Cas 444154-80-7,N,N-[(2S,3R)-2-benzyloxycarbonylamino-3-(3,4-dibenzyloxyphenyl)-3-hydroxypropionyl]-β-alanyl-β-alanine methyl ester

444154-80-7

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Basic information

Product Name: N,N-[(2S,3R)-2-benzyloxycarbonylamino-3-(3,4-dibenzyloxyphenyl)-3-hydroxypropionyl]-β-alanyl-β-alanine methyl ester
Synonyms: N,N-[(2S,3R)-2-benzyloxycarbonylamino-3-(3,4-dibenzyloxyphenyl)-3-hydroxypropionyl]-β-alanyl-β-alanine methyl ester
CAS NO:444154-80-7
Molecular Formula:
Molecular Weight: 683.758
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,N-[(2S,3R)-2-benzyloxycarbonylamino-3-(3,4-dibenzyloxyphenyl)-3-hydroxypropionyl]-β-alanyl-β-alanine methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: N,N-[(2S,3R)-2-benzyloxycarbonylamino-3-(3,4-dibenzyloxyphenyl)-3-hydroxypropionyl]-β-alanyl-β-alanine methyl ester(444154-80-7)
EPA Substance Registry System: N,N-[(2S,3R)-2-benzyloxycarbonylamino-3-(3,4-dibenzyloxyphenyl)-3-hydroxypropionyl]-β-alanyl-β-alanine methyl ester(444154-80-7)

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: 444154-80-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 444154-80-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,4,1,5 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 444154-80:
(8*4)+(7*4)+(6*4)+(5*1)+(4*5)+(3*4)+(2*8)+(1*0)=137
137 % 10 = 7
So 444154-80-7 is a valid CAS Registry Number.

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444154-80-7Relevant academic research and scientific papers

Total synthesis of exochelin MN and analogues.

Dong,Miller, Marvin J

, p. 4759 - 4770 (2007/10/03)

The first total synthesis of exochelin MN is described along with rationally designed analogues. The required L-threo-beta-hydroxyamino acid components were constructed using either Sharpless asymmetric aminohydroxylation reactions or an aldol reaction of imidazolidinone 19. A new concise procedure for the preparation of the constituent six-membered cyclic hydroxamate was developed. In addition, a plausible mechanism for exochelin MN-mediated iron(III) transport was proposed. Biological studies of these compounds will be used to evaluate this hypothesis.

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