effective and eco-friendly methodology has some other advantages, such as easy preparation of the catalyst, simple workup procedure, and easy purification, which makes this protocol interesting for the users in various fields of pharmacology and biotechnology systems.

Triorganophosphinegold(I) Carbonimidothioates

Hall, Veronica J.,Siasios, George,Tiekink, Edward R. T.

, p. 561 - 570 (2007/10/02)

The title compounds, R3PAuSC(=NPh)OR', R = Et, Ph or Cy and R' = Me, Et, Pr, Pri or Cy, have been prepared and characterized by spectroscopic methods (i.r., 1H and 13C n.m.r. and f.a.b. m.s.) and, in the case of the R = Ph and R'= Me compound,

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