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Carbamodithioic acid, cyclohexyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22292-07-5

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22292-07-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22292-07-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,2,9 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 22292-07:
(7*2)+(6*2)+(5*2)+(4*9)+(3*2)+(2*0)+(1*7)=85
85 % 10 = 5
So 22292-07-5 is a valid CAS Registry Number.

22292-07-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclohexylcarbamodithioic acid

1.2 Other means of identification

Product number -
Other names N-cyclohexyldithiocarbamic acid

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:22292-07-5 SDS

22292-07-5Relevant academic research and scientific papers

Synthesis, characterization, semi-empirical study, and biological activities of organotin(IV) complexes with cyclohexylcarbamodithioic acid as biological active ligand

Jabbar, Saba,Shahzadi, Iram,Rehman, Rafia,Iqbal, Humaira,Qurat-Ul-Ain,Jamil, Aneela,Kousar, Rubina,Ali, Saqib,Shahzadi, Saira,Choudhary, Muhammad Aziz,Shahid, Muhammad,Khan, Qaiser Mehmood,Sharma, Saroj K.,Qanungo, Kushal

, p. 572 - 590 (2012)

Cyclohexylcarbamodithioic acid has been synthesized by the reaction of cyclohexylamine with carbon disulfide at room temperature. Its complexes have been synthesized by the reaction of cyclohexylcarbamodithioic acid with organotin(IV) chlorides in 1 : 1/1

Multiple-structured nanocrystals towards bifunctional photoluminescent- superhydrophobic surfaces

Hou, Linrui,Wang, Caifeng,Chen, Li,Chen, Su

, p. 3863 - 3868 (2010)

We report a simple and efficient strategy for the preparation of diverse hierarchical structures of dithiocarbamate-functionalized CdS nanocrystals (NCs) exhibiting both photoluminescent and hydrophobic properties via a facile interfacial self-assembly te

Cobalt mediated by desulfurization toward the synthesis of isothiocyanates

Seelam, Mohan,Shaik, Bajivali,Kammela, Prasada Rao

supporting information, p. 1759 - 1765 (2016/10/31)

A highly efficient and simple protocol for the construction of aromatic and aliphatic isothiocyanates from their respective amines in the presence of cheap, readily available, and air-stable cobalt catalyst is described. All reactions were carried out under optimized reaction conditions and gave target products in good to excellent yields within shorter reaction time.

Synthesis, antifungal activities and molecular docking studies of novel 2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl)propyl dithiocarbamates

Zou, Yan,Yu, Shichong,Li, Renwu,Zhao, Qingjie,Li, Xiang,Wu, Maocheng,Huang, Ting,Chai, Xiaoxun,Hu, Honggang,Wu, Qiuye

, p. 366 - 374 (2014/02/14)

A series of 2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl) propyl dithiocarbamates as new analogs of fluconazole were synthesized and their antifungal activities were evaluated. Among these compounds, 2a-f and 3a-q exhibited higher activities than fluconazole against nearly all fungi tested except Aspergillus fumigatus. Noticeably, the in vitro biological activities of 2b, 3a, 3c, 3h-k, and 3o-q against Candida species were much better than those of fluconazole and ketoconazole. Also, 2a-d, 3a-d, 3e-f, 3h-k, 3p and 3q showed higher activities against A. fumi than fluconazole. Computational docking experiments indicated that the inhibition of CYP51 involved a coordination bond with iron of the heme group, the hydrophilic H-bonding region, the hydrophobic region, and the narrow hydrophobic cleft.

In situ formation of thermally stable, room-temperature ionic liquids from CS2 and amidine/amine mixtures

Yu, Tao,Yamada, Taisuke,Weiss, Richard G.

experimental part, p. 5492 - 5499 (2011/12/14)

Amidinium dithiocarbamates salts with diverse structures are prepared in situ by adding one equivalent of CS2 to an equimolar mixture of two nonionic molecules, an amidine and an amine. Many of the salts made in this way are room temperature ionic liquids (RTILs) and the others (ILs) melt well below the decomposition temperature of the salts, ca. 80 °C. Unlike the analogous amidinium carbamate RTILs, which are made by adding CO2 to amidine/amine mixtures and decompose near 50 °C, the amidinium dithiocarbamates do not revert to their amidine/amine mixtures when they are heated. The thermal, rheological, conductance, and spectroscopic properties of representative examples from a total of 50 of these ILs and RTILs are reported, comparisons between them and their nonionic phases (as well as with their amidinium carbamates analogues) are made, and the thermolysis pathways of the ammonium dithiocarbamates are investigated.

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