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1-(3-methoxyphenyl)-3-phenylthiourea, a member of the thiourea group, is a white solid chemical compound with a molecular formula of C14H14N2OS and a molar mass of 258.34 g/mol. It is recognized for its potential as an enzyme inhibitor and has been explored for its pharmacological properties, which include anticancer and antibacterial activities. Additionally, it has been investigated for applications in materials science and as a precursor in the synthesis of other organic compounds.

31090-81-0

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31090-81-0 Usage

Uses

Used in Organic Chemistry:
1-(3-methoxyphenyl)-3-phenylthiourea is used as a reagent and catalyst in organic chemistry for various reactions due to its unique chemical properties and reactivity.
Used in Pharmaceutical Research:
1-(3-methoxyphenyl)-3-phenylthiourea is used as a potential inhibitor for various enzymes, making it a candidate for the development of new drugs targeting enzyme-related diseases.
Used in Anticancer Applications:
1-(3-methoxyphenyl)-3-phenylthiourea is being studied for its potential as an anticancer agent, with the aim of developing new treatments for cancer patients.
Used in Antibacterial Applications:
1-(3-methoxyphenyl)-3-phenylthiourea is also being investigated for its potential antibacterial properties, which could lead to the development of new antibiotics to combat bacterial infections.
Used in Materials Science:
1-(3-methoxyphenyl)-3-phenylthiourea has been explored for its potential uses in materials science, where its unique properties may contribute to the development of new materials with specific characteristics.
Used as a Precursor in Synthesis:
1-(3-methoxyphenyl)-3-phenylthiourea serves as a precursor in the synthesis of other organic compounds, expanding its utility in the field of organic chemistry and potentially leading to the creation of novel molecules with various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 31090-81-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,0,9 and 0 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 31090-81:
(7*3)+(6*1)+(5*0)+(4*9)+(3*0)+(2*8)+(1*1)=80
80 % 10 = 0
So 31090-81-0 is a valid CAS Registry Number.

31090-81-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name p-methoxychalcone

1.2 Other means of identification

Product number -
Other names 6-methoxy-2-phenyl-4H-chromen-4-one

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:31090-81-0 SDS

31090-81-0Relevant academic research and scientific papers

Synthesis, phytotoxic, cytotoxic, acetylcholinesterase and butrylcholinesterase activities of N,N-diaryl unsymmetrically substituted thioureas

Begum, Saeedan,Choudhary, M. Iqbal,Khan, Khalid M.

experimental part, p. 1719 - 1730 (2010/05/18)

Fourteen N,N-diaryl unsymmetrically substituted thioureas were synthesised and their cytotoxic (in vitro), phytotoxic (in vitro), acetylcholinesterase and butrylcholinesterase activities were determined. Thiourea 16 exhibited high, and 1 and 3 showed significant phytotoxic activity. Thioureas 1, 3, 4, 6 and 10 showed significant activity and 2, 6 and 7 indicated moderate cytotoxic activities. Compound 12 exhibited butrylcholinesterase activity higher than a standard reference.

Microwave-assisted synthesis of N,N′-diaryl cyanoguanidines

Hamilton, Sean K.,Wilkinson, Doug E.,Hamilton, Gregory S.,Wu, Yong-Qian

, p. 2429 - 2431 (2007/10/03)

(Chemical Equation Presented) A mild, efficient, and high-yielding method for the synthesis of N,N′-diaryl cyanoguanidines from their corresponding thioureas under microwave-assisted conditions is described. A series of cyanoguanidines were synthesized containing both electron-donating and electron-withdrawing substituents. The reactions were facilitated by the use of polar solvents along with moderate temperatures.

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