Cas 524935-96-4,(3R,4S)-3-propargyloxy-4-[(R)-1-hydroxy-2-(1-cyclopentenyl)-ethyl]-1-(p-methoxyphenyl)-2-azetidinone

524935-96-4

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Basic information

Product Name: (3R,4S)-3-propargyloxy-4-[(R)-1-hydroxy-2-(1-cyclopentenyl)-ethyl]-1-(p-methoxyphenyl)-2-azetidinone
Synonyms: (3R,4S)-3-propargyloxy-4-[(R)-1-hydroxy-2-(1-cyclopentenyl)-ethyl]-1-(p-methoxyphenyl)-2-azetidinone
CAS NO:524935-96-4
Molecular Formula:
Molecular Weight: 341.407
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)-3-propargyloxy-4-[(R)-1-hydroxy-2-(1-cyclopentenyl)-ethyl]-1-(p-methoxyphenyl)-2-azetidinone(CAS DataBase Reference)
NIST Chemistry Reference: (3R,4S)-3-propargyloxy-4-[(R)-1-hydroxy-2-(1-cyclopentenyl)-ethyl]-1-(p-methoxyphenyl)-2-azetidinone(524935-96-4)
EPA Substance Registry System: (3R,4S)-3-propargyloxy-4-[(R)-1-hydroxy-2-(1-cyclopentenyl)-ethyl]-1-(p-methoxyphenyl)-2-azetidinone(524935-96-4)

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: 524935-96-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 524935-96-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,2,4,9,3 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 524935-96:
(8*5)+(7*2)+(6*4)+(5*9)+(4*3)+(3*5)+(2*9)+(1*6)=174
174 % 10 = 4
So 524935-96-4 is a valid CAS Registry Number.

524935-96-4Upstream product

1528-30-9 methylenecyclopentane

524935-96-4Downstream Products

524936-22-9 (3R,4S)-3-propargyloxy-4-[(R)-1-hydroxy-2-(1-cyclopentenyl)-ethyl]-1-(p-methoxyphenyl)-2-azetidinone methanesulfonate

524935-96-4Relevant academic research and scientific papers

Lewis acid-promoted intermolecular carbonyl-ene reaction of enantiopure 4-oxoazetidine-2-carbaldehydes. Rapid entry to novel fused polycyclic β-lactams

Alcaide, Benito,Almendros, Pedro,Pardo, Carmen,Rodriguez-Ranera, Carolina,Rodriguez-Vicente, Alberto

, p. 3106 - 3111 (2003)

Lewis acid-promoted carbonyl-ene reaction of enantiomerically pure 4-oxoazetidine-2-carbaldehydes with various activated alkenes gives 4-[(1′-hydroxy)homoallyl]-β-lactams with a very high level of syn diastereofacial selectivity. The above homoallylic alc

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