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4-fluoro-2-methylbenzenethiol, with the chemical formula C7H7FS, is an organosulfur compound derived from hydrocarbons where a hydrogen atom is replaced by a sulfur atom. It is known for its strong aromatic aroma and unique structure, which includes a fluorine atom that may contribute to its potential applications in various fields.

845823-04-3

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845823-04-3 Usage

Uses

Used in Organic Chemistry:
4-fluoro-2-methylbenzenethiol is used as a reagent, solvent, and synthetic intermediate in organic chemistry due to its unique structure and properties.
Used in Pharmacology:
The presence of the fluorine atom in 4-fluoro-2-methylbenzenethiol makes it potentially interesting for applications in pharmacology, where it could be utilized in the development of new drugs or drug candidates.
Used in Material Science:
4-fluoro-2-methylbenzenethiol's unique structure and properties may also make it suitable for applications in material science, where it could be used in the synthesis of new materials or the modification of existing ones.
However, it is important to note that 4-fluoro-2-methylbenzenethiol, like other sulfur-containing compounds, should be handled with care due to its potential toxicity.

Check Digit Verification of cas no

The CAS Registry Mumber 845823-04-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,5,8,2 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 845823-04:
(8*8)+(7*4)+(6*5)+(5*8)+(4*2)+(3*3)+(2*0)+(1*4)=183
183 % 10 = 3
So 845823-04-3 is a valid CAS Registry Number.

845823-04-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Fluoro-2-methylbenzenethiol

1.2 Other means of identification

Product number -
Other names 4-Fluoro-2-methyl thiophenol

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:845823-04-3 SDS

845823-04-3Downstream Products

845823-04-3Relevant articles and documents

Solvent-free synthesis of thiophenol using uncatalyzed transfer hydrogenation

Zhou, Shaodong,Qian, Chao,Chen, Xinzhi

experimental part, p. 2432 - 2439 (2012/06/18)

Clean and sustainable transfer hydrogenation for aryl sulfonamides and sulfonyl chlorides is described. The protocol is chemoselective and uses neither catalyst nor solvent.

Catalytic transfer hydrogenation of aryl sulfo compounds

Chen, Xinzhi,Zhou, Shaodong,Qian, Chao

experimental part, p. 179 - 185 (2012/05/21)

A new method to reduce aryl sulfo compounds via transfer hydrogenation was investigated, using Pd/C as a catalyst, and 2-propanol or formic acid as hydrogen sources. This new process is simple and clean.

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