Cas 557764-48-4,{2-[2-(9<i>H</i>-fluoren-9-ylmethoxycarbonylamino)-3-(1<i>H</i>-indol-3-yl)-propionylamino]-benzoylamino}-acetic acid methyl ester

557764-48-4

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Basic information

Product Name: {2-[2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(1H-indol-3-yl)-propionylamino]-benzoylamino}-acetic acid methyl ester
Synonyms: {2-[2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(1H-indol-3-yl)-propionylamino]-benzoylamino}-acetic acid methyl ester
CAS NO:557764-48-4
Molecular Formula:
Molecular Weight: 616.673
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: {2-[2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(1H-indol-3-yl)-propionylamino]-benzoylamino}-acetic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: {2-[2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(1H-indol-3-yl)-propionylamino]-benzoylamino}-acetic acid methyl ester(557764-48-4)
EPA Substance Registry System: {2-[2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(1H-indol-3-yl)-propionylamino]-benzoylamino}-acetic acid methyl ester(557764-48-4)

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: 557764-48-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 557764-48-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,7,7,6 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 557764-48:
(8*5)+(7*5)+(6*7)+(5*7)+(4*6)+(3*4)+(2*4)+(1*8)=204
204 % 10 = 4
So 557764-48-4 is a valid CAS Registry Number.

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557764-48-4Relevant academic research and scientific papers

A short synthesis of de-'prenyl'-ardeemin

Hernández, Fernando,Avenda?o, Carmen,S?llhuber, Mónica

, p. 3367 - 3369 (2003)

A four-step synthesis of the ardeemin framework by starting from N-2-aminobenzoyl-α-amino esters is described. In the last step, the acid promoted cyclization of the 1,4-anti-4-alkyl-1-(3-indolylmethyl)-2,4-dihydro-1H-pyrazino[2,1-b] quinazoline-3,6-diones occurs irreversible and stereocontrolled.

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