Cas 147151-62-0,2-Propenoic acid,3-[4-[bis(2-chloroethyl)amino]phenyl]-,(4aS,4bR,6aS,8R,10aS,10bS,12aS)-octadecahydro-10a,12a-dimethyl-2-oxonaphtho[2,1-f]quinolin-8-ylester

147151-62-0

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Product Name: 2-Propenoic acid,3-[4-[bis(2-chloroethyl)amino]phenyl]-,(4aS,4bR,6aS,8R,10aS,10bS,12aS)-octadecahydro-10a,12a-dimethyl-2-oxonaphtho[2,1-f]quinolin-8-ylester
Synonyms: 17a-Aza-D-homoandrostan-17-one,3-[[3-[4-[bis(2-chloroethyl)amino]phenyl]-1-oxo-2-propenyl]oxy]-, (3a,5a)-
CAS NO:147151-62-0
Molecular Formula: C32H44 Cl2 N2 O3
Molecular Weight: 575.619
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: 2-Propenoic acid,3-[4-[bis(2-chloroethyl)amino]phenyl]-,(4aS,4bR,6aS,8R,10aS,10bS,12aS)-octadecahydro-10a,12a-dimethyl-2-oxonaphtho[2,1-f]quinolin-8-ylester(CAS DataBase Reference)
NIST Chemistry Reference: 2-Propenoic acid,3-[4-[bis(2-chloroethyl)amino]phenyl]-,(4aS,4bR,6aS,8R,10aS,10bS,12aS)-octadecahydro-10a,12a-dimethyl-2-oxonaphtho[2,1-f]quinolin-8-ylester(147151-62-0)
EPA Substance Registry System: 2-Propenoic acid,3-[4-[bis(2-chloroethyl)amino]phenyl]-,(4aS,4bR,6aS,8R,10aS,10bS,12aS)-octadecahydro-10a,12a-dimethyl-2-oxonaphtho[2,1-f]quinolin-8-ylester(147151-62-0)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
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RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 147151-62-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 147151-62-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,1,5 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 147151-62:
(8*1)+(7*4)+(6*7)+(5*1)+(4*5)+(3*1)+(2*6)+(1*2)=120
120 % 10 = 0
So 147151-62-0 is a valid CAS Registry Number.

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147151-62-0Relevant academic research and scientific papers

Structure-anticancer and structure-genetic activity relationships of homo- aza-steroidal esters of N,N-bis(2-chloroethyl)aminocinnamic acid isomers

Catsoulacos,Camoutsis,Papageorgiou,Margariti,Psaraki,Demopoulos

, p. 204 - 208 (1993)

Four steroidal lactams of the A- and D-rings were used for the esterification in the C-3 or C-17 positions, respectively, of their nuclei with the N,N-bis(2-chloroethyl)aminocinnamic acid isomers. The condensation reaction of the hydroxylic group of the s

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