14543-31-8 Usage
General Description
2,4-bis(allyloxy)-6-chloro-1,3,5-triazine is a chemical compound with the molecular formula C12H12ClN3O2. It is a chlorinated triazine derivative that is often used as a reactive intermediate in the synthesis of polymers and resins. 2,4-bis(allyloxy)-6-chloro-1,3,5-triazine is commonly employed as a crosslinking agent in the production of water-based coatings and adhesives. Its allyloxy groups make it suitable for use in various applications, including inks, textiles, and automotive coatings. Additionally, 2,4-bis(allyloxy)-6-chloro-1,3,5-triazine is considered to be a low-toxicity compound and does not present significant health hazards when handled according to proper safety practices.
Check Digit Verification of cas no
The CAS Registry Mumber 14543-31-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,5,4 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14543-31:
(7*1)+(6*4)+(5*5)+(4*4)+(3*3)+(2*3)+(1*1)=88
88 % 10 = 8
So 14543-31-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H10ClN3O2/c1-3-5-14-8-11-7(10)12-9(13-8)15-6-4-2/h3-4H,1-2,5-6H2
14543-31-8Relevant articles and documents
Preparation of Alkyl Ethers with Diallyltriazinedione-Type Alkylating Agents (ATTACKs-R) Under Acid Catalysis
Fujita, Hikaru,Yamashita, Rina,Fujii, Takanori,Yamada, Kohei,Kitamura, Masanori,Kunishima, Munetaka
, p. 4436 - 4446 (2019/07/03)
Diallyltriazinedione-type acid-catalyzed alkylating agents (ATTACKs-R) with 10 different alkyl groups (R), including benzyl, substituted benzyl, allyl, and methyl groups were synthesized. The palladium-catalyzed intramolecular O-to-N allylic rearrangement of 2,4-bis(allyloxy)-6-chloro-1,3,5-triazine was developed to introduce various alkoxy groups into the N,N′-dialkylated triazinedione skeleton. O-Alkylation of alcohols with ATTACKs-R was carried out in 1,4-dioxane in the presence of 2,6-di-tert-butylpyridinium trifluoromethanesulfonate or trifluoromethanesulfonic acid as a catalyst. Six selected ATTACKs-R bearing benzylic R groups were employed to prepare alkyl ethers from primary, secondary, and tertiary alcohols. The reactions of ATTACKs-R bearing an o-nitro-substituted benzyl group tended to afford low yields. Comparison of four different triazinedione-based benzylating reagents suggested that the N,N′-substituents affected the reactivity.
