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5-(decylsulfanyl)-1,3,4-thiadiazole-2(3H)-thione is a chemical compound with the molecular formula C11H19N2S3. It is a derivative of 1,3,4-thiadiazole, a heterocyclic compound containing sulfur and nitrogen atoms. The molecule features a decylsulfanyl group (a sulfur atom bonded to a decyl chain) attached to the 5-position of the thiadiazole ring, and a thione group (a sulfur atom double-bonded to a carbon atom) at the 2-position. 5-(decylsulfanyl)-1,3,4-thiadiazole-2(3H)-thione may have potential applications in various chemical and pharmaceutical industries due to its unique structure and properties.

4858-30-4

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4858-30-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4858-30-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,5 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4858-30:
(6*4)+(5*8)+(4*5)+(3*8)+(2*3)+(1*0)=114
114 % 10 = 4
So 4858-30-4 is a valid CAS Registry Number.

4858-30-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-decylsulfanyl-3H-1,3,4-thiadiazole-2-thione

1.2 Other means of identification

Product number -
Other names 5-(decylthio)-1,3,4-thiadiazole-2-thiol

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:4858-30-4 SDS

4858-30-4Downstream Products

4858-30-4Relevant academic research and scientific papers

Metal-free and green synthesis of a series of new bis(2-alkylsulfanyl-[1,3,4]thiadiazolyl)-5,5′-disulfides and 2,2′-Dibenzothiazyl disulfide via oxidative self-coupling using hydrogen peroxide

Ching Juan, Joon,Ghaffari Khaligh, Nader,Heidelberg, Thorsten,Ling Ong, Chiu

, (2021/12/29)

Many disulfide and 1,3,4-thiadiazole-1,2-dithiol compounds have been extensively investigated in the pharmaceutical industry due to their unique biological properties. A series of new bis(2-alkylsulfanyl-[1,3,4]thiadiazolyl)-5,5′-disulfide derivatives containing two 1,3,4-thiadiazole rings linked by S[sbnd]S bond spacer were synthesized via the oxidative self-coupling of 5-alkylsulfanyl-[1,3,4]thiadiazole-2-thiol using hydrogen peroxide and ethanol as green oxidant and solvent, respectively. The excellent yields of 93–97% with 100% conversion were achieved with a simple one-pot synthesis. There is no over-oxidation of 5-alkylsulfanyl-[1,3,4]thiadiazole-2-thiol and 2-mercaptobenzothiadiazole that leads to the formation of by-products such as thiosulfinate, thiosulfonate, and sulfonic acid. In this process, a straightforward, short reaction time, metal-free, reusable solvent, and mild reaction conditions are applied to produce bis(2-alkylsulfanyl-[1,3,4]thiadiazolyl)-5,5′-disulfides and 2,2′-dibenzothiazyl disulfide. Therefore, the oxidative self-coupling is potential for other disulfide compounds.

Synthesis of poly(glycerol-succinic acid)-dithiocarbamate and poly(glycerol-succinic acid)-1,3,4-thiadiazole dendrimers and their use as anti-wear oil additives

Kim, Yeong-Joon,Hoang, Quoc-Viet,Kim, Sung-Ki,Cho, Chang-Yong,Kim, Jeongkwon,Chung, Keun-Woo,Kim, Young-Wun

, p. 2044 - 2050 (2013/09/02)

A series of poly(glycerol-succinic acid) dithiocarbamate and 1,3,4-thiadiazole dendrimers, which have potential as anti-wear oil additives, were synthesized. Their anti-wear properties in three different oils (100N, DB-51, and soybean) were evaluated usin

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