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16738-19-5

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16738-19-5 Usage

General Description

(2,5-xylyl)thiourea is a chemical compound with the molecular formula C9H12N2S. It is a derivative of thiourea, a sulfur-containing compound, and is formed by the substitution of two hydrogen atoms in thiourea with a 2,5-xylyl group. (2,5-xylyl)thiourea is used in various industries such as the rubber and agricultural sectors, where it acts as a vulcanization accelerator and a fungicide, respectively. (2,5-xylyl)thiourea has also been studied for its potential applications in the field of medicine, particularly in the treatment of certain types of cancer. It is important to handle this compound with caution as it is considered to be potentially harmful if ingested or inhaled, and can cause irritation to the skin and eyes upon contact.

Check Digit Verification of cas no

The CAS Registry Mumber 16738-19-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,3 and 8 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 16738-19:
(7*1)+(6*6)+(5*7)+(4*3)+(3*8)+(2*1)+(1*9)=125
125 % 10 = 5
So 16738-19-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H12N2S/c1-6-3-4-7(2)8(5-6)11-9(10)12/h3-5H,1-2H3,(H3,10,11,12)

16738-19-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,5-dimethylphenyl)thiourea

1.2 Other means of identification

Product number -
Other names Urea,2-thio-1-(2,5-xylyl)

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:16738-19-5 SDS

16738-19-5Relevant articles and documents

Design, synthesis and biological evaluation of novel semicarbazone-selenochroman-4-ones hybrids as potent antifungal agents

Xu, Hang,Su, Xin,Liu, Xiao-qian,Zhang, Kai-peng,Hou, Zhuang,Guo, Chun

supporting information, (2019/10/19)

A series of novel 2,3-dihydro-4H-1-benzoselenin-4-one (thio)semicarbazone derivatives were designed and synthesized by using molecular hybridization approach. All the target compounds were characterized by HRMS and NMR and evaluated in vitro antifungal activity against five pathogenic strains. In comparison with precursor selenochroman-4-ones, the hybrid molecules in this study showed significant improvement in antifungal activities. Notably, compound B8 showed significant antifungal activity against other strains excluding Aspergillus fumigatus (0.25 μg/mL on Candida albicans, 2 μg/mL on Cryptococcus neoformans, 8 μg/mL on Candida zeylanoides and 2 μg/mL on fluconazole-sensitive strains of Candida albicans). Moreover, compounds B8, B9 and C2 also displayed most potent activities against four fluconazole-resistance strains. Especially the MIC values of the hybrid molecule B8 against fluconazole-resistant strains were in the range of 0.5–2 μg/mL. Therefore, the molecular hybridization approach in this study provided new ideas for the development of antifungal drug.

Synthesis and biological activities of new 1,4-benzothiazine derivatives

Kajino,Mizuno,Tawada,Shibouta,Nishikawa,Meguro

, p. 2888 - 2895 (2007/10/02)

New 2H-1,4-benzothiazin-3(4H)-one derivatives possessing (4-phenyl-1-piperazinyl)alkyl moieties at the 2-position were synthesized and tested for calcium antagonistic and calmodulin antagonistic activities. Antihypertensive effects in spontaneously hypertensive rats were also evaluated. In general, these compounds were rather weak calcium channel blockers, although, in contrast, many of them had moderate to potent calmodulin antagonistic activity, and 2-[3-(4-(4-fluorophenyl)-1-piperazinyl]propyl]-2H-1,4-benzothiazin-3(4H )-one derivatives 45, 74 and 75 showed potent antihypertensive effects.

Attempts of sulfonylthiourea synthesis. 1. Reactions between sulfonamides and thioureas or rhodanides and isothiocyanates

Karba

, p. 844 - 848 (2007/10/05)

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