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(S)-(-)-1,1,1-TRIFLUOROHEPTAN-2-OL, also known as (S)-(-)-2-Trifluoromethyl-1-heptanol, is a chemical compound characterized by its molecular formula C7H13F3O. It is a clear, colorless liquid with a slightly sweet odor. (S)-(-)-1,1,1-TRIFLUOROHEPTAN-2-OL is recognized for its versatility in organic chemistry, serving as a crucial intermediate in the synthesis of pharmaceuticals and agrochemicals, a chiral auxiliary in asymmetric synthesis, a building block in the preparation of fluorinated organic compounds, and a solvent in organic reactions.

130025-35-3

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130025-35-3 Usage

Uses

Used in Pharmaceutical Industry:
(S)-(-)-1,1,1-TRIFLUOROHEPTAN-2-OL is used as an intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and medicines. Its unique properties allow for the creation of complex molecular structures that can target specific biological pathways, potentially leading to more effective treatments.
Used in Agrochemical Industry:
In the agrochemical sector, (S)-(-)-1,1,1-TRIFLUOROHEPTAN-2-OL is utilized as an intermediate for the synthesis of agrochemicals, which are essential for enhancing crop protection and yield. Its role in this industry is vital for the development of innovative and efficient products that can address various agricultural challenges.
Used in Asymmetric Synthesis:
(S)-(-)-1,1,1-TRIFLUOROHEPTAN-2-OL is employed as a chiral auxiliary in asymmetric synthesis, a technique that is crucial for producing enantiomerically pure compounds. This application is particularly important in the pharmaceutical industry, where the desired biological activity is often associated with a specific enantiomer.
Used in Fluorinated Organic Compounds Preparation:
As a building block, (S)-(-)-1,1,1-TRIFLUOROHEPTAN-2-OL is used in the preparation of fluorinated organic compounds. Fluorination can significantly alter the properties of organic molecules, making them more stable, reactive, or bioavailable, which is valuable in various chemical and pharmaceutical applications.
Used as a Solvent in Organic Reactions:
(S)-(-)-1,1,1-TRIFLUOROHEPTAN-2-OL also serves as a solvent in organic reactions, facilitating the process and improving the yield of desired products. Its properties as a solvent make it suitable for a range of chemical processes, contributing to the efficiency and effectiveness of organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 130025-35-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,0,2 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 130025-35:
(8*1)+(7*3)+(6*0)+(5*0)+(4*2)+(3*5)+(2*3)+(1*5)=63
63 % 10 = 3
So 130025-35-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H13F3O/c1-2-3-4-5-6(11)7(8,9)10/h6,11H,2-5H2,1H3/t6-/m0/s1

130025-35-3 Well-known Company Product Price

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  • Aldrich

  • (532525)  (S)-(−)-1,1,1-Trifluoroheptan-2-ol  97%

  • 130025-35-3

  • 532525-1G

  • 1,291.68CNY

  • Detail

130025-35-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-1,1,1-trifluoroheptan-2-ol

1.2 Other means of identification

Product number -
Other names PC0644

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:130025-35-3 SDS

130025-35-3Downstream Products

130025-35-3Relevant academic research and scientific papers

TRIFLUOROPROPENE OXIDE AS A TRIFLUOROMETHYL SOURCE. PREPARATION OF OPTICALLY ACTIVE ALCOHOLS

Takahashi, Osamu,Furuhashi, Keizo,Fukumasa, Mitsuo,Hirai, Toshihiro

, p. 7031 - 7034 (2007/10/02)

Optically active 3,3,3-trifluoropropene oxide (TFPO) was converted to 1,1,1-trifluoro-2-ols via Grignard type or Friedel-Crafts type reaction.The regio-selectivity of the latter reaction was discussed through an MO calculation.

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