Cas 376364-29-3,2-[3-(2-amino-1-methyl-ethyl)-2-(3,5-dimethyl-phenyl)-1<i>H</i>-indol-5-yl]-2-methyl-propionic acid ethyl ester

376364-29-3

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Basic information

Product Name: 2-[3-(2-amino-1-methyl-ethyl)-2-(3,5-dimethyl-phenyl)-1H-indol-5-yl]-2-methyl-propionic acid ethyl ester
Synonyms:
CAS NO:376364-29-3
Molecular Formula:
Molecular Weight: 392.541
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-[3-(2-amino-1-methyl-ethyl)-2-(3,5-dimethyl-phenyl)-1H-indol-5-yl]-2-methyl-propionic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-[3-(2-amino-1-methyl-ethyl)-2-(3,5-dimethyl-phenyl)-1H-indol-5-yl]-2-methyl-propionic acid ethyl ester(376364-29-3)
EPA Substance Registry System: 2-[3-(2-amino-1-methyl-ethyl)-2-(3,5-dimethyl-phenyl)-1H-indol-5-yl]-2-methyl-propionic acid ethyl ester(376364-29-3)

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: 376364-29-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 376364-29-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,6,3,6 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 376364-29:
(8*3)+(7*7)+(6*6)+(5*3)+(4*6)+(3*4)+(2*2)+(1*9)=173
173 % 10 = 3
So 376364-29-3 is a valid CAS Registry Number.

376364-29-3Upstream product

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376364-29-3Relevant academic research and scientific papers

Synthesis of chiral β-methyl tryptamine-derived GnRH antagonists

Simeone, Joseph P.,Bugianesi, Robert L.,Ponpipom, Mitree M.,Goulet, Mark T.,Levorse, Mark S.,Desai, Ranjit C.

, p. 6459 - 6461 (2007/10/03)

The stereospecific formation of 2-aryl-β-methyl tryptamine derivatives 15 and 16 from chiral 4-chloro-1-(3,5-dimethylphenyl)-3-methylbutanones is described. These intermediates were further manipulated into the GnRH antagonists 1b and 1c in five steps.

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