Cas 1430270-75-9,(E)-4-benzylidene-N-(tert-butyl)-2-(4-chlorobenzoyl)-1-(4-chlorophenyl)-5-oxopyrrolidine-2-carboxamide

1430270-75-9

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Basic information

Product Name: (E)-4-benzylidene-N-(tert-butyl)-2-(4-chlorobenzoyl)-1-(4-chlorophenyl)-5-oxopyrrolidine-2-carboxamide
Synonyms: (E)-4-benzylidene-N-(tert-butyl)-2-(4-chlorobenzoyl)-1-(4-chlorophenyl)-5-oxopyrrolidine-2-carboxamide
CAS NO:1430270-75-9
Molecular Formula:
Molecular Weight: 521.443
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (E)-4-benzylidene-N-(tert-butyl)-2-(4-chlorobenzoyl)-1-(4-chlorophenyl)-5-oxopyrrolidine-2-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: (E)-4-benzylidene-N-(tert-butyl)-2-(4-chlorobenzoyl)-1-(4-chlorophenyl)-5-oxopyrrolidine-2-carboxamide(1430270-75-9)
EPA Substance Registry System: (E)-4-benzylidene-N-(tert-butyl)-2-(4-chlorobenzoyl)-1-(4-chlorophenyl)-5-oxopyrrolidine-2-carboxamide(1430270-75-9)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
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Hazardous Substances Data: 1430270-75-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1430270-75-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,0,2,7 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1430270-75:
(9*1)+(8*4)+(7*3)+(6*0)+(5*2)+(4*7)+(3*0)+(2*7)+(1*5)=119
119 % 10 = 9
So 1430270-75-9 is a valid CAS Registry Number.

1430270-75-9Upstream product

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1430270-75-9Relevant academic research and scientific papers

One-pot synthesis of 5-oxopyrrolidine-2-carboxamides via a tandem Ugi 4CC/SN cyclization starting from Baylis-Hillman bromides

Zeng, Xiao-Hua,Wang, Hong-Mei,Wu, Lei,Ding, Ming-Wu

, p. 3823 - 3828 (2013)

A one-pot base-mediated synthesis of 5-oxopyrrolidine-2-carboxamides was developed. The reaction of Baylis-Hillman bromides 1, primary amines 2, isocyanides 3 and arylglyoxals 4 produced the 5-oxopyrrolidine-2-carboxamides 6 in good yields via a tandem Ugi condensation and intramolecular substitution at room temperature in the presence of Cs2CO3.

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