Cas 1256553-95-3,1-(furan-2-yl)-2-(isobutylamino)-2-oxoethyl 3-{3-(benzylamino)imidazo[1,2-a]pyrimidin-2-yl}benzoate

1256553-95-3

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Basic information

Product Name: 1-(furan-2-yl)-2-(isobutylamino)-2-oxoethyl 3-{3-(benzylamino)imidazo[1,2-a]pyrimidin-2-yl}benzoate
Synonyms:
CAS NO:1256553-95-3
Molecular Formula:
Molecular Weight: 523.591
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: 1-(furan-2-yl)-2-(isobutylamino)-2-oxoethyl 3-{3-(benzylamino)imidazo[1,2-a]pyrimidin-2-yl}benzoate(CAS DataBase Reference)
NIST Chemistry Reference: 1-(furan-2-yl)-2-(isobutylamino)-2-oxoethyl 3-{3-(benzylamino)imidazo[1,2-a]pyrimidin-2-yl}benzoate(1256553-95-3)
EPA Substance Registry System: 1-(furan-2-yl)-2-(isobutylamino)-2-oxoethyl 3-{3-(benzylamino)imidazo[1,2-a]pyrimidin-2-yl}benzoate(1256553-95-3)

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: 1256553-95-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1256553-95-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,6,5,5 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1256553-95:
(9*1)+(8*2)+(7*5)+(6*6)+(5*5)+(4*5)+(3*3)+(2*9)+(1*5)=173
173 % 10 = 3
So 1256553-95-3 is a valid CAS Registry Number.

1256553-95-3Upstream product

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1256553-95-3Relevant academic research and scientific papers

Rapid assembly of polyfunctional structures using a one-pot five- and six-component sequential Groebke-Blackburn/Ugi/Passerini process

Al-Tel, Taleb H.,Al-Qawasmeh, Raed A.,Voelter, Wolfgang

experimental part, p. 5586 - 5593 (2011/02/22)

Sequential addition of up to six components under well-defined conditions results in the formation of novel structures with amino acid, peptide, and heterocyclic components. This process forms up to eight new bonds under very mild conditions and tolerates

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