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1-Benzoyl-3-(2-naphtyl)thiourea is an organic compound with the chemical formula C18H13N3OS. It is a derivative of thiourea, featuring a benzoyl group attached to the nitrogen atom and a 2-naphtyl group attached to the other nitrogen atom. This white crystalline solid is known for its potential applications in the synthesis of various chemical compounds and as an intermediate in the preparation of pharmaceuticals and agrochemicals. The compound is characterized by its melting point, which is around 195-198°C, and is typically used in research and development settings due to its reactivity and structural properties.

4921-85-1

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4921-85-1 Usage

Compound class

Thioureas

Common uses

Catalyst for the synthesis of various organic compounds, reagent in chemical research

Physical appearance

White crystalline solid

Molar mass

342.41 g/mol

Versatility

Potential applications in pharmaceuticals, agrochemicals, and materials science

Biological properties

Antimicrobial and anticancer properties

Potential use

Promising candidate for drug development

Precautions

Potential health hazards and environmental impact when handling BNTU

Check Digit Verification of cas no

The CAS Registry Mumber 4921-85-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,2 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4921-85:
(6*4)+(5*9)+(4*2)+(3*1)+(2*8)+(1*5)=101
101 % 10 = 1
So 4921-85-1 is a valid CAS Registry Number.
InChI:InChI=1/C18H14N2OS/c21-17(14-7-2-1-3-8-14)20-18(22)19-16-11-10-13-6-4-5-9-15(13)12-16/h1-12H,(H2,19,20,21,22)

4921-85-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Benzoyl-1-(β-naphthyl)-2-thiourea

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4921-85-1 SDS

4921-85-1Downstream Products

4921-85-1Relevant academic research and scientific papers

Synergism of fused bicyclic 2-aminothiazolyl compounds with polymyxin B against: Klebsiella pneumoniae

Wang, Rong,Hou, Shuang,Dong, Xiaojing,Chen, Daijie,Shao, Lei,Qian, Liujia,Li, Zhong,Xu, Xiaoyong

supporting information, p. 2060 - 2066 (2017/11/22)

A series of fused bicyclic 2-aminothiazolyl compounds were synthesized and evaluated for their synergistic effects with polymyxin B (PB) against Klebsiella pneumoniae (SIPI-KPN-1712). Some of the synthesized compounds exhibited synergistic activity. When 4 μg ml-1 compound B1 was combined with PB, it showed potent antibacterial activity, achieving 64-fold reduction of the MIC of PB. Furthermore, compound B1 showed prominent synergistic efficacy in both concentration gradient and time-kill curves in vitro. In addition, B1 combined with PB also exhibited synergistic and partial synergistic effect against E. coli (ATCC25922 and its clinical isolates), Acinetobacter baumannii (ATCC19606 and its clinical isolates), and Pseudomonas aeruginosa (Pae-1399).

Microwave Promoted Efficient Synthesis of N-Aryl-N′-aroyl Thioureas under Solvent-Free and Phase Transfer Catalysis Conditions

Wei, Tai-Bao,Lin, Qi,Zhang, You-Ming,Wei, Wei

, p. 181 - 186 (2007/10/03)

A simple, rapid and efficient method for the synthesis of N-aryl-N′-aroyl thioureas under phase transfer catalysis, microwave irradiation and solvent-free conditions is reported.

A mild and efficient synthesis of N-aryl-N′-aroyl thioureas under phase transfer catalysis and solvent-free conditions

Wei, Tai-Bao,Lin, Qi,Zhang, You-Ming,Wei, Wei

, p. 666 - 667 (2007/10/03)

A series of N-aryl-N′-aroyl thioureas 3a-m were synthesized in high yields (80.0-98.1%) by an environmentally benign, simple and efficient method under phase transfer catalysis and solvent-free conditions.

Thermal Decomposition of Aromatic Thioureas

Parkanyi, Cyril,Al-Salamah, Mohammed A.

, p. 101 - 104 (2007/10/02)

Thermal decomposition of aromatic and heteroaromatic thioureas in boiling chlorobenzene is a first-order reaction.The reaction involves intramolecular hydrogen transfer followed by a cleavage of the C - N bond which is the rate-limiting step.The rate constants of decomposition have been determined and correlated with quantum-chemical reactivity indices. - Key words: Thioureas, Isothiocyanates, Thermal Decomposition, Side-Chain Elimination, Kinetics

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