Cas 514205-01-7,(2R,3S,4S)-4-(dimethylthexylsilyl)oxy-3-O-methoxymethyl-2,3-dihydroxy-2-methyl-5-cyclohexen-1-one

514205-01-7

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Basic information

Product Name: (2R,3S,4S)-4-(dimethylthexylsilyl)oxy-3-O-methoxymethyl-2,3-dihydroxy-2-methyl-5-cyclohexen-1-one
Synonyms: (2R,3S,4S)-4-(dimethylthexylsilyl)oxy-3-O-methoxymethyl-2,3-dihydroxy-2-methyl-5-cyclohexen-1-one
CAS NO:514205-01-7
Molecular Formula:
Molecular Weight: 344.524
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: (2R,3S,4S)-4-(dimethylthexylsilyl)oxy-3-O-methoxymethyl-2,3-dihydroxy-2-methyl-5-cyclohexen-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3S,4S)-4-(dimethylthexylsilyl)oxy-3-O-methoxymethyl-2,3-dihydroxy-2-methyl-5-cyclohexen-1-one(514205-01-7)
EPA Substance Registry System: (2R,3S,4S)-4-(dimethylthexylsilyl)oxy-3-O-methoxymethyl-2,3-dihydroxy-2-methyl-5-cyclohexen-1-one(514205-01-7)

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: 514205-01-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 514205-01-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,4,2,0 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 514205-01:
(8*5)+(7*1)+(6*4)+(5*2)+(4*0)+(3*5)+(2*0)+(1*1)=97
97 % 10 = 7
So 514205-01-7 is a valid CAS Registry Number.

514205-01-7Upstream product

514205-01-7Downstream Products

514205-01-7Relevant academic research and scientific papers

Chemoenzymatic synthesis of chiral enones from aromatic compounds

Schapiro, Valeria,Cavalli, Gabriel,Seoane, Gustavo A.,Faccio, Ricardo,Mombru, Alvaro W.

, p. 2453 - 2459 (2007/10/03)

A series of chiral enones was successfully synthesized from chemoenzymatically produced chiral diols. These chiral enones are highly functionalized synthons, which can be used in the total synthesis of natural products such as forskolin and avermectins.

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