Cas 700358-67-4,5-(1-phenyl-ethylcarbamoyl)-2-<i>p</i>-tolyl-3,4-dihydro-2<i>H</i>-pyrazole-3-carboxylic acid ethyl ester

700358-67-4

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Basic information

Product Name: 5-(1-phenyl-ethylcarbamoyl)-2-p-tolyl-3,4-dihydro-2H-pyrazole-3-carboxylic acid ethyl ester
Synonyms:
CAS NO:700358-67-4
Molecular Formula:
Molecular Weight: 379.459
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: 5-(1-phenyl-ethylcarbamoyl)-2-p-tolyl-3,4-dihydro-2H-pyrazole-3-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 5-(1-phenyl-ethylcarbamoyl)-2-p-tolyl-3,4-dihydro-2H-pyrazole-3-carboxylic acid ethyl ester(700358-67-4)
EPA Substance Registry System: 5-(1-phenyl-ethylcarbamoyl)-2-p-tolyl-3,4-dihydro-2H-pyrazole-3-carboxylic acid ethyl ester(700358-67-4)

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: 700358-67-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 700358-67-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,0,3,5 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 700358-67:
(8*7)+(7*0)+(6*0)+(5*3)+(4*5)+(3*8)+(2*6)+(1*7)=134
134 % 10 = 4
So 700358-67-4 is a valid CAS Registry Number.

700358-67-4Upstream product

140-88-5 ethyl acrylate

700358-67-4Downstream Products

700358-67-4Relevant academic research and scientific papers

The first case of diastereoselective cycloadditions of enantiopure nitrilimines in aqueous media

Molteni, Giorgio

, p. 1077 - 1079 (2004)

The diastereoselective cycloadditions of enantiopure nitrilimines 4 with ethyl acrylate were exploited in dry toluene and in aqueous sodium hydrogencarbonate as reaction media. Shorter reaction times and improved diastereoisomeric ratios of the resulting 5-ethoxycarbonyl-4,5-dihydropyrazoles 5 and 6 were observed in aqueous media.

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