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372-20-3

372-20-3

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372-20-3 Usage

Chemical Properties

colourless to light yellow liquid

Uses

3-Fluorophenol is a reactant used in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 372-20-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,7 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 372-20:
(5*3)+(4*7)+(3*2)+(2*2)+(1*0)=53
53 % 10 = 3
So 372-20-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H5FO/c7-5-2-1-3-6(8)4-5/h1-4,8H

372-20-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Fluorophenol

1.2 Other means of identification

Product number -
Other names Phenol,3-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:372-20-3 SDS

372-20-3Relevant articles and documents

Process development and manufacture of potassium 2-fluoro-6-hydroxyphenyltrifluoroborate

Pawar, Lokesh,Jayaramaiah, Ramesh,Krishnan, Baburaj,Arunachalampillai, Athimoolam,Chen, Ying,Parsons, Andrew T.,Robinson, Jo Anna,Tedrow, Jason S.

, p. 4266 - 4270 (2019)

The development of a phase-appropriate manufacturing-scale synthesis of potassium 2-fluoro-6-hydroxyphenyltrifluoroborate was achieved. Investigations into improving the yield and robustness indicated that pH of the reaction medium is a critical process parameter. Additional development resulted in replacing tartaric acid with citric acid, resulting in improved process robustness and enabling scale-up to >10 kg.

Nickel Hydride Catalyzed Cleavage of Allyl Ethers Induced by Isomerization

Kathe, Prasad M.,Berkefeld, Andreas,Fleischer, Ivana

supporting information, p. 1629 - 1632 (2021/02/09)

This report discloses the deallylation of O - and N -allyl functional groups by using a combination of a Ni-H precatalyst and excess Bronsted acid. Key steps are the isomerization of the O - or N -allyl group through Ni-catalyzed double-bond migration followed by Bronsted acid induced O/N-C bond hydrolysis. A variety of functional groups are tolerated in this protocol, highlighting its synthetic value.

Synthesis method of fluorine-containing phenol structure compound

-

Paragraph 0021-0022, (2021/03/13)

The invention discloses a synthesis method of a fluorine-containing phenol structure compound, and belongs to the technical field of chemical synthesis. Fluorine-containing benzoic acid is subjected to a one-pot reaction in a solvent under the action of alkali to obtain fluorine-containing phenate, and fluorine-containing phenol is obtained after acid regulation and dissociation. The synthesis method has the advantages of rich, cheap and easily available raw material structure, short synthesis steps, mild reaction conditions, simple and convenient operation, high synthesis yield, good productquality, wide application range and the like, and is suitable for simple and efficient synthesis of various high-value and high-purity fluorine-containing phenol compounds.

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