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2H-Pyrrole, 2,2-dimethyl-3,5-diphenyl-, 1-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72700-88-0

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72700-88-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72700-88-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,7,0 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 72700-88:
(7*7)+(6*2)+(5*7)+(4*0)+(3*0)+(2*8)+(1*8)=120
120 % 10 = 0
So 72700-88-0 is a valid CAS Registry Number.

72700-88-0SDS

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 2,2-dimethyl-1-oxido-3,5-diphenylpyrrol-1-ium

1.2 Other means of identification

Product number -
Other names 2,2-Dimethyl-3,5-dipphenyl-2H-pyrrol-1-oxid

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:72700-88-0 SDS

72700-88-0Downstream Products

72700-88-0Relevant academic research and scientific papers

Nitrones and Oxaziridines. XL Oxidation of 2H-Pyrroles and 3-Benzoyloxy-1-pyrrolines

Black, David St.C.,Strauch, Richard J.

, p. 699 - 707 (2007/10/02)

Peracid oxidation of 2H-pyrroles (1a-d) gave the related 2H-pyrrole 1-oxides (2a-d).Similar oxidation of the 3-benzoyloxy-1-pyrroline (7a) also gave a 2H-pyrrole 1-oxide (9), while other benzoyloxy pyrrolines (7b,c) yielded the related oxaziridines (8b,c)

2H-PYRROLE-1-OXIDES BY SELENIUM DIOXIDE DEHYDROGENATION OF PYRROLINE-1-OXIDES

Bender, H.,Doepp, D.

, p. 1833 - 1836 (2007/10/02)

Five different 2H-pyrrole-1-oxides have been prepared by dehydrogenation of their corresponding pyrroline-1-oxide precursors and characterized by 1,3-dipolar cycloadditions with dimethyl ethyne dicarboxylate and/or N-phenyl maleic imide.

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