Cas 354580-08-8,4-Benzenesulfonyl-5-((R)-9-isopropenyl-6-methyl-1,4-dioxa-spiro[4.5]dec-6-yl)-pentan-2-one

354580-08-8

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Basic information

Product Name: 4-Benzenesulfonyl-5-((R)-9-isopropenyl-6-methyl-1,4-dioxa-spiro[4.5]dec-6-yl)-pentan-2-one
Synonyms:
CAS NO:354580-08-8
Molecular Formula:
Molecular Weight: 420.57
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: 4-Benzenesulfonyl-5-((R)-9-isopropenyl-6-methyl-1,4-dioxa-spiro[4.5]dec-6-yl)-pentan-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 4-Benzenesulfonyl-5-((R)-9-isopropenyl-6-methyl-1,4-dioxa-spiro[4.5]dec-6-yl)-pentan-2-one(354580-08-8)
EPA Substance Registry System: 4-Benzenesulfonyl-5-((R)-9-isopropenyl-6-methyl-1,4-dioxa-spiro[4.5]dec-6-yl)-pentan-2-one(354580-08-8)

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: 354580-08-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 354580-08-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,4,5,8 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 354580-08:
(8*3)+(7*5)+(6*4)+(5*5)+(4*8)+(3*0)+(2*0)+(1*8)=148
148 % 10 = 8
So 354580-08-8 is a valid CAS Registry Number.

354580-08-8Upstream product

108270-19-5 3-iodo-2-(methoxymethyloxy)-1-propene

354580-08-8Downstream Products

354580-10-2 (2S,5R)-5-Isopropenyl-2-methyl-2-((E)-4-oxo-pent-2-enyl)-cyclohexanone

354580-08-8Relevant academic research and scientific papers

Application of the tandem Stryker reduction-aldol cyclization strategy to the asymmetric synthesis of lucinone

Chiu, Pauline,Szeto, Chun Pong,Geng, Zhe,Cheng, Kin Fai

, p. 4091 - 4093 (2001)

The tandem conjugate reduction-aldol cyclization using Stryker's reagent has been employed as the key-step in an asymmetric total synthesis of lucinone.

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