Cas 1155257-60-5,ethyl 3-(tert-butylamino)-2-(4-chlorophenyl)-5H-imidazo[1,2-b]pyrazole-7-carboxylate

1155257-60-5

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Basic information

Product Name: ethyl 3-(tert-butylamino)-2-(4-chlorophenyl)-5H-imidazo[1,2-b]pyrazole-7-carboxylate
Synonyms: ethyl 3-(tert-butylamino)-2-(4-chlorophenyl)-5H-imidazo[1,2-b]pyrazole-7-carboxylate
CAS NO:1155257-60-5
Molecular Formula:
Molecular Weight: 360.843
EINECS: N/A
Product Categories: N/A
Mol File: 1155257-60-5.mol
Article Data: 2

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 3-(tert-butylamino)-2-(4-chlorophenyl)-5H-imidazo[1,2-b]pyrazole-7-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 3-(tert-butylamino)-2-(4-chlorophenyl)-5H-imidazo[1,2-b]pyrazole-7-carboxylate(1155257-60-5)
EPA Substance Registry System: ethyl 3-(tert-butylamino)-2-(4-chlorophenyl)-5H-imidazo[1,2-b]pyrazole-7-carboxylate(1155257-60-5)

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: 1155257-60-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1155257-60-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,5,2,5 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1155257-60:
(9*1)+(8*1)+(7*5)+(6*5)+(5*2)+(4*5)+(3*7)+(2*6)+(1*0)=145
145 % 10 = 5
So 1155257-60-5 is a valid CAS Registry Number.

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1155257-60-5Relevant articles and documents

A highly flexible and efficient ugi-type multicomponent synthesis of versatile n-fused aminoimidazoles

Guchhait, Sankar K.,Madaan, Chetna,Thakkar, Balmukund S.

experimental part, p. 3293 - 3300 (2010/02/28)

A microwave-promoted highly flexible and efficient Ugi-type multicomponent reaction of heterocyclic amidines with aldehydes and isocyanides catalyzed by zirconium(IV) chloride was developed. The general protocol offered the very reliable synthesis of a li

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