Cas 723336-98-9,(3R,4S,5E)-4-methyl-1-phenyl-3-{[(1R)-1-(2,4,6-triisopropylphenyl)ethyl]oxy}hept-5-en-1-one

723336-98-9

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Basic information

Product Name: (3R,4S,5E)-4-methyl-1-phenyl-3-{[(1R)-1-(2,4,6-triisopropylphenyl)ethyl]oxy}hept-5-en-1-one
Synonyms: (3R,4S,5E)-4-methyl-1-phenyl-3-{[(1R)-1-(2,4,6-triisopropylphenyl)ethyl]oxy}hept-5-en-1-one
CAS NO:723336-98-9
Molecular Formula:
Molecular Weight: 448.689
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,5E)-4-methyl-1-phenyl-3-{[(1R)-1-(2,4,6-triisopropylphenyl)ethyl]oxy}hept-5-en-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (3R,4S,5E)-4-methyl-1-phenyl-3-{[(1R)-1-(2,4,6-triisopropylphenyl)ethyl]oxy}hept-5-en-1-one(723336-98-9)
EPA Substance Registry System: (3R,4S,5E)-4-methyl-1-phenyl-3-{[(1R)-1-(2,4,6-triisopropylphenyl)ethyl]oxy}hept-5-en-1-one(723336-98-9)

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: 723336-98-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 723336-98-9 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 8 respectively.
Calculate Digit Verification of CAS Registry Number 723336-98:
(8*7)+(7*2)+(6*3)+(5*3)+(4*3)+(3*6)+(2*9)+(1*8)=159
159 % 10 = 9
So 723336-98-9 is a valid CAS Registry Number.

723336-98-9Upstream product

13735-81-4 1-styrenyloxytrimethylsilane

723336-98-9Downstream Products

723337-03-9 (E)-(3R,4S)-3-Hydroxy-4-methyl-1-phenyl-hept-5-en-1-one

723336-98-9Relevant 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 (2007/10/03)

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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