Cas 432504-77-3,(3S,5S,8R,9S)-3-isopropyl-9-methyl-7,7,8-triphenyl-8,9-epoxy-1,6-dioxa-4-azaspiro[4.4]nonane

432504-77-3

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Basic information

Product Name: (3S,5S,8R,9S)-3-isopropyl-9-methyl-7,7,8-triphenyl-8,9-epoxy-1,6-dioxa-4-azaspiro[4.4]nonane
Synonyms: (3S,5S,8R,9S)-3-isopropyl-9-methyl-7,7,8-triphenyl-8,9-epoxy-1,6-dioxa-4-azaspiro[4.4]nonane
CAS NO:432504-77-3
Molecular Formula:
Molecular Weight: 427.543
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: (3S,5S,8R,9S)-3-isopropyl-9-methyl-7,7,8-triphenyl-8,9-epoxy-1,6-dioxa-4-azaspiro[4.4]nonane(CAS DataBase Reference)
NIST Chemistry Reference: (3S,5S,8R,9S)-3-isopropyl-9-methyl-7,7,8-triphenyl-8,9-epoxy-1,6-dioxa-4-azaspiro[4.4]nonane(432504-77-3)
EPA Substance Registry System: (3S,5S,8R,9S)-3-isopropyl-9-methyl-7,7,8-triphenyl-8,9-epoxy-1,6-dioxa-4-azaspiro[4.4]nonane(432504-77-3)

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: 432504-77-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 432504-77-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,2,5,0 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 432504-77:
(8*4)+(7*3)+(6*2)+(5*5)+(4*0)+(3*4)+(2*7)+(1*7)=123
123 % 10 = 3
So 432504-77-3 is a valid CAS Registry Number.

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432504-77-3Relevant academic research and scientific papers

Stereospecific beta-lithiation of oxazolinyloxiranes: synthesis of alpha,beta-epoxy-gamma-butyrolactones.

Capriati, Vito,Degennaro, Leonardo,Favia, Raffaele,Florio, Saverio,Luisi, Renzo

, p. 1551 - 1554 (2007/10/03)

[reaction: see text]. Stereospecific beta-lithiation of beta-aryl-substituted oxazolinyloxiranes is described. The trapping reaction of such reactive intermediates with carbonyl compounds gave alpha,beta-epoxy-gamma-butyrolactones after deblocking of the

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