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2-methyl-1-phenyl-2,5-dihydro-1H-phosphole 1-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15450-91-6

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15450-91-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15450-91-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,5 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15450-91:
(7*1)+(6*5)+(5*4)+(4*5)+(3*0)+(2*9)+(1*1)=96
96 % 10 = 6
So 15450-91-6 is a valid CAS Registry Number.

15450-91-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-1-phenyl-2,5-dihydro-1λ<sup>5</sup>-phosphole 1-oxide

1.2 Other means of identification

Product number -
Other names 2-methyl-1-phenyl-3-phospholene 1-oxide

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:15450-91-6 SDS

15450-91-6Relevant academic research and scientific papers

Alkylation and cyclopentannulation of phospholene derivatives

Pakulski, Zbigniew,Kwiatosz, Renata,Micha? Pietrusiewicz

, p. 1481 - 1492 (2007/10/03)

The deprotonation of 1-phenyl-3-phospholene 1-oxide, 1-sulfide or 1-borane with 1 or 2 equiv of LDA, followed by quenching with electrophiles gave a range of 2-mono- or 2,5-disubstituted phospholene derivatives in good yield. Only trans substitution in re

Chiral base promoted enantioselective rearrangement of organophosphorus epoxides

Pakulski, Zbigniew,Koprowski, Marek,Pietrusiewicz, K. Micha?

, p. 8219 - 8226 (2007/10/03)

Cinchona alkaloids serve as effective chiral bases for enantioselective rearrangement of 3,4-epoxyphospholane oxides resulting in the formation of P,C-chirogenic 4-hydroxy-2-phospholene derivatives with up to 52% ee. A stereochemical course of the epoxide

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