Cas 656801-24-0,Alaninamide, 3-(4-chloro-3-pyridinyl)-N-[(1,1-dimethylethoxy)carbonyl]-L-alanyl-L-prolyl -2-methyl-N-[(1S)-1-phenylethyl]-

656801-24-0

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Basic information

Product Name: Alaninamide, 3-(4-chloro-3-pyridinyl)-N-[(1,1-dimethylethoxy)carbonyl]-L-alanyl-L-prolyl -2-methyl-N-[(1S)-1-phenylethyl]-
Synonyms:
CAS NO:656801-24-0
Molecular Formula: C30H40ClN5O5
Molecular Weight: 586.131
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: Alaninamide, 3-(4-chloro-3-pyridinyl)-N-[(1,1-dimethylethoxy)carbonyl]-L-alanyl-L-prolyl -2-methyl-N-[(1S)-1-phenylethyl]-(CAS DataBase Reference)
NIST Chemistry Reference: Alaninamide, 3-(4-chloro-3-pyridinyl)-N-[(1,1-dimethylethoxy)carbonyl]-L-alanyl-L-prolyl -2-methyl-N-[(1S)-1-phenylethyl]-(656801-24-0)
EPA Substance Registry System: Alaninamide, 3-(4-chloro-3-pyridinyl)-N-[(1,1-dimethylethoxy)carbonyl]-L-alanyl-L-prolyl -2-methyl-N-[(1S)-1-phenylethyl]-(656801-24-0)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 656801-24-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 656801-24-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,6,8,0 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 656801-24:
(8*6)+(7*5)+(6*6)+(5*8)+(4*0)+(3*1)+(2*2)+(1*4)=170
170 % 10 = 0
So 656801-24-0 is a valid CAS Registry Number.

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656801-24-0Relevant academic research and scientific papers

Preparation of enantiomerically pure pyridyl amino acids from serine.

Tabanella, Stefania,Valancogne, Ingrid,Jackson, Richard F W

, p. 4254 - 4261 (2003)

A range of substituted pyridyl amino acids have been prepared by palladium catalysed cross-coupling of serine-derived organozinc reagents with differently substituted halopyridines. Following this procedure a DMAP analogue has been synthesised and used as

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