Cas 1291053-73-0,4-(1-benzyl-3,3-dimethyl-4-oxoazetidin-2-yl)-3-O-benzyl-1,2-O-isopropyliden-β-L-threofuranose

1291053-73-0

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Basic information

Product Name: 4-(1-benzyl-3,3-dimethyl-4-oxoazetidin-2-yl)-3-O-benzyl-1,2-O-isopropyliden-β-L-threofuranose
Synonyms: 4-(1-benzyl-3,3-dimethyl-4-oxoazetidin-2-yl)-3-O-benzyl-1,2-O-isopropyliden-β-L-threofuranose
CAS NO:1291053-73-0
Molecular Formula:
Molecular Weight: 437.536
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: 4-(1-benzyl-3,3-dimethyl-4-oxoazetidin-2-yl)-3-O-benzyl-1,2-O-isopropyliden-β-L-threofuranose(CAS DataBase Reference)
NIST Chemistry Reference: 4-(1-benzyl-3,3-dimethyl-4-oxoazetidin-2-yl)-3-O-benzyl-1,2-O-isopropyliden-β-L-threofuranose(1291053-73-0)
EPA Substance Registry System: 4-(1-benzyl-3,3-dimethyl-4-oxoazetidin-2-yl)-3-O-benzyl-1,2-O-isopropyliden-β-L-threofuranose(1291053-73-0)

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: 1291053-73-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1291053-73-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,1,0,5 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1291053-73:
(9*1)+(8*2)+(7*9)+(6*1)+(5*0)+(4*5)+(3*3)+(2*7)+(1*3)=140
140 % 10 = 0
So 1291053-73-0 is a valid CAS Registry Number.

1291053-73-0Upstream product

1291053-73-0Downstream Products

1291053-92-3 5-benzylamino-3-O-benzyl-5-deoxy-6,6-dimethyl-1,2-O-isopropyliden-α-L-idofuranuronic acid

1291053-73-0Relevant academic research and scientific papers

Highly diastereoselective indium-mediated synthesis of β-lactam carbohydrates from imines

Soengas, Raquel G.,Segade, Yuri,Jiménez, Carlos,Rodríguez, Jaime

experimental part, p. 2617 - 2622 (2011/04/25)

A simple and very effective approach to versatile carbohydrate β-lactam synthons of predictable absolute configuration has been developed. The procedure, which is based on the indium-mediated reaction of imines and bromoesters, was applied to the enantios

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