Cas 446274-56-2,N-2,2-dimethoxyethyl α,β-dehydro-N-[N-(trifluoroacetyl)-1-phenylalanyl]-methylalaninamide

446274-56-2

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Basic information

Product Name: N-2,2-dimethoxyethyl α,β-dehydro-N-[N-(trifluoroacetyl)-1-phenylalanyl]-methylalaninamide
Synonyms: N-2,2-dimethoxyethyl α,β-dehydro-N-[N-(trifluoroacetyl)-1-phenylalanyl]-methylalaninamide
CAS NO:446274-56-2
Molecular Formula:
Molecular Weight: 431.412
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-2,2-dimethoxyethyl α,β-dehydro-N-[N-(trifluoroacetyl)-1-phenylalanyl]-methylalaninamide(CAS DataBase Reference)
NIST Chemistry Reference: N-2,2-dimethoxyethyl α,β-dehydro-N-[N-(trifluoroacetyl)-1-phenylalanyl]-methylalaninamide(446274-56-2)
EPA Substance Registry System: N-2,2-dimethoxyethyl α,β-dehydro-N-[N-(trifluoroacetyl)-1-phenylalanyl]-methylalaninamide(446274-56-2)

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: 446274-56-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 446274-56-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,6,2,7 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 446274-56:
(8*4)+(7*4)+(6*6)+(5*2)+(4*7)+(3*4)+(2*5)+(1*6)=162
162 % 10 = 2
So 446274-56-2 is a valid CAS Registry Number.

446274-56-2Upstream product

22483-09-6 2,2-dimethoxyethylamine

446274-56-2Downstream Products

446274-56-2Relevant academic research and scientific papers

A biomimetic synthesis of coelenterazine analogs

Devillers, Ingrid,Arrault, Axelle,Olive, Gilles,Marchand-Brynaert, Jacqueline

, p. 3161 - 3164 (2002)

N-(Trifluoroacetyl)dehydrodipeptides 2-3 were coupled to aminomethylene dimethylacetal derivatives 4-5. The resulting pseudo-tripeptides 6 were stepwise deprotected (carbonyl function (7) then amine function) and in situ cyclized into imidazolopyrazines 1.

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