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20962-92-9

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20962-92-9 Usage

Chemical Properties

Light Yellow Oil

Uses

Phenothiazine (P318040) derivative.

Check Digit Verification of cas no

The CAS Registry Mumber 20962-92-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,9,6 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 20962-92:
(7*2)+(6*0)+(5*9)+(4*6)+(3*2)+(2*9)+(1*2)=109
109 % 10 = 9
So 20962-92-9 is a valid CAS Registry Number.

20962-92-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 10-prop-2-enylphenothiazine

1.2 Other means of identification

Product number -
Other names N-allylphenothiazine

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:20962-92-9 SDS

20962-92-9Relevant articles and documents

Monomeric and polymeric phenothiazine photosensitizers for photoinitiated cationic polymerization

Gomurashvili, Zaza,Crivello, James V.

, p. 2962 - 2969 (2002)

The syntheses of several phenothiazine compounds bearing cationically polymerizable vinyl, vinyl ether and epoxide groups are described. These monomers were rapidly and efficiently polymerized or copolymerized by UV irradiation in the presence of onium salt photoinitiators. In addition, the monomers simultaneously function as efficient photosensitizers for the photolysis of the onium salts. In this article, the use of these polymerizable photosensitizers for the photopolymerizations of epoxide and vinyl ether monomers is reported. The inclusion of a small amount of the monomeric photosensitizer is effective in markedly accelerating the cationic photopolymerization of the bulk monomer. Polymers prepared by the polymerization of the monomeric phenothiazine photosensitizers also exhibit excellent photosensitization activity when used in combination with diaryliodonium, triarylsulfonium, and dialkylphenacylsulfonium salt photoinitiators.

Platinum-catalyzed allylation of aminonaphthalenes with allylic acetates

Yang, Shyh-Chyun,Feng, Wei-Hao,Gan, Kim-Hong

, p. 3752 - 3760 (2007/10/03)

The activation of C-O bonds in allylic acetates has been accelerated by carrying out the reactions in the presence of platinum complexes associated with ligands. Platinum-catalyzed allylation of aminonaphthalenes with allylic acetates leads to N-allylic aminonaphthalenes in good yields.

One-pot synthesis of pharmacologically active diamines via rhodium- catalysed carbonylative hydroaminomethylation of heterocyclic allylic amines

Rische, Thorsten,Mueller, Kai-Sven,Eilbracht, Peter

, p. 9801 - 9816 (2007/10/03)

Pharmacologically active derivatives of phenothiazine, iminodibenzyl, carbazole and pyrazole are prepared with high yields and chemoselectivity by the reaction of the corresponding N-allylic or N-methallylic compounds, primary or secondary amines, carbon monoxide and hydrogen in the presence of [Rh(cod)Cl]2 as catalyst via a one pot hydroformylation - amine condensation - reduction sequence.

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