Cas 1003005-48-8,N-((E)-1-propylpent-1-enyl)(2S)-4-methyl-2-[(phenylmethoxy)carbonylamino]pentanamide

1003005-48-8

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Basic information

Product Name: N-((E)-1-propylpent-1-enyl)(2S)-4-methyl-2-[(phenylmethoxy)carbonylamino]pentanamide
Synonyms: N-((E)-1-propylpent-1-enyl)(2S)-4-methyl-2-[(phenylmethoxy)carbonylamino]pentanamide
CAS NO:1003005-48-8
Molecular Formula:
Molecular Weight: 374.524
EINECS: N/A
Product Categories: N/A
Mol File: 1003005-48-8.mol
Article Data: 1

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-((E)-1-propylpent-1-enyl)(2S)-4-methyl-2-[(phenylmethoxy)carbonylamino]pentanamide(CAS DataBase Reference)
NIST Chemistry Reference: N-((E)-1-propylpent-1-enyl)(2S)-4-methyl-2-[(phenylmethoxy)carbonylamino]pentanamide(1003005-48-8)
EPA Substance Registry System: N-((E)-1-propylpent-1-enyl)(2S)-4-methyl-2-[(phenylmethoxy)carbonylamino]pentanamide(1003005-48-8)

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: 1003005-48-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1003005-48-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,3,0,0 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1003005-48:
(9*1)+(8*0)+(7*0)+(6*3)+(5*0)+(4*0)+(3*5)+(2*4)+(1*8)=58
58 % 10 = 8
So 1003005-48-8 is a valid CAS Registry Number.

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1003005-48-8Relevant articles and documents

Amino acid derived enamides: Synthesis and aminopeptidase activity

Cesati III, Richard R.,Dwyer, Greg,Jones, Reinaldo C.,Hayes, Megan P.,Yalamanchili, Padmaja,Casebier, David S.

, p. 5617 - 5620 (2008/09/18)

Recently developed copper-catalyzed coupling methodology has been applied to the synthesis of amino acid derived enamides. Bond formation proved to be strongly influenced by protection strategy and vinyl iodide substitution while tolerant of limited side chain functionality. Assessment of aminopeptidase activity revealed a preference for (E)-1,2-disubstituted constructs.

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