Cas 723336-96-7,(4R,5S,6S,7E)-5-{[(1R)-1-(2,4,6-triisopropylphenyl)ethyl]oxy}-4,6-dimethylnon-7-en-3-one

723336-96-7

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Basic information

Product Name: (4R,5S,6S,7E)-5-{[(1R)-1-(2,4,6-triisopropylphenyl)ethyl]oxy}-4,6-dimethylnon-7-en-3-one
Synonyms: (4R,5S,6S,7E)-5-{[(1R)-1-(2,4,6-triisopropylphenyl)ethyl]oxy}-4,6-dimethylnon-7-en-3-one
CAS NO:723336-96-7
Molecular Formula:
Molecular Weight: 414.672
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: (4R,5S,6S,7E)-5-{[(1R)-1-(2,4,6-triisopropylphenyl)ethyl]oxy}-4,6-dimethylnon-7-en-3-one(CAS DataBase Reference)
NIST Chemistry Reference: (4R,5S,6S,7E)-5-{[(1R)-1-(2,4,6-triisopropylphenyl)ethyl]oxy}-4,6-dimethylnon-7-en-3-one(723336-96-7)
EPA Substance Registry System: (4R,5S,6S,7E)-5-{[(1R)-1-(2,4,6-triisopropylphenyl)ethyl]oxy}-4,6-dimethylnon-7-en-3-one(723336-96-7)

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: 723336-96-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 723336-96-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,3,3,3 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 723336-96:
(8*7)+(7*2)+(6*3)+(5*3)+(4*3)+(3*6)+(2*9)+(1*6)=157
157 % 10 = 7
So 723336-96-7 is a valid CAS Registry Number.

723336-96-7Upstream product

51425-54-8 (Z)-3-trimethylsiloxy-2-pentene

723336-96-7Downstream Products

723336-96-7Relevant academic research and scientific papers

Palladium-catalyzed conversion of β,γ-unsaturated silyl sulfinates into (E)-alkenes: Asymmetric synthesis of polypropionate fragments

Huang, Xiaogen,Craita, Cotinica,Vogel, Pierre

, p. 4272 - 4275 (2004)

At low temperature, 1-alkoxy-1,3-dienes add to sulfur dioxide activated by a Lewis or protic acid generating zwitterionic intermediates that can be quenched by enoxysilanes. The resulting β,γ-unsaturated silyl sulfinates can be desilylated by 1:1 Pd(OAc)

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