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1-ALLYL-3,3-DIETHYL-2-THIOUREA, an allyl type thiourea, is an organosulfur compound that features a unique combination of sulfur and nitrogen atoms. It is recognized for its valuable properties as a cross-linking agent, which significantly contributes to the enhancement of material strength and durability in industrial applications.

21645-26-1

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21645-26-1 Usage

Uses

Used in Rubber and Plastics Industry:
1-ALLYL-3,3-DIETHYL-2-THIOUREA is used as a cross-linking agent for improving the strength and durability of rubber and plastic materials. Its ability to form links between polymer chains is crucial for the production of robust and long-lasting products in this industry.
Safety Note:
As with other chemicals, 1-ALLYL-3,3-DIETHYL-2-THIOUREA requires careful handling and exposure control to mitigate potential health risks, emphasizing the importance of proper safety measures during its use in industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 21645-26-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,6,4 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 21645-26:
(7*2)+(6*1)+(5*6)+(4*4)+(3*5)+(2*2)+(1*6)=91
91 % 10 = 1
So 21645-26-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H16N2S/c1-4-7-9-8(11)10(5-2)6-3/h4H,1,5-7H2,2-3H3,(H,9,11)

21645-26-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Allyl-3,3-diethyl-2-thiourea

1.2 Other means of identification

Product number -
Other names 1,1-diethyl-3-prop-2-enylthiourea

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:21645-26-1 SDS

21645-26-1Downstream Products

21645-26-1Relevant academic research and scientific papers

Synthesis of novel dithiocarbamates and xanthates using dialkyl azodicarboxylates: S–N bond formation

Ziyaei Halimehjani, Azim,Klepetá?ová, Blanka,Beier, Petr

, p. 1850 - 1858 (2018/03/06)

A one?pot three?component route for the synthesis of a novel category of dithiocarbamates or xanthates is developed by a reaction of in-situ generated dithiocarbamic acids or xanthates with dialkyl azodicarboxylates under mild and catalyst-free conditions. The reaction is characterized by a wide scope, high efficiency and straightforward isolation protocol. The synthetic utility of the dithiocarbamates and xanthates was demonstrated on the preparation of symmetrical and unsymmetrical thioureas, isothiocyanates, and thiocarbamates.

Photoinduced electron transfer reaction of tetraazathiapentalenes with trialkylamines

Hayashi, Hirokazu,Matsumura, Noboru,Mizuno, Kazuhiko

, p. 510 - 511 (2007/10/03)

The photoinduced electron transfer reaction of tetraazathiapentalenes with trialkylamines gives thiourea derivatives by dialkylamination of isothiocyanate derivatives, through radical anions of tetraazathiapentalenes and radical cations of trialkylamines.

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