Cas 2754-05-4,[(S)-2-((S)-2-benzyloxycarbonylamino-3-phenyl-propionylamino)-3-phenyl-propionylamino]acetic acid ethyl ester

2754-05-4

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Basic information

Product Name: [(S)-2-((S)-2-benzyloxycarbonylamino-3-phenyl-propionylamino)-3-phenyl-propionylamino]acetic acid ethyl ester
Synonyms:
CAS NO:2754-05-4
Molecular Formula:
Molecular Weight: 531.609
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-benzyloxycarbonylamino-3-phenyl-propionylamino)-3-phenyl-propionylamino]acetic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [(S)-2-((S)-2-benzyloxycarbonylamino-3-phenyl-propionylamino)-3-phenyl-propionylamino]acetic acid ethyl ester(2754-05-4)
EPA Substance Registry System: [(S)-2-((S)-2-benzyloxycarbonylamino-3-phenyl-propionylamino)-3-phenyl-propionylamino]acetic acid ethyl ester(2754-05-4)

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: 2754-05-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 2754-05-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,5 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2754-05:
(6*2)+(5*7)+(4*5)+(3*4)+(2*0)+(1*5)=84
84 % 10 = 4
So 2754-05-4 is a valid CAS Registry Number.

2754-05-4Upstream product

2754-05-4Downstream Products

2754-05-4Relevant academic research and scientific papers

Studies on the application of the Passerini reaction and enzymatic procedures to the synthesis of tripeptide mimetics

Szymanski, Wiktor,Zwolinska, Magdalena,Ostaszewski, Ryszard

, p. 7647 - 7653 (2008/02/08)

A new, efficient method for the multicomponent synthesis of tripeptide mimetics is presented. Simple, chemoenzymatic transformations of Passerini reaction products enable the introduction of varied amino acid moieties into the tripeptide scaffold, with co

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