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2H-Pyrrole, 3,4-dihydro-4,5-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

155220-56-7

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155220-56-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 155220-56-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,2,2 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 155220-56:
(8*1)+(7*5)+(6*5)+(5*2)+(4*2)+(3*0)+(2*5)+(1*6)=107
107 % 10 = 7
So 155220-56-7 is a valid CAS Registry Number.

155220-56-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-diphenyl-3,4-dihydro-2H-pyrrole

1.2 Other means of identification

Product number -
Other names 2H-Pyrrole,3,4-dihydro-4,5-diphenyl

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:155220-56-7 SDS

155220-56-7Downstream Products

155220-56-7Relevant academic research and scientific papers

Application of the thioimidate cyclopropane rearrangement to heterocyclic synthesis. Preparation of diaryl pyrrolines

Chang, Ronald K.,Dipardo, Robert M.,Kuduk, Scott D.

, p. 8513 - 8516 (2005)

Substituent effects on the thioimidate cyclopropane rearrangement and factors affecting regioselectivity are reported. Palladium-mediated coupling of the pyrrolothiomethylimidate rearrangement products with Grignard reagents provides diaryl pyrrolines in

A General Stereocontrolled Synthesis of cis-2,3 Disubstituted Pyrrolidines and Piperidines

Pal, Kollol,Behnke, Mark L.,Tong, Liang

, p. 6205 - 6208 (2007/10/02)

A general synthetic method is reported for the preparation of cis-2,3-disubstituted pyrrolidines and piperidines from readily available acyclic precursors.The key reaction involves the stereoselective reduction of a cyclic imine controlled by the C-3 subs

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