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21612-82-8

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21612-82-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21612-82-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,6,1 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 21612-82:
(7*2)+(6*1)+(5*6)+(4*1)+(3*2)+(2*8)+(1*2)=78
78 % 10 = 8
So 21612-82-8 is a valid CAS Registry Number.

21612-82-8SDS

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 imino(triphenyl)-$l^{5}-phosphane,hydrochloride

1.2 Other means of identification

Product number -
Other names Aminotriphenylphosphoniumchlorid

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:21612-82-8 SDS

21612-82-8Relevant articles and documents

Synthesis and characterization of some phosphazenium chloride salts, [R3PNH2]+Cl- (R = phenyl, p-chlorophenyl and morpholino)

Sivaramakrishna, Akella,Rao, M. N. Sudheendra

, p. 147 - 149 (2011)

Some phosphazenium chloride salts of the type [R3PNH 2]+Cl-, where R = phenyl, p-chlorophenyl and morpholino, were synthesized by the reaction of the corresponding phosphiniminocyclotrithiazene compounds (R3PNS

Cyclic sulphur-nitrogen compounds and phosphorus reagents: Part XIII-Reactions of cyclic sulphur-nitrogen chlorides with Ph3P-influences of tetiary base, Et3N and the ring size of the cyclothiazyl chloride on the product formation

Mohan, T.,Senthivel, P.,Rao, M. N. Sudheendra

, p. 961 - 966 (2007/10/03)

Similar to the reactions with S4N3Cl and S3N3Cl3, triphenylphosphine reacts with five-membered cyclic sulphur-nitrogen chlorides namely, S3N2Cl and S3N2Cl2 to give triphenylphosphiniminium chloride, Ph3P=NH+2Cl- as the major product.Maximum yield (ca. 90percent) is obtained when triphenylphosphine is reacted with S3N2Cl in acetonitrile at room temperature in 2 : 1 molar ratio.Analogous reactions performed in presence of triethylamine afford two cyclothiazene products containing phosphinimino substituent.The ring size of the S - N chloride seems to determine the nature of phosphiniminocyclothiazenes formed.A rationalization of the results obtained has been attempted.

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