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1,3,2-Oxazaphospholidine, 2-chloro-3-phenyl-, 2-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38463-52-4

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38463-52-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38463-52-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,6 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 38463-52:
(7*3)+(6*8)+(5*4)+(4*6)+(3*3)+(2*5)+(1*2)=134
134 % 10 = 4
So 38463-52-4 is a valid CAS Registry Number.

38463-52-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-3-phenyl-[1,3,2]oxazaphospholidine 2-oxide

1.2 Other means of identification

Product number -
Other names 2-Chlor-2-oxo-3-phenyl-1,3,2-oxaazaphospholan

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:38463-52-4 SDS

38463-52-4Relevant academic research and scientific papers

Reactions of tert-Butyl Phosphoramidites with Carbon Tetrachloride and Chloroform

Sal'keeva,Nurmaganbetova,Kurmanaliev

, p. 533 - 535 (2007/10/03)

The reactions of 2-tert-butoxy-3-phenyl-1,3,2-oxazaphospholane and di-tert-butyl diethylphosphoramidite with carbon tetrachloride and chloroform were studied. These reactions proceed via formation of an intermediate quasiphosphonium compound. In the proce

Imide-amide rearrangement of cyclic phosphorimidates: A mechanistic study

Cabrita, Eurico J.,Afonso, Carlos A. M.,Gil De Oliveira Santos, Antonio

, p. 1455 - 1467 (2007/10/03)

Studies aimed at the development of new synthetic pathways for the preparation of chiral cyclic oxaza and diaza phosphoramides suitable for use in asymmetric chemistry led us to the investigation of the imide-amide rearrangement of cyclic phosphorimidates

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