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8-Fluoro-3,3-dimethyloctanoic acid is a synthetic organic compound characterized by its molecular formula C10H17FO2. 8-Fluoro-3,3-dimethyloctanoic acid features a fluorine atom at the 8th carbon position, two methyl groups attached to the 3rd carbon, and a carboxylic acid functional group at the end of the octanoic acid chain. It is a colorless liquid with a molecular weight of approximately 190.24 g/mol. The presence of the fluorine atom imparts unique properties to the molecule, such as increased lipophilicity and potential reactivity, which can be exploited in various chemical and pharmaceutical applications. Due to its specific structure, 8-fluoro-3,3-dimethyloctanoic acid may be used as an intermediate in the synthesis of more complex molecules or as a building block in the development of new drugs and materials.

333-33-5

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333-33-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 333-33-5 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 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 333-33:
(5*3)+(4*3)+(3*3)+(2*3)+(1*3)=45
45 % 10 = 5
So 333-33-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H19FO2/c1-10(2,6-3-4-8-11)7-5-9(12)13/h3-8H2,1-2H3,(H,12,13)

333-33-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-fluoro-4,4-dimethyloctanoic acid

1.2 Other means of identification

Product number -
Other names OCTANOIC ACID,3,3-DIMETHYL-8-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:333-33-5 SDS

333-33-5Downstream Products

333-33-5Relevant academic research and scientific papers

Synthesis of ω-fluorinated octanoic acid and its β-substituted derivatives

Nagatsuki, Fumi,Sasaki, Shigeki,Maeda, Minoru

, p. 373 - 383 (2007/10/02)

Simple syntheses are described for the ω-fluorinated analogs of octanoic acid and its β-substituted derivatives in which insertion of a methyl and dimethyl group, and oxygen substitution at the C-3 position are involved, employing nucleophilic displacement with fluoride ion of the tosylate functions in the later stage of synthesis.The synthetic procedures offer easy and convenient acces to the corresponding 18F-labeled analogs using the readily available fluoride ion.

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