Cas 132375-23-6,2-({Cyano-[3-methyl-5-oxo-1-phenyl-1,5-dihydro-pyrazol-(4Z)-ylidene]-methyl}-amino)-propionic acid ethyl ester

132375-23-6

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Basic information

Product Name: 2-({Cyano-[3-methyl-5-oxo-1-phenyl-1,5-dihydro-pyrazol-(4Z)-ylidene]-methyl}-amino)-propionic acid ethyl ester
Synonyms:
CAS NO:132375-23-6
Molecular Formula:
Molecular Weight: 326.355
EINECS: N/A
Product Categories: N/A
Mol File: 132375-23-6.mol
Article Data: 1

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: 2-({Cyano-[3-methyl-5-oxo-1-phenyl-1,5-dihydro-pyrazol-(4Z)-ylidene]-methyl}-amino)-propionic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-({Cyano-[3-methyl-5-oxo-1-phenyl-1,5-dihydro-pyrazol-(4Z)-ylidene]-methyl}-amino)-propionic acid ethyl ester(132375-23-6)
EPA Substance Registry System: 2-({Cyano-[3-methyl-5-oxo-1-phenyl-1,5-dihydro-pyrazol-(4Z)-ylidene]-methyl}-amino)-propionic acid ethyl ester(132375-23-6)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
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RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 132375-23-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 132375-23-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,3,7 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 132375-23:
(8*1)+(7*3)+(6*2)+(5*3)+(4*7)+(3*5)+(2*2)+(1*3)=106
106 % 10 = 6
So 132375-23-6 is a valid CAS Registry Number.

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132375-23-6Relevant articles and documents

Azomethine Yldies from the Reaction of 4-(Dicyanomethylene)-3-methyl-1-phenyl-2-pyrazoline-5-one with α-Amino Acids and Their Esters

Metwally, Saoud A. M.,Aly, Moustafa F.,Abd-Alla, Mohamed A.,Atta, Ferial M.,Abd-El-Monem, Maisa E.

, p. 387 - 389 (2007/10/02)

4-(Dicyanomethylene)-3-methyl-1-phenyl-2-pyrazoline-5-one (1) readily reacts with α-amino acids and their esters by Michael addition and subsequent elimination of HCN to the adducts 2a-k.One of these, 2i (obtained from methyl glycinate), adds stereoselect

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