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21645-26-1

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21645-26-1 Usage

General Description

1-Allyl-3,3-diethyl-2-thiourea is a chemical compound that is characterized as an allyl type thiourea. Thioureas are a group of organosulfur compounds that contain sulfur and nitrogen atoms. The substance is primarily used in industrial applications, particularly in the manufacturing of rubber and plastics, due to its excellent properties as a cross-linking agent. Its ability to form links between polymer chains can help to improve the strength and durability of these materials. Like other chemicals, handling and exposure require proper safety measures due to potential health risks.

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 articles and documents

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.

Form of transport of isothiocyanates, stability and cleavability. 3. On therapy with isothiocyanate groups.

SCHULTZ,GLEIXNER

, p. 879 - 894 (2007/10/04)

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