Cas 547769-47-1,acetic acid (3S,4R,3a'R,5'R,6'S,6a'R)-5'-{1-(4-methoxyphenyl)-4-oxo-3-phenoxyazetidin-2-yl}-2',2'-dimethyl-tetrahydrofuro[2',3'-d][1',3']dioxol-6'-yl ester

547769-47-1

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Basic information

Product Name: acetic acid (3S,4R,3a'R,5'R,6'S,6a'R)-5'-{1-(4-methoxyphenyl)-4-oxo-3-phenoxyazetidin-2-yl}-2',2'-dimethyl-tetrahydrofuro[2',3'-d][1',3']dioxol-6'-yl ester
Synonyms: acetic acid (3S,4R,3a'R,5'R,6'S,6a'R)-5'-{1-(4-methoxyphenyl)-4-oxo-3-phenoxyazetidin-2-yl}-2',2'-dimethyl-tetrahydrofuro[2',3'-d][1',3']dioxol-6'-yl ester
CAS NO:547769-47-1
Molecular Formula:
Molecular Weight: 469.491
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: acetic acid (3S,4R,3a'R,5'R,6'S,6a'R)-5'-{1-(4-methoxyphenyl)-4-oxo-3-phenoxyazetidin-2-yl}-2',2'-dimethyl-tetrahydrofuro[2',3'-d][1',3']dioxol-6'-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: acetic acid (3S,4R,3a'R,5'R,6'S,6a'R)-5'-{1-(4-methoxyphenyl)-4-oxo-3-phenoxyazetidin-2-yl}-2',2'-dimethyl-tetrahydrofuro[2',3'-d][1',3']dioxol-6'-yl ester(547769-47-1)
EPA Substance Registry System: acetic acid (3S,4R,3a'R,5'R,6'S,6a'R)-5'-{1-(4-methoxyphenyl)-4-oxo-3-phenoxyazetidin-2-yl}-2',2'-dimethyl-tetrahydrofuro[2',3'-d][1',3']dioxol-6'-yl ester(547769-47-1)

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: 547769-47-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 547769-47-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,4,7,7,6 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 547769-47:
(8*5)+(7*4)+(6*7)+(5*7)+(4*6)+(3*9)+(2*4)+(1*7)=211
211 % 10 = 1
So 547769-47-1 is a valid CAS Registry Number.

547769-47-1Upstream product

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547769-47-1Relevant academic research and scientific papers

Asymmetric synthesis of azetidin-2-ones by [2+2] cycloaddition using chiral imines derived from D-(+)-glucose

Arun,Joshi,Puranik,Bhawal,Deshmukh

, p. 2309 - 2316 (2003)

Asymmetric synthesis of β-lactams by the [2+2] cycloaddition of ketenes with chiral imines derived from D-(+)-glucose was carried out; predominantly cis-β-lactams were formed with very high diastereoselectivity. The stereochemistry at C-3 and C-4 was esta

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