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15863-19-1

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15863-19-1 Usage

Type of compound

thiourea derivative

Common uses

reagent in organic chemistry reactions

Potential biological activities

antitumor, antiviral

Potential pharmacological activities

not mentioned

Other potential uses

ligand for metal ion coordination, synthesis of heterocyclic compounds with biological activities

Versatility

has a range of potential applications in both chemical and biological research

Check Digit Verification of cas no

The CAS Registry Mumber 15863-19-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,6 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 15863-19:
(7*1)+(6*5)+(5*8)+(4*6)+(3*3)+(2*1)+(1*9)=121
121 % 10 = 1
So 15863-19-1 is a valid CAS Registry Number.

15863-19-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-cyclohexyl-3-(4-methylphenyl)thiourea

1.2 Other means of identification

Product number -
Other names 1-cyclohexyl-3-p-tolyl-thiourea

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:15863-19-1 SDS

15863-19-1Relevant articles and documents

Synthesis and Reactivity of NNNNN-Pincer Multidentate Pyrrolyl Rare-Earth-Metal Amido-Chloride or Dialkyl Complexes

Cui, Peng,Du, Jun,Huang, Zeming,Sheng, Weiming,Wang, Shaowu,Wei, Yun,Xu, Xiaolong,Zhang, Lijun,Zhang, Xiuli,Zhou, Shuangliu,Zhu, Xiancui

supporting information, p. 4525 - 4534 (2020/12/22)

The NNNNN-pincer multidentate pyrrolyl rare-earth-metal amido-chloride complexes {η1:κ3-2,5-[CH3N(CH2CH2)2NCH2]2C4H2N}RECl[N(SiMe3)2] (RE = Y (2a), Sm (2b), Dy (2c), Er (2d), Yb (2e)) were synthesized by one step from reactions of [(Me3Si)2N]3RE(μ-Cl)Li(T

One-Pot Synthesis of C2 Symmetric and Asymmetric N,N′,N″-Substituted Guanidines from Aryl Isothiocyanates and Amines

Wangngae, Sirilak,Pattarawarapan, Mookda,Phakhodee, Wong

, p. 1121 - 1127 (2016/05/19)

Highly substituted guanidines were conveniently prepared through a one-pot reaction between aryl isothiocyanates and amines mediated by the Ph3P-I2/Et3N system. The C 2-symmetric N,N′,N″-substituted guanidines were readily accessed using a 1:2 molar ratio of an aryl isothiocyanate and an amine; while sequential addition of two different amines in equimolar ratios gave rise to asymmetric derivatives. Both primary and secondary amines were found to react preferentially with electron-deficient aryl isothiocyanates, rapidly providing guanidines in good yields under mild conditions.

The synthesis of some new sulfur-bearing various heterocyclic systems derived from asymmetrical N,N′-disubstituted thiourea derivatives

Saad, Hosam

, p. 1557 - 1567 (2007/10/03)

The heterocyclization of an asymmetrical N,N′-disubstituted thiourea (1a-d) in ring closure reactions with Br2/AcOH, ethyl chloroacetate, diethyl oxalate, diethyl malonate, and hydrazine hydrate led to the direct formation of sulfur-bearing var

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