Cas 448963-30-2,benzyl ((S)-1-(((S)-1-((4-(hydroxymethyl)phenyl)amino)-1-oxo-5-ureidopentan-2-yl)amino)-4-methyl-1-oxopentan-2-yl)carbamate

448963-30-2

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Basic information

Product Name: benzyl ((S)-1-(((S)-1-((4-(hydroxymethyl)phenyl)amino)-1-oxo-5-ureidopentan-2-yl)amino)-4-methyl-1-oxopentan-2-yl)carbamate
Synonyms: benzyl ((S)-1-(((S)-1-((4-(hydroxymethyl)phenyl)amino)-1-oxo-5-ureidopentan-2-yl)amino)-4-methyl-1-oxopentan-2-yl)carbamate
CAS NO:448963-30-2
Molecular Formula:
Molecular Weight: 527.621
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: benzyl ((S)-1-(((S)-1-((4-(hydroxymethyl)phenyl)amino)-1-oxo-5-ureidopentan-2-yl)amino)-4-methyl-1-oxopentan-2-yl)carbamate(CAS DataBase Reference)
NIST Chemistry Reference: benzyl ((S)-1-(((S)-1-((4-(hydroxymethyl)phenyl)amino)-1-oxo-5-ureidopentan-2-yl)amino)-4-methyl-1-oxopentan-2-yl)carbamate(448963-30-2)
EPA Substance Registry System: benzyl ((S)-1-(((S)-1-((4-(hydroxymethyl)phenyl)amino)-1-oxo-5-ureidopentan-2-yl)amino)-4-methyl-1-oxopentan-2-yl)carbamate(448963-30-2)

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: 448963-30-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 448963-30-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,8,9,6 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 448963-30:
(8*4)+(7*4)+(6*8)+(5*9)+(4*6)+(3*3)+(2*3)+(1*0)=192
192 % 10 = 2
So 448963-30-2 is a valid CAS Registry Number.

448963-30-2Upstream product

448963-30-2Downstream Products

448963-37-9 Carbonic acid 4-[(S)-2-((S)-2-benzyloxycarbonylamino-4-methyl-pentanoylamino)-5-ureido-pentanoylamino]-benzyl ester 4-nitro-phenyl ester

448963-30-2Relevant academic research and scientific papers

Cathepsin B-sensitive dipeptide prodrugs. 1. A model study of structural requirements for efficient release of doxorubicin

Dubowchik, Gene M.,Firestone, Raymond A.

, p. 3343 - 3346 (2007/10/03)

A series of lysosomal protease-sensitive peptides attached to doxorubicin (DOX) was prepared as model substrates for internalizing anticancer immunoconjugates and potential antimetastasis prodrugs. Rates of cathepsin B-mediated release of free drug was measured for each, and human plasma stabilities for representative examples.

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