Cas 163333-46-8,1,2-Distearoyl-3-{(S)-N-tert-butoxycarbonyl-4-[bis(2-chloroethyl)amino]phenylalanyl}glycerol

163333-46-8

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Basic information

Product Name: 1,2-Distearoyl-3-{(S)-N-tert-butoxycarbonyl-4-[bis(2-chloroethyl)amino]phenylalanyl}glycerol
Synonyms: 1,2-Distearoyl-3-{(S)-N-tert-butoxycarbonyl-4-[bis(2-chloroethyl)amino]phenylalanyl}glycerol
CAS NO:163333-46-8
Molecular Formula:
Molecular Weight: 1012.34
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: 1,2-Distearoyl-3-{(S)-N-tert-butoxycarbonyl-4-[bis(2-chloroethyl)amino]phenylalanyl}glycerol(CAS DataBase Reference)
NIST Chemistry Reference: 1,2-Distearoyl-3-{(S)-N-tert-butoxycarbonyl-4-[bis(2-chloroethyl)amino]phenylalanyl}glycerol(163333-46-8)
EPA Substance Registry System: 1,2-Distearoyl-3-{(S)-N-tert-butoxycarbonyl-4-[bis(2-chloroethyl)amino]phenylalanyl}glycerol(163333-46-8)

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: 163333-46-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 163333-46-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,3,3 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 163333-46:
(8*1)+(7*6)+(6*3)+(5*3)+(4*3)+(3*3)+(2*4)+(1*6)=118
118 % 10 = 8
So 163333-46-8 is a valid CAS Registry Number.

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163333-46-8Relevant academic research and scientific papers

The synthesis of novel melphalan derivatives as potential antineoplastic agents

Morris,Atassi,Guilbaud,Cordi

, p. 343 - 349 (1997)

Five derivatives of melphalan (S)-4-[bis(2-chloroethyl)amino]phenylalanine), an alkylating agent presently employed as an antieoplastic in humans, were designed and synthesised as potential prodrugs. Their antitumour activity was tested against P388 leuka

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