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111830-18-3

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111830-18-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111830-18-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,8,3 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 111830-18:
(8*1)+(7*1)+(6*1)+(5*8)+(4*3)+(3*0)+(2*1)+(1*8)=83
83 % 10 = 3
So 111830-18-3 is a valid CAS Registry Number.

111830-18-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-ethyl-5,5-dimethyl-N-phenyl-1,3,2-dioxaphosphinan-2-amine

1.2 Other means of identification

Product number -
Other names 1,3,2-Dioxaphosphorinan-2-amine,N-ethyl-5,5-dimethyl-N-phenyl

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:111830-18-3 SDS

111830-18-3Relevant articles and documents

Nature of acid-catalyzed alcoholysis of amides of trivalent-phosphorus acids

Nifantyev,Gratchev,Burmistrov Yu.,Vasyanina

, p. 9839 - 9860 (2007/10/02)

To study the chemical nature of the acid catalysis of amides of trivalent-phosphorus acids (ATPA) alcoholysis the most important procedural problems have been solved. Simple and efficacious techniques for the purification of original ATPA from amine hydrohalides have been worked out. A precise and reliable way has been chosen to control the residual amount of amine hydrohalides in ATPA having been subjected to the various purification procedures. The nature of the dependence of alcoholysis rate constants for ATPA of different structures on the amine-hydrohalide concentration has been established. The general acid catalysis was established using the Bronsted equation, so that the process includes the formation of a catalytic H-complex incorporating substrate and catalyst on the whole. Amides P(III) of different types treated with anhydrous hydroborofluoric acid readily from the corresponding P-protonated salts. The conversions of corresponding products of complete protonation have been investigated. The structure of P-protonated salt 23 has been studied by means of X-ray analysis.

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