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7-Fluoroheptanoic acid is a synthetic organic compound characterized by the molecular formula C7H13FO2. It is a fluorinated derivative of heptanoic acid, with a fluorine atom replacing one of the hydrogen atoms in the molecule. This seven-carbon chain carboxylic acid is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, where the introduction of fluorine can significantly alter the physical and chemical properties of the molecule, such as its lipophilicity and metabolic stability. The compound is typically used as an intermediate in the preparation of more complex molecules, and its properties make it a valuable building block in the development of new drugs and chemical products.

334-28-1

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334-28-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 334-28-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,3 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 334-28:
(5*3)+(4*3)+(3*4)+(2*2)+(1*8)=51
51 % 10 = 1
So 334-28-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H13FO2/c8-6-4-2-1-3-5-7(9)10/h1-6H2,(H,9,10)

334-28-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-Fluoroheptanoic acid

1.2 Other means of identification

Product number -
Other names Heptanoic acid, 7-fluoro-

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:334-28-1 SDS

334-28-1Relevant academic research and scientific papers

Silver-catalyzed radical fluorination of alkylboronates in aqueous solution

Li, Zhaodong,Wang, Zhentao,Zhu, Lin,Tan, Xinqiang,Li, Chaozhong

supporting information, p. 16439 - 16443 (2015/01/09)

We report herein an efficient and general method for the deboronofluorination of alkylboronates. Thus, with the catalysis of AgNO3, the reactions of various alkylboronic acids or their pinacol esters with Selectfluor reagent in acidic aqueous solution afforded the corresponding alkyl fluorides under mild conditions. A broad substrate scope and wide functional group compatibility were observed. A radical mechanism is proposed for this site-specific fluorination.

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