Cas 357265-09-9,(S)-2-[(S)-2-Amino-4-((S)-1-ethoxycarbonyl-2-phenyl-ethylcarbamoyl)-butyrylamino]-3-phenyl-propionic acid ethyl ester

357265-09-9

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Basic information

Product Name: (S)-2-[(S)-2-Amino-4-((S)-1-ethoxycarbonyl-2-phenyl-ethylcarbamoyl)-butyrylamino]-3-phenyl-propionic acid ethyl ester
Synonyms: (S)-2-[(S)-2-Amino-4-((S)-1-ethoxycarbonyl-2-phenyl-ethylcarbamoyl)-butyrylamino]-3-phenyl-propionic acid ethyl ester
CAS NO:357265-09-9
Molecular Formula:
Molecular Weight: 497.591
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: (S)-2-[(S)-2-Amino-4-((S)-1-ethoxycarbonyl-2-phenyl-ethylcarbamoyl)-butyrylamino]-3-phenyl-propionic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-[(S)-2-Amino-4-((S)-1-ethoxycarbonyl-2-phenyl-ethylcarbamoyl)-butyrylamino]-3-phenyl-propionic acid ethyl ester(357265-09-9)
EPA Substance Registry System: (S)-2-[(S)-2-Amino-4-((S)-1-ethoxycarbonyl-2-phenyl-ethylcarbamoyl)-butyrylamino]-3-phenyl-propionic acid ethyl ester(357265-09-9)

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: 357265-09-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 357265-09-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,7,2,6 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 357265-09:
(8*3)+(7*5)+(6*7)+(5*2)+(4*6)+(3*5)+(2*0)+(1*9)=159
159 % 10 = 9
So 357265-09-9 is a valid CAS Registry Number.

357265-09-9Upstream product

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357265-09-9Relevant academic research and scientific papers

The synthesis of immobilised chiral dendrimers

Mathews,Beezer,Snowden,Hardy,Mitchell

, p. 807 - 818 (2001)

A one pot synthetic approach to amino acid based chiral dendrimers was shown to give good yields for dendrimers with peptide linkages. Using this synthetic strategy, modification of the peripheral functionality is possible, as is the substitution of other

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