Cas 1315610-14-0,ethyl 2-{1-[2-nitro-4-(trifluoromethyl)phenyl]-1H-imidazol-2-yl}-2-oxoacetate

1315610-14-0

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Basic information

Product Name: ethyl 2-{1-[2-nitro-4-(trifluoromethyl)phenyl]-1H-imidazol-2-yl}-2-oxoacetate
Synonyms: ethyl 2-{1-[2-nitro-4-(trifluoromethyl)phenyl]-1H-imidazol-2-yl}-2-oxoacetate
CAS NO:1315610-14-0
Molecular Formula:
Molecular Weight: 357.246
EINECS: N/A
Product Categories: N/A
Mol File: 1315610-14-0.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: ethyl 2-{1-[2-nitro-4-(trifluoromethyl)phenyl]-1H-imidazol-2-yl}-2-oxoacetate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 2-{1-[2-nitro-4-(trifluoromethyl)phenyl]-1H-imidazol-2-yl}-2-oxoacetate(1315610-14-0)
EPA Substance Registry System: ethyl 2-{1-[2-nitro-4-(trifluoromethyl)phenyl]-1H-imidazol-2-yl}-2-oxoacetate(1315610-14-0)

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: 1315610-14-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1315610-14-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,5,6,1 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1315610-14:
(9*1)+(8*3)+(7*1)+(6*5)+(5*6)+(4*1)+(3*0)+(2*1)+(1*4)=110
110 % 10 = 0
So 1315610-14-0 is a valid CAS Registry Number.

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1315610-14-0Relevant articles and documents

Facile synthesis of 2-(2-ethoxy-1,2-dioxoethyl)azoles

Geraschenko, Oleksandr V.,Khodakovskiy, Pavel V.,Shishkin, Oleg V.,Mykhailiuk, Pavel K.,Zaporozhets, Olga A.,Tolmachev, Andrey A.

, p. 1633 - 1637 (2011)

C-Acylation of N-substituted imidazoles with ethyl oxalyl chloride in the presence of N,N-diisopropylethylamine as a base afforded 2-(2-ethoxy-1,2- dioxoethyl)imidazoles in 83-95% yield. Application of this synthetic protocol to thiazoles and triazoles le

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