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1-(2-hydroxyphenyl)-3-(4-nitrophenyl)thiourea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

107368-17-2

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107368-17-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107368-17-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,3,6 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 107368-17:
(8*1)+(7*0)+(6*7)+(5*3)+(4*6)+(3*8)+(2*1)+(1*7)=122
122 % 10 = 2
So 107368-17-2 is a valid CAS Registry Number.

107368-17-2Relevant academic research and scientific papers

Potassium Periodate Mediated Oxidative Cyclodesulfurization toward Benzofused Nitrogen Heterocycles

Duangkamol, Chuthamat,Pattarawarapan, Mookda,Phakhodee, Wong

, p. 1981 - 1990 (2020/07/03)

A convenient oxidative cyclodesulfurization method toward the synthesis of benzofused nitrogen heterocycles using inexpensive and readily available potassium periodate as an oxidant was developed. Upon treating isothiocyanates with ortho -substituted anilines bearing N, N -, N, O -, and N, S -bis-nucleophiles, followed by an intramolecular cyclization of the in situ generated monothioureas, substituted 2-aminobenzazole series were rapidly accessible in good to excellent yields. The protocol can accommodate various substituents on both substrates while allowing more efficient, greener, and operational simpler process relative to other oxidative coupling reactions. Tetracyclic quinazolinone derivatives were also afforded in high yields in a single preparative step and chromatography-free.

One-pot reaction for the synthesis of N-substituted 2-aminobenzoxazoles using triphenylbismuth dichloride as cyclodesulfurization reagent

Murata, Yuki,Matsumoto, Natsuho,Miyata, Maya,Kitamura, Yuki,Kakusawa, Naoki,Matsumura, Mio,Yasuike, Shuji

, p. 18 - 23 (2018/02/09)

The treatment of various 2-aminophenols with isothiocyanates afforded thioureas, which were reacted in situ with triphenylbismuth dichloride in the presence of triethylamine to give the expected N-substituted benzoxazol-2-amines in good to excellent yields. Triphenylbismuth dichloride promoted the successful cyclodesulfurization of thioureas with short reaction times under mild reaction conditions. This reaction is the first example of the synthesis of heterocyclic rings using a pentavalent organobismuth reagent.

Ultrasound-assisted synthesis of substituted 2-aminobenzimidazoles, 2-aminobenzoxazoles, and related heterocycles

Phakhodee, Wong,Duangkamol, Chuthamat,Wiriya, Nittaya,Pattarawarapan, Mookda

supporting information, p. 5290 - 5293 (2016/11/11)

A sonochemical method for the synthesis of 2-aminobenzimidazoles and 2-aminobenzoxazoles, as well as chiral aminooxazolines and a chiral substituted quinazolin-5-one is reported. Using the Ph3P–I2system in the presence of triethylami

Highly efficient one-pot synthesis of 2-aminobenzoxazoles using triflic acid as a cyclodesulfurizing reagent

Khatik, Gopal L.,Dube, Namita,Pal, Anang,Nair, Vipin A.

experimental part, p. 2631 - 2639 (2011/08/07)

An efficient one-pot synthetic strategy for 2-aminobenzoxazoles was developed from isothiocyanates and 2-aminophenol using triflic acid as a cyclodesulfurizing reagent. Taylor & Francis Group, LLC.

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