Cas 1448522-31-3,N-(trifluoroacetyl)-(S)-phenylalanyl-(R)-[2-(tributylstannyl)allyl]glycine 3,4-dihydroquinolinide

1448522-31-3

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Basic information

Product Name: N-(trifluoroacetyl)-(S)-phenylalanyl-(R)-[2-(tributylstannyl)allyl]glycine 3,4-dihydroquinolinide
Synonyms:
CAS NO:1448522-31-3
Molecular Formula:
Molecular Weight: 762.543
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: N-(trifluoroacetyl)-(S)-phenylalanyl-(R)-[2-(tributylstannyl)allyl]glycine 3,4-dihydroquinolinide(CAS DataBase Reference)
NIST Chemistry Reference: N-(trifluoroacetyl)-(S)-phenylalanyl-(R)-[2-(tributylstannyl)allyl]glycine 3,4-dihydroquinolinide(1448522-31-3)
EPA Substance Registry System: N-(trifluoroacetyl)-(S)-phenylalanyl-(R)-[2-(tributylstannyl)allyl]glycine 3,4-dihydroquinolinide(1448522-31-3)

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: 1448522-31-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1448522-31-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,8,5,2 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1448522-31:
(9*1)+(8*4)+(7*4)+(6*8)+(5*5)+(4*2)+(3*2)+(2*3)+(1*1)=163
163 % 10 = 3
So 1448522-31-3 is a valid CAS Registry Number.

1448522-31-3Upstream product

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1448522-31-3Relevant academic research and scientific papers

Palladium-catalyzed allylic alkylations as versatile tool for amino acid and peptide modifications

Kazmaier, Uli,Bayer, Anton,Deska, Jan

, p. 1463 - 1468 (2013)

Palladium-catalyzed allylic alkylations are especially suitable for the introduction of γ,δ-unsaturated side chains into amino acids and even peptides. Glycine ester enolates are generally used as nucleophiles in these reactions, they react at a very low

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