Cas 1070901-49-3,(E)-N-(4-acetylphenyl)-N-(2-(cyclopentylamino)-1-(2-nitrophenyl)-2-oxoethyl)-4-oxo-4-p-tolylbut-2-enamide

1070901-49-3

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Basic information

Product Name: (E)-N-(4-acetylphenyl)-N-(2-(cyclopentylamino)-1-(2-nitrophenyl)-2-oxoethyl)-4-oxo-4-p-tolylbut-2-enamide
Synonyms: (E)-N-(4-acetylphenyl)-N-(2-(cyclopentylamino)-1-(2-nitrophenyl)-2-oxoethyl)-4-oxo-4-p-tolylbut-2-enamide
CAS NO:1070901-49-3
Molecular Formula:
Molecular Weight: 553.615
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: (E)-N-(4-acetylphenyl)-N-(2-(cyclopentylamino)-1-(2-nitrophenyl)-2-oxoethyl)-4-oxo-4-p-tolylbut-2-enamide(CAS DataBase Reference)
NIST Chemistry Reference: (E)-N-(4-acetylphenyl)-N-(2-(cyclopentylamino)-1-(2-nitrophenyl)-2-oxoethyl)-4-oxo-4-p-tolylbut-2-enamide(1070901-49-3)
EPA Substance Registry System: (E)-N-(4-acetylphenyl)-N-(2-(cyclopentylamino)-1-(2-nitrophenyl)-2-oxoethyl)-4-oxo-4-p-tolylbut-2-enamide(1070901-49-3)

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: 1070901-49-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1070901-49-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,0,9,0 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1070901-49:
(9*1)+(8*0)+(7*7)+(6*0)+(5*9)+(4*0)+(3*1)+(2*4)+(1*9)=123
123 % 10 = 3
So 1070901-49-3 is a valid CAS Registry Number.

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1070901-49-3Relevant academic research and scientific papers

A tandem one-pot, microwave-assisted synthesis of regiochemically differentiated 1,2,4,5-tetrahydro-1,4-benzodiazepin-3-ones

De Silva, Ravindra A.,Santra, Soumava,Andreana, Peter R.

supporting information; experimental part, p. 4541 - 4544 (2009/05/30)

(Chemical Equation Presented) A one-pot, two-step synthesis of the title compounds employs a multicomponent Ugl condensation reaction, microwave irradiation, and Fe(0) as a reductant. Two pathways are accessible; both routes utilize bifunctional, o-nitro-substituted arenes leading to either C2, N4, C5 substitution (A) or C2, N4 substitution (B).

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