Cas 566180-41-4,L-Phenylalanine, N-[4-[[[(1,1-dimethylethoxy)carbonyl]amino]methyl]benzoyl]-b-alanyl-L-a- aspartyl-, bis(phenylmethyl) ester

566180-41-4

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Basic information

Product Name: L-Phenylalanine, N-[4-[[[(1,1-dimethylethoxy)carbonyl]amino]methyl]benzoyl]-b-alanyl-L-a- aspartyl-, bis(phenylmethyl) ester
Synonyms:
CAS NO:566180-41-4
Molecular Formula: C43H48N4O9
Molecular Weight: 764.876
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: L-Phenylalanine, N-[4-[[[(1,1-dimethylethoxy)carbonyl]amino]methyl]benzoyl]-b-alanyl-L-a- aspartyl-, bis(phenylmethyl) ester(CAS DataBase Reference)
NIST Chemistry Reference: L-Phenylalanine, N-[4-[[[(1,1-dimethylethoxy)carbonyl]amino]methyl]benzoyl]-b-alanyl-L-a- aspartyl-, bis(phenylmethyl) ester(566180-41-4)
EPA Substance Registry System: L-Phenylalanine, N-[4-[[[(1,1-dimethylethoxy)carbonyl]amino]methyl]benzoyl]-b-alanyl-L-a- aspartyl-, bis(phenylmethyl) ester(566180-41-4)

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: 566180-41-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 566180-41-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,6,1,8 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 566180-41:
(8*5)+(7*6)+(6*6)+(5*1)+(4*8)+(3*0)+(2*4)+(1*1)=164
164 % 10 = 4
So 566180-41-4 is a valid CAS Registry Number.

566180-41-4Upstream product

566180-41-4Downstream Products

566180-42-5 Boc-(4-aminomethylbenzoyl)-β-Ala-Asp-Phe-OH

566180-41-4Relevant academic research and scientific papers

Synthesis and comparison of physicochemical, transport, and antithrombic properties of a cyclic prodrug and the parent RGD peptidomimetic

Xu, Christine R.,He, Henry T.,Song, Xiaoping,Siahaan, Teruna J.

, p. 2861 - 2869 (2007/10/03)

Cyclic prodrug 1 was derived from RGD peptidomimetic 2 by linking the amino and carboxylic acid groups via an (acyloxy)alkoxy linker. The formation of a cyclic prodrug can transiently alter the physicochemical properties of the RGD peptidomimetic. Cyclic

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