Cas 855773-56-7,(+)-(3R,4S)-4-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-3-phenoxy-1-[(S)-2-hydroxy-4-pentenyl]-2-azetidinone

855773-56-7

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Basic information

Product Name: (+)-(3R,4S)-4-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-3-phenoxy-1-[(S)-2-hydroxy-4-pentenyl]-2-azetidinone
Synonyms: (+)-(3R,4S)-4-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-3-phenoxy-1-[(S)-2-hydroxy-4-pentenyl]-2-azetidinone
CAS NO:855773-56-7
Molecular Formula:
Molecular Weight: 347.411
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,4S)-4-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-3-phenoxy-1-[(S)-2-hydroxy-4-pentenyl]-2-azetidinone(CAS DataBase Reference)
NIST Chemistry Reference: (+)-(3R,4S)-4-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-3-phenoxy-1-[(S)-2-hydroxy-4-pentenyl]-2-azetidinone(855773-56-7)
EPA Substance Registry System: (+)-(3R,4S)-4-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-3-phenoxy-1-[(S)-2-hydroxy-4-pentenyl]-2-azetidinone(855773-56-7)

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: 855773-56-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 855773-56-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,5,7,7 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 855773-56:
(8*8)+(7*5)+(6*5)+(5*7)+(4*7)+(3*3)+(2*5)+(1*6)=217
217 % 10 = 7
So 855773-56-7 is a valid CAS Registry Number.

855773-56-7Upstream product

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855773-56-7Relevant academic research and scientific papers

Diastereoselective route to novel fused or bridged tricyclic β-lactams through intramolecular nitrone-alkene cycloaddition of 2-azetidinone-tethered alkenylaldehydes - Synthetic applications to carbacephams and cyclic β-amino acid derivatives

Alcaide, Benito,Saez, Elena

, p. 1680 - 1693 (2007/10/03)

A convenient, regio- and stereoselective direct route to optically pure unusually fused or bridged tricyclic β-lactams has been developed by use of intramolecular nitrone-alkene cycloaddition (INAC) reactions of easily available monocyclic 2-azetidinone-t

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