Cas 1372422-91-7,diethyl 1-acetyl-4-benzoyl-5-benzyl-3-phenyl-1H-pyrrole-2,2(3H)-dicarboxylate

1372422-91-7

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Basic information

Product Name: diethyl 1-acetyl-4-benzoyl-5-benzyl-3-phenyl-1H-pyrrole-2,2(3H)-dicarboxylate
Synonyms: diethyl 1-acetyl-4-benzoyl-5-benzyl-3-phenyl-1H-pyrrole-2,2(3H)-dicarboxylate
CAS NO:1372422-91-7
Molecular Formula:
Molecular Weight: 525.601
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: diethyl 1-acetyl-4-benzoyl-5-benzyl-3-phenyl-1H-pyrrole-2,2(3H)-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: diethyl 1-acetyl-4-benzoyl-5-benzyl-3-phenyl-1H-pyrrole-2,2(3H)-dicarboxylate(1372422-91-7)
EPA Substance Registry System: diethyl 1-acetyl-4-benzoyl-5-benzyl-3-phenyl-1H-pyrrole-2,2(3H)-dicarboxylate(1372422-91-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1372422-91-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1372422-91-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,2,4,2 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1372422-91:
(9*1)+(8*3)+(7*7)+(6*2)+(5*4)+(4*2)+(3*2)+(2*9)+(1*1)=147
147 % 10 = 7
So 1372422-91-7 is a valid CAS Registry Number.

1372422-91-7Upstream product

1372422-91-7Downstream Products

1372422-91-7Relevant academic research and scientific papers

DBU-catalyzed tandem additions of electron-deficient 1,3-conjugated enynes with 2-aminomalonates: A facile access to highly substituted 2-pyrrolines

Yu, Xiuzhao,Zhou, Guanghua,Zhang, Junliang

, p. 4002 - 4004 (2012)

An efficient, metal free approach to highly substituted 2-pyrrolines by DBU-catalyzed tandem additions (a formal [3+2] cycloaddition) of electron-deficient 1,3-conjugated enynes and 2-aminomalonates under mild conditions was developed.

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