Cas 755031-13-1,Cyclohexanol, 3-[[2-(4-fluorophenyl)-5-methyl-4-oxazolyl]methoxy]-, acetate (ester), (1R,3S)-

755031-13-1

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Basic information

Product Name: Cyclohexanol, 3-[[2-(4-fluorophenyl)-5-methyl-4-oxazolyl]methoxy]-, acetate (ester), (1R,3S)-
Synonyms:
CAS NO:755031-13-1
Molecular Formula: C19H22FNO4
Molecular Weight: 347.386
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: Cyclohexanol, 3-[[2-(4-fluorophenyl)-5-methyl-4-oxazolyl]methoxy]-, acetate (ester), (1R,3S)-(CAS DataBase Reference)
NIST Chemistry Reference: Cyclohexanol, 3-[[2-(4-fluorophenyl)-5-methyl-4-oxazolyl]methoxy]-, acetate (ester), (1R,3S)-(755031-13-1)
EPA Substance Registry System: Cyclohexanol, 3-[[2-(4-fluorophenyl)-5-methyl-4-oxazolyl]methoxy]-, acetate (ester), (1R,3S)-(755031-13-1)

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: 755031-13-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 755031-13-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,5,0,3 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 755031-13:
(8*7)+(7*5)+(6*5)+(5*0)+(4*3)+(3*1)+(2*1)+(1*3)=141
141 % 10 = 1
So 755031-13-1 is a valid CAS Registry Number.

755031-13-1Upstream product

108-05-4 vinyl acetate

755031-13-1Downstream Products

755031-13-1Relevant academic research and scientific papers

Process for preparing the enantiomeric forms of cis-configured 1,3-cyclohexanediol derivatives

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Page 16, (2010/02/08)

Process for preparing the enantiomeric forms of cis-configured 1,3-cyclohexanediol derivatives A process is described for preparing chiral, nonracemic, cis-configured 1,3-disubstituted cyclohexanols of the formula (I) where the radicals are as defined, by

Cycloalkyl derivatives having bioisosteric carboxylic acid groups, processes for their preparation and their use as pharmaceuticals

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Page 24-25, (2008/06/13)

Cycloalkyl derivatives having bioisosteric carboxylic acid groups, processes for their preparation and their use as pharmaceuticals The invention relates to cycloalkyl derivatives having bioisosteric carboxylic acid groups and to their physiologically acceptable salts and physiologically functional derivatives. What is described are compounds of the formula 1, in which the radicals are as defined, and their physiologically acceptable salts and processes for their preparations. The compounds are suitable for the treatment and/or prevention of disorders of fatty acid metabolism and glucose utilization disorders as well as of disorders in which insulin resistence is involved.

Arylcycloalkyl-substituted alkanoic acid derivatives, processes for their preparation and their use as pharmaceuticals

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Page/Page column 28-29, (2008/06/13)

Arylcycloalkyl-substituted alkanoic acid derivatives, processes for their preparation and their use as pharmaceuticals The invention relates to arylcycloalkyl-substituted alkanoic acid derivatives and to their physiologically acceptable salts and physiologically functional derivatives. What is described are compounds of the formula I, 1 in which the radicals are as defined, and their physiologically acceptable salts and processes for their preparation. The compounds are suitable, for example, for the treatment and/or prevention of disorders of the fatty acid metabolism and glucose utilization disorders and also disorders in which insulin resistance is involved.

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