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30863-82-2

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30863-82-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30863-82-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,8,6 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 30863-82:
(7*3)+(6*0)+(5*8)+(4*6)+(3*3)+(2*8)+(1*2)=112
112 % 10 = 2
So 30863-82-2 is a valid CAS Registry Number.

30863-82-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-tris(phenylsulfanyl)-1,3,5-triazine

1.2 Other means of identification

Product number -
Other names triphenyltrithiocyanurate

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:30863-82-2 SDS

30863-82-2Relevant articles and documents

Pd/PTABS: Low-Temperature Thioetherification of Chloro(hetero)arenes

Bandaru, Siva Sankar Murthy,Bhilare, Shatrughn,Cardozo, Jesvita,Chrysochos, Nicolas,Schulzke, Carola,Sanghvi, Yogesh S.,Gunturu, Krishna Chaitanya,Kapdi, Anant R.

, p. 8921 - 8940 (2019/07/08)

The thioetherification of heteroaryl chlorides is an essential synthetic methodology that provides access to bioactive drugs and agrochemicals. Due to their (actual or potential) industrial importance, the development of efficient and low-temperature protocols for accessing these compounds is a requirement for economic and ecologic reasons. A particular highly effective catalytic protocol using the Pd/PTABS system at only 50 °C was developed accordingly. The coupling between chloroheteroarenes and a variety of less reactive arylthiols and alkylthiols was carried out with a high efficiency. Heteroarenes of commercial relevance such as purines and pyrimidines were also found to be useful substrates for the reported transformation. The commercial drug Imuran (azathioprine) was synthesized as an example, and its preparation could be optimized. DFT studies were performed to understand the electronic effects of the tested ligands on the catalytic reaction.

Janus head type lone pair-π-lone pair and S?F?S interactions in retaining hexafluorobenzene

Mehrotra, Sonam,Angamuthu, Raja

, p. 4438 - 4444 (2016/07/06)

A series of eight tris-arylthiotriazines were synthesized to study the lone pair-π interaction between the triazine ring centroid of these molecules and halogenated solvents. All the eight compounds were characterized using 1H and 13C NMR spectroscopy and single crystal X-ray diffraction techniques. All these compounds show interesting structural properties in the solid state. Unprecedented Janus head type lp?π?lp and S?F?S interactions were observed between one of the tris-arylthiotriazines and hexafluorobenzene.

THE OXIDATION OF TRITHIOCYANURIC ACID AND OF ITS N- AND S-ESTERS

Tripolt, Robert,Nachbaur, Edgar

, p. 173 - 176 (2007/10/02)

The reaction of trithiocyanuric acid 1 with 3 equivalents of 2-benzenesulfonyl-3-phenyl-oxaziridine affords the highly reactive 1,3,5-triazine-2,4,6-trisulfenic acid 3, which is trapped by reaction with diazomethane to give the trimethylester of 3.Additionally the reactions of trithioisocyanurates and trithiocyanurates with meta-chloroperbenzoic acid (mCPBA), oxaziridine, dimethyldioxirane and chlorine are studied.

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