Cas 1448424-56-3,(S)-3-(2-(p-tolyl)-1H-indol-3-yl)-2-(2,2,2-trifluoroacetamido)propanoic acid

1448424-56-3

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Basic information

Product Name: (S)-3-(2-(p-tolyl)-1H-indol-3-yl)-2-(2,2,2-trifluoroacetamido)propanoic acid
Synonyms: (S)-3-(2-(p-tolyl)-1H-indol-3-yl)-2-(2,2,2-trifluoroacetamido)propanoic acid
CAS NO:1448424-56-3
Molecular Formula:
Molecular Weight: 390.362
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)-3-(2-(p-tolyl)-1H-indol-3-yl)-2-(2,2,2-trifluoroacetamido)propanoic acid(CAS DataBase Reference)
NIST Chemistry Reference: (S)-3-(2-(p-tolyl)-1H-indol-3-yl)-2-(2,2,2-trifluoroacetamido)propanoic acid(1448424-56-3)
EPA Substance Registry System: (S)-3-(2-(p-tolyl)-1H-indol-3-yl)-2-(2,2,2-trifluoroacetamido)propanoic acid(1448424-56-3)

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: 1448424-56-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1448424-56-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,8,4,2 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1448424-56:
(9*1)+(8*4)+(7*4)+(6*8)+(5*4)+(4*2)+(3*4)+(2*5)+(1*6)=173
173 % 10 = 3
So 1448424-56-3 is a valid CAS Registry Number.

1448424-56-3Upstream product

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1448424-56-3Relevant academic research and scientific papers

Synthesis of C-2 arylated tryptophan amino acids and related compounds through palladium-catalyzed C-H Activation

Preciado, Sara,Mendive-Tapia, Lorena,Albericio, Fernando,Lavilla, Rodolfo

, p. 8129 - 8135 (2013/09/12)

Tryptophan (Trp) and tryptophan derivatives are C2-arylated. A C-H activation process allows the preparation of both protected and unprotected arylated-Trp amino acids, directly from the amino acid precursor and aryl iodides. The obtained compounds are suitable for standard solid-phase peptide synthesis.

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