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1-(3-chlorophenyl)-3-prop-2-en-1-ylthiourea, also known as N-(3-chlorophenyl)-N'-prop-2-en-1-ylthiourea, is a chemical compound that belongs to the class of thioureas. It is characterized by a thiourea functional group, which consists of a sulfur atom joined to a carbon atom via a double bond. 1-(3-chlorophenyl)-3-prop-2-en-1-ylthiourea is known for its potential pharmacological and biological activities, as well as its applications in organic synthesis and as a reagent in chemical reactions.

14255-75-5

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14255-75-5 Usage

Uses

Used in Organic Synthesis:
1-(3-chlorophenyl)-3-prop-2-en-1-ylthiourea is used as a reagent in organic synthesis for the production of various chemical compounds. Its unique structure and properties make it a valuable molecule in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Chemical Reactions:
As a reagent, 1-(3-chlorophenyl)-3-prop-2-en-1-ylthiourea is utilized in a variety of chemical reactions to facilitate the formation of desired products. Its presence can enhance reaction rates, improve yields, and enable the synthesis of complex molecules that are otherwise difficult to obtain.
Used in Pharmaceutical Development:
1-(3-chlorophenyl)-3-prop-2-en-1-ylthiourea is studied for its potential pharmacological and biological activities. Its structure and properties make it a promising candidate for the development of new drugs and therapeutic agents, particularly in the areas of antifungal and antimicrobial treatments.
Used in Antifungal Applications:
In the field of antifungal research, 1-(3-chlorophenyl)-3-prop-2-en-1-ylthiourea is used as an active ingredient to combat fungal infections. Its ability to inhibit fungal growth makes it a valuable component in the development of antifungal medications and treatments.
Used in Antimicrobial Applications:
Similarly, 1-(3-chlorophenyl)-3-prop-2-en-1-ylthiourea is also explored for its antimicrobial properties. It can be used as an agent to fight against bacterial infections, contributing to the development of new antimicrobial drugs and therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 14255-75-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,5 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14255-75:
(7*1)+(6*4)+(5*2)+(4*5)+(3*5)+(2*7)+(1*5)=95
95 % 10 = 5
So 14255-75-5 is a valid CAS Registry Number.

14255-75-5SDS

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 1-(3-chlorophenyl)-3-prop-2-enylthiourea

1.2 Other means of identification

Product number -
Other names -

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

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More Details:14255-75-5 SDS

14255-75-5Relevant academic research and scientific papers

Enzymatic Oxidative Conversion of Thio to Oxo by Baker's Yeast in Thiocarbamates and Thioureas

Kamal, Ahmed,Rao, Maddamsetty V.,Rao, Adari B.

, p. 655 - 656 (2007/10/02)

The enzymatic conversion of aryl allylthiocarbamates and 1-allyl-3-arylthioureas by baker's yeast to the corresponding carbamates and ureas in good yields is described.

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