Cas 1415692-11-3,(3R,4R)-4-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)-1-(4-methoxyphenyl)-3-(1H-pyrrol-1-yl)azetidin-2-one

1415692-11-3

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Basic information

Product Name: (3R,4R)-4-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)-1-(4-methoxyphenyl)-3-(1H-pyrrol-1-yl)azetidin-2-one
Synonyms: (3R,4R)-4-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)-1-(4-methoxyphenyl)-3-(1H-pyrrol-1-yl)azetidin-2-one
CAS NO:1415692-11-3
Molecular Formula:
Molecular Weight: 342.395
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: (3R,4R)-4-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)-1-(4-methoxyphenyl)-3-(1H-pyrrol-1-yl)azetidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (3R,4R)-4-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)-1-(4-methoxyphenyl)-3-(1H-pyrrol-1-yl)azetidin-2-one(1415692-11-3)
EPA Substance Registry System: (3R,4R)-4-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)-1-(4-methoxyphenyl)-3-(1H-pyrrol-1-yl)azetidin-2-one(1415692-11-3)

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: 1415692-11-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1415692-11-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,6,9 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1415692-11:
(9*1)+(8*4)+(7*1)+(6*5)+(5*6)+(4*9)+(3*2)+(2*1)+(1*1)=153
153 % 10 = 3
So 1415692-11-3 is a valid CAS Registry Number.

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1415692-11-3Relevant academic research and scientific papers

Novel synthesis of 3-pyrrole substituted β-lactams via microwave-induced bismuth nitrate-catalyzed reaction

Bandyopadhyay, Debasish,Cruz, Jessica,Banik, Bimal K.

, p. 10686 - 10695 (2012)

Highly stereoselective synthesis of 3-pyrrole substituted β-lactams is accomplished. The first step involves the synthesis of 3-phthalimido substituted β-lactams following Staudinger cycloaddition reaction of acid chloride equivalent with imines. Synthesi

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