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1,3,5-Triazine-2(1H)-thione,tetrahydro-5-(1-methylethyl)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23510-30-7

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23510-30-7 Usage

Chemical class

Organic compound

Subclass

Triazines

Sulfur-containing

Yes

Heterocyclic compound

Yes

Application

Rubber accelerator and vulcanizing agent

Purpose

Improves mechanical and chemical properties of rubber

Effectiveness

Increases tensile strength and abrasion resistance of rubber materials

Usage in production

Medical gloves, automotive products, and industrial rubber goods

Performance enhancement

Enhances performance and durability of rubber materials

Check Digit Verification of cas no

The CAS Registry Mumber 23510-30-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,5,1 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 23510-30:
(7*2)+(6*3)+(5*5)+(4*1)+(3*0)+(2*3)+(1*0)=67
67 % 10 = 7
So 23510-30-7 is a valid CAS Registry Number.

23510-30-7SDS

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 5-isopropyl-1,3,5-triazinane-2-thione

1.2 Other means of identification

Product number -
Other names 1-Isopropyl-hexahydrotriazinthion-4

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:23510-30-7 SDS

23510-30-7Downstream Products

23510-30-7Relevant academic research and scientific papers

Straightforward Three-Component Synthesis of N′,N′′-Disubstituted N -Alkyl-1,3,5-Triazinanes

Bunev, Alexander S.,Frontera, Antonio,Grigoriev, Mikhail S.,Grudova, Mariya V.,Kletskov, Alexey V.,Presnukhina, Sofia,Shetnev, Anton,Sinelshchikova, Anna A.,Zaytsev, Vladimir P.,Zubkov, Fedor I.

supporting information, p. 1067 - 1072 (2020/07/04)

Efficient approaches towards the synthesis of various N-substituted 1,3,5-triazinanes based on a transformation of N -alkyl-1,5,3-dioxazepanes or on a domino reaction involving condensation of various amines, amides, and paraformaldehyde are described for the first time. Mg(ClO 4) 2 was shown to be one of the most potent additives for the condensation. The proposed approaches permit the synthesis of a broad spectrum of substituted sym -triazinanes in good yields with relatively easy workup. In the case of the multicomponent reaction, the approach allows the preparation of the target substances from simple and easily accessible reagents. The representatives of the resulting compounds were found to possess no antimicrobial or cytotoxic activity in in vitro bioassays.

Catalytic cycloaminomethylation of ureas and thioureas with N,N-bis(methoxymethyl)alkanamines

Khairullina,Geniyatova,Meshcheryakova,Khalilov,Ibragimov,Dzhemilev

, p. 116 - 120 (2015/03/04)

An efficient procedure has been developed for the synthesis of 5-alkyl-1,3,5-triazinan-2-ones, 5-alkyl-1,3,5-triazinane-2-thiones, and 2,6-dialkylhexahydro-2,3a,4a,6,7a,8a-hexaazacyclopenta[def]fluorene-4,8(1H,5H)-diones by reactions of urea, thiourea, an

Synthesis of 5-alkyl-1,3,5-triazinan-2-ones and 5-alkyl-1,3,5-triazinane-2- thiones using Cu- and Sm-containing catalysts

Khairullina,Geniyatova,Ibragimov,Dzhemilev

, p. 904 - 908 (2013/07/26)

Efficient procedures have been developed for the synthesis of 5-alkyl-1,3,5-triazinan-2-ones and 5-alkyl-1,3,5-triazinane-2-thiones by reaction of urea (thiourea) with primary alkylamines and N,N,N′,N′- tetramethylmethylenediamine and by reaction of prima

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