Cas 1126450-30-3,(R)-2-(tert-butoxycarbonyl(methyl)amino)-3-(3-nitrophenyl)propanoic acid

1126450-30-3

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Basic information

Product Name: (R)-2-(tert-butoxycarbonyl(methyl)amino)-3-(3-nitrophenyl)propanoic acid
Synonyms: (R)-2-(tert-butoxycarbonyl(methyl)amino)-3-(3-nitrophenyl)propanoic acid
CAS NO:1126450-30-3
Molecular Formula:
Molecular Weight: 324.334
EINECS: N/A
Product Categories: N/A
Mol File: 1126450-30-3.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: (R)-2-(tert-butoxycarbonyl(methyl)amino)-3-(3-nitrophenyl)propanoic acid(CAS DataBase Reference)
NIST Chemistry Reference: (R)-2-(tert-butoxycarbonyl(methyl)amino)-3-(3-nitrophenyl)propanoic acid(1126450-30-3)
EPA Substance Registry System: (R)-2-(tert-butoxycarbonyl(methyl)amino)-3-(3-nitrophenyl)propanoic acid(1126450-30-3)

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: 1126450-30-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1126450-30-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,6,4,5 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1126450-30:
(9*1)+(8*1)+(7*2)+(6*6)+(5*4)+(4*5)+(3*0)+(2*3)+(1*0)=113
113 % 10 = 3
So 1126450-30-3 is a valid CAS Registry Number.

1126450-30-3Upstream product

1126450-30-3Downstream Products

1126450-32-5 (R)-methyl-2-(tert-butoxycarbonyl(methyl)amino)-3-(3-nitrophenyl)propanoate

1126450-30-3Relevant articles and documents

Synthesis and evaluation of vancomycin aglycon analogues that bear modifications in the N-terminal D-leucyl amino acid

Crane, Christine M.,Boger, Dale L.

supporting information; experimental part, p. 1471 - 1476 (2009/12/26)

The synthesis and biological evaluation of a series of vancomycin aglycon analogues bearing alternative residue 1 N-methyl-d-amino acids are described. The analogues were prepared to define whether H-bonding d-amino acids could improve the affinity for th

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