Cas 130677-10-0,(2S,3R)-4-bromobenzyl 5-(4,5-bismethoxycarbonyl-1,2,3-triazol-1-yl)-3-hydroxy-2-(2-oxoazetidin-1-yl)valerate

130677-10-0

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Basic information

Product Name: (2S,3R)-4-bromobenzyl 5-(4,5-bismethoxycarbonyl-1,2,3-triazol-1-yl)-3-hydroxy-2-(2-oxoazetidin-1-yl)valerate
Synonyms:
CAS NO:130677-10-0
Molecular Formula:
Molecular Weight: 539.34
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: (2S,3R)-4-bromobenzyl 5-(4,5-bismethoxycarbonyl-1,2,3-triazol-1-yl)-3-hydroxy-2-(2-oxoazetidin-1-yl)valerate(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3R)-4-bromobenzyl 5-(4,5-bismethoxycarbonyl-1,2,3-triazol-1-yl)-3-hydroxy-2-(2-oxoazetidin-1-yl)valerate(130677-10-0)
EPA Substance Registry System: (2S,3R)-4-bromobenzyl 5-(4,5-bismethoxycarbonyl-1,2,3-triazol-1-yl)-3-hydroxy-2-(2-oxoazetidin-1-yl)valerate(130677-10-0)

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: 130677-10-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 130677-10-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,6,7 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 130677-10:
(8*1)+(7*3)+(6*0)+(5*6)+(4*7)+(3*7)+(2*1)+(1*0)=110
110 % 10 = 0
So 130677-10-0 is a valid CAS Registry Number.

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130677-10-0Relevant academic research and scientific papers

Studies on the Biosynthesis of Clavulanic Acid. Part 4. Synthetic Routes to the Monocyclic β-Lactam Precursor, Proclavaminic Acid

Baggaley, Keith H.,Elson, Stephen W.,Nicholson, Neville H.,Sime, John T.

, p. 1513 - 1520 (2007/10/02)

Aldol condensation of 3-substituted propionaldehydes with the lithium enolate of ethyl or benzyl(2-oxoazetidin-1-yl)acetate yielded derivatives of proclavaminic acid.The proportion of the threo diastereoisomer in the aldol product could be increased by th

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