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19182-34-4

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19182-34-4 Usage

Description

(4-fluorophenyl)carbamodithioic acid, with the chemical formula C7H6FNS2, is a derivative of carbamodithioic acid that features a 4-fluorophenyl group. (4-fluorophenyl)carbamodithioic acid is recognized for its potential biological activities and is being studied for its possible applications in therapeutics.

Uses

Used in Pharmaceutical Synthesis:
(4-fluorophenyl)carbamodithioic acid is utilized as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows it to be incorporated into drug molecules, potentially enhancing their efficacy and selectivity for specific biological targets.
Used in Agrochemical Production:
(4-fluorophenyl)carbamodithioic acid also finds application in the production of agrochemicals, where it can be used to develop new pesticides or herbicides. Its incorporation into these products may improve their effectiveness in controlling pests and weeds while minimizing environmental impact.
Used as a Reagent in Organic Chemistry:
(4-fluorophenyl)carbamodithioic acid serves as a valuable reagent in organic chemistry, facilitating various chemical reactions and synthesis processes. Its presence can influence reaction outcomes and provide access to a range of novel organic compounds.
Used in Therapeutic Applications:
Due to its potential biological activities, (4-fluorophenyl)carbamodithioic acid is being explored for use in therapeutic applications. While further research is needed to fully understand its capabilities, it holds promise for contributing to the development of new treatments for various conditions.
It is crucial to handle (4-fluorophenyl)carbamodithioic acid with care, as it may present health risks if not properly managed. Safety precautions should be taken to mitigate any potential hazards associated with this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 19182-34-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,8 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19182-34:
(7*1)+(6*9)+(5*1)+(4*8)+(3*2)+(2*3)+(1*4)=114
114 % 10 = 4
So 19182-34-4 is a valid CAS Registry Number.

19182-34-4SDS

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 azane,(4-fluorophenyl)carbamodithioic acid

1.2 Other means of identification

Product number -
Other names ammonium p-fluorophenyldithiocarbamate

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:19182-34-4 SDS

19182-34-4Relevant articles and documents

Synthesis and antimicrobial activity of some new 1,2,4-trizoles

Jain, Rakesh Kumar,Mishra, Vikash Kumar,Kashaw, Varsha

, p. 1317 - 1322 (2017/05/02)

A series of 1,2,4-triazole derivatives were synthesized using appropriate synthetic route and structures were confirmed by IR,1H NMR and elemental analysis. All the synthesized compounds (6a-6h and 7a-7h) were evaluated for antimicrobial activity by determining their minimum inhibitory concentrations (MICs) against a panel of Gram-positive, Gram-negative bacteria and fungi. Most of the compounds showed significant antimicrobial activity against Gram-positive bacteria viz. S. aureus, B. subtilis, Gram-negative bacteria viz. E. coli, P. aerugenosa and fungi viz. C. albicans, A. niger. Some of the compounds showed better antibacterial activities against Gram-positive bacteria compared to Gram-negative bacteria. Compounds 7g, 6g, 6a exhibited good MICs against Gram-positive bacteria and 7f showed better MICs against Gram-negative bacteria compared to reference norfloxacin. Compounds 7f and 7d exhibited MICs which is equipotent to the reference drug ketoconazole.

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