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(R)-(+)-3,3-DIFLUORO-1,2-HEPTANEDIOL is a chemical compound that belongs to the class of fluorinated alcohols. It is characterized by the presence of two fluorine atoms attached to the third and fourth carbon atoms of the heptyl chain, which makes it valuable in the development of fluorinated organic compounds. (R)-(+)-3,3-DIFLUORO-1,2-HEPTANEDIOL is also utilized as a chiral auxiliary for asymmetric synthesis and serves as a resolving agent for racemic mixtures. Its unique structure and properties have garnered interest in the field of medicinal chemistry and potential applications in the production of novel materials.

158358-96-4

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158358-96-4 Usage

Uses

Used in Pharmaceutical Industry:
(R)-(+)-3,3-DIFLUORO-1,2-HEPTANEDIOL is used as a building block for the production of various pharmaceuticals. Its unique fluorinated structure contributes to the development of new drugs with improved properties, such as enhanced bioavailability and selectivity.
Used in Agrochemical Industry:
In the agrochemical industry, (R)-(+)-3,3-DIFLUORO-1,2-HEPTANEDIOL is used as a key component in the synthesis of agrochemicals. Its incorporation into these compounds can lead to improved performance and selectivity in agricultural applications.
Used in Fine Chemicals Production:
(R)-(+)-3,3-DIFLUORO-1,2-HEPTANEDIOL is also used as a building block for the production of other fine chemicals. Its fluorinated nature allows for the creation of specialty chemicals with specific properties tailored for various applications.
Used in Asymmetric Synthesis:
(R)-(+)-3,3-DIFLUORO-1,2-HEPTANEDIOL is used as a chiral auxiliary in asymmetric synthesis. Its presence can help achieve higher enantioselectivity and yield in the synthesis of chiral compounds, which are essential in the pharmaceutical and chemical industries.
Used in Racemic Mixture Resolution:
As a resolving agent for racemic mixtures, (R)-(+)-3,3-DIFLUORO-1,2-HEPTANEDIOL aids in the separation of enantiomers, which is crucial for obtaining pure chiral compounds with specific biological activities.
Used in Novel Materials Production:
(R)-(+)-3,3-DIFLUORO-1,2-HEPTANEDIOL has potential applications in the production of novel materials due to its unique structure and properties. It can be used to develop new materials with enhanced characteristics for various industries, including electronics, automotive, and aerospace.

Check Digit Verification of cas no

The CAS Registry Mumber 158358-96-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,3,5 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 158358-96:
(8*1)+(7*5)+(6*8)+(5*3)+(4*5)+(3*8)+(2*9)+(1*6)=174
174 % 10 = 4
So 158358-96-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H14F2O2/c1-2-3-4-7(8,9)6(11)5-10/h6,10-11H,2-5H2,1H3/t6-/m1/s1

158358-96-4 Well-known Company Product Price

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  • Aldrich

  • (477427)  (R)-(+)-3,3-Difluoro-1,2-heptanediol  95%

  • 158358-96-4

  • 477427-250MG

  • 2,419.56CNY

  • Detail

158358-96-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-3,3-difluoroheptane-1,2-diol

1.2 Other means of identification

Product number -
Other names (2R)-3,3-difluoroheptan-1,2-diol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:158358-96-4 SDS

158358-96-4Relevant academic research and scientific papers

Stereoselective synthesis of 14,14-difluorocoriolic acid

Kornilov, Andrew M.,Sorochinsky, Alexander E.,Kukhar, Valery P.

, p. 1015 - 1018 (1994)

An efficient, stereoselective synthesis of (R)-14,14-difluoro-13-hydroxy-9(Z),11(E)-octadecadienoic acid ((R)-14,14-difluorocoriolic acid) 2 starting from D-glyceraldehyde acetonide via the key intermediate (R)-3,3-difluoro-1,2-dihydroxyheptane 9 is repor

Selective incorporation of CF2-group into the natural compounds molecules. Synthesis of 14,14-difluorocoriolic acid

Kornilov,Kulik,Sorochinsky,Kukhar

, p. 199 - 206 (2007/10/02)

The difluorides obtained in the reaction of DAST with appropriate ketones could serve as suitable starting materials for the selective incorporation of CF2-group into the molecules of the unsaturated chiral natural compounds. As an example, ste

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