Cas 139357-01-0,2-{(R)-3-[(2R,4R)-4-(2-Chloro-phenyl)-5,5-dimethyl-[1,3]dioxan-2-yl]-cyclohex-2-enyl}-malonic acid dimethyl ester

139357-01-0

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Basic information

Product Name: 2-{(R)-3-[(2R,4R)-4-(2-Chloro-phenyl)-5,5-dimethyl-[1,3]dioxan-2-yl]-cyclohex-2-enyl}-malonic acid dimethyl ester
Synonyms:
CAS NO:139357-01-0
Molecular Formula:
Molecular Weight: 436.933
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: 2-{(R)-3-[(2R,4R)-4-(2-Chloro-phenyl)-5,5-dimethyl-[1,3]dioxan-2-yl]-cyclohex-2-enyl}-malonic acid dimethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-{(R)-3-[(2R,4R)-4-(2-Chloro-phenyl)-5,5-dimethyl-[1,3]dioxan-2-yl]-cyclohex-2-enyl}-malonic acid dimethyl ester(139357-01-0)
EPA Substance Registry System: 2-{(R)-3-[(2R,4R)-4-(2-Chloro-phenyl)-5,5-dimethyl-[1,3]dioxan-2-yl]-cyclohex-2-enyl}-malonic acid dimethyl ester(139357-01-0)

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: 139357-01-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 139357-01-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,3,5 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 139357-01:
(8*1)+(7*3)+(6*9)+(5*3)+(4*5)+(3*7)+(2*0)+(1*1)=140
140 % 10 = 0
So 139357-01-0 is a valid CAS Registry Number.

139357-01-0Upstream product

108-59-8 malonic acid dimethyl ester

139357-01-0Downstream Products

139357-01-0Relevant academic research and scientific papers

Near Absolute Regio-, Diastereo-, and Enantioselectivity in a Palladium Catalyzed Alkylation Using an Uncommon Chiral Auxiliary

Sjouken, Ronald,Ebens, Rijko,Kellogg, Richard M.

, p. 56 - 58 (1992)

Condensation of R-(+)-1-(2-chlorophenyl)-2,2-dimethyl-propan-1,3-diol (2) with a derivative (1) of 1-formylcyclohexene substituted in the 3-position with an acetoxy group proceeded with absolute stereospecificity at the acetal center.Catalytic alkylation of the ?-allyl complex obtained upon reaction with Pd with the anion of dimethylmalonate proceeded at the 3-position of the cyclohexyl ring with complete stereocontrol.

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