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(2E,4E)-4-Methyl-2,3-diphenyl-1-pyrrolidin-1-yl-hepta-2,4-diene-1,6-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75476-16-3

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75476-16-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75476-16-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,4,7 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 75476-16:
(7*7)+(6*5)+(5*4)+(4*7)+(3*6)+(2*1)+(1*6)=153
153 % 10 = 3
So 75476-16-3 is a valid CAS Registry Number.

75476-16-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-2,3-diphenyl-1-(pyrrolidin-1-yl)hepta-2,4-diene-1,6-dione

1.2 Other means of identification

Product number -
Other names -

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:75476-16-3 SDS

75476-16-3Downstream Products

75476-16-3Relevant academic research and scientific papers

Reaction of Diphenylcyclopropenone with Primary and Secondary Enaminones. Synthetic and Mechanistic Implications

Kascheres, Concetta,Kascheres, Albert,Pilli, Paula S. H.

, p. 5340 - 5343 (2007/10/02)

Diphenylcyclopropenone (1) reacts with the primary and secondary acyclic enaminones 6a-c in toluene at reflux to afford the 1,5-dihydro-2H-pyrrol-2-ones 7a-c in good yield.The reaction of the primary cyclic enaminone 13a produces a 1,5-dihydro-4H-pyrrol-4-one 14, while the secondary cyclic enaminone 13b yields a 2:1 product (16b) as the principal cycloadduct.Mechanisms are discussed.

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