Cas 865094-47-9,Carbamic acid, [3-(1,1-dimethylethyl)-1-(4-methylphenyl)-1H-pyrazol-5-yl]-, 1-methylethenyl ester

865094-47-9

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Basic information

Product Name: Carbamic acid, [3-(1,1-dimethylethyl)-1-(4-methylphenyl)-1H-pyrazol-5-yl]-, 1-methylethenyl ester
Synonyms:
CAS NO:865094-47-9
Molecular Formula: C18H23N3O2
Molecular Weight: 313.4
EINECS: N/A
Product Categories: N/A
Mol File: 865094-47-9.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: Carbamic acid, [3-(1,1-dimethylethyl)-1-(4-methylphenyl)-1H-pyrazol-5-yl]-, 1-methylethenyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Carbamic acid, [3-(1,1-dimethylethyl)-1-(4-methylphenyl)-1H-pyrazol-5-yl]-, 1-methylethenyl ester(865094-47-9)
EPA Substance Registry System: Carbamic acid, [3-(1,1-dimethylethyl)-1-(4-methylphenyl)-1H-pyrazol-5-yl]-, 1-methylethenyl ester(865094-47-9)

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: 865094-47-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 865094-47-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,5,0,9 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 865094-47:
(8*8)+(7*6)+(6*5)+(5*0)+(4*9)+(3*4)+(2*4)+(1*7)=199
199 % 10 = 9
So 865094-47-9 is a valid CAS Registry Number.

865094-47-9Upstream product

865094-47-9Downstream Products

865094-47-9Relevant articles and documents

Practical synthesis of unsymmetrical ureas from isopropenyl carbamates

Gallou, Isabelle,Eriksson, Magnus,Zeng, Xingzhong,Senanayake, Chris,Farina, Vittorio

, p. 6960 - 6963 (2007/10/03)

A very convenient method for the synthesis of unsymmetrical ureas is described, based on isopropenyl carbamates. The synthetic efficiency of traditional methods for urea formation, such as use of phosgene or alkyl and aryl carbamates, is limited by the fo

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