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naphthalen-1-yl(phenyl)methanethione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33083-79-3

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33083-79-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33083-79-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,0,8 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 33083-79:
(7*3)+(6*3)+(5*0)+(4*8)+(3*3)+(2*7)+(1*9)=103
103 % 10 = 3
So 33083-79-3 is a valid CAS Registry Number.

33083-79-3SDS

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 naphthalen-1-yl(phenyl)methanethione

1.2 Other means of identification

Product number -
Other names Phenyl-1-naphthyl-thioketon

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:33083-79-3 SDS

33083-79-3Upstream product

33083-79-3Relevant academic research and scientific papers

-Annulation of Azaoxyallyl Cations and Thiocarbonyls for the Assembly of Thiazolidin-4-ones

Jaiswal, Vandana,Mondal, Biplab,Singh, Kuldeep,Das, Dinabandhu,Saha, Jaideep

supporting information, p. 5848 - 5852 (2019/08/26)

A base-promoted, efficient [3 + 2] annulation between azaoxyallyl cations and thiocarbonyls is reported for flexible access to highly functionalized thiazolidin-4-one derivatives in good to excellent yields. An intriguing feature of this method is the met

Gas-Solid Reactions: Photochemical Oxidation of Thioketones in the Crystalline State

Arjunan, P,Ramamurthy, V,Venkatesan, K

, p. 1765 - 1769 (2007/10/02)

Photochemical oxidation of 11 diaryl thioketones (1-11) was conducted in the solid state.Quite interestingly, of these only six were oxidized to the corresponding carbonyl compound whereas the rest were photostable.However, in solution all were readily oxidized.The difference in behaviour between the thioketones in the solid state has been rationalized on the basis of molecular arrangement in the crystal.X-ray crystal structure analyses of four thioketones were carried out in this connection.

THE CYCLOADDITION REACTIONS OF AROMATIC THIONES WITH MALEIC ANHYDRIDE, NORBORNENE, AND NORBORNADIENE

Ohmura, Haruo,Motoki, Shinichi

, p. 19 - 28 (2007/10/02)

The reactions of aryl 1-naphthyl thiones and aryl 2-naphthyl thiones with maleic anhydride, norbornene, and norbornadiene gave the 1,4-cycloadducts containing 3,4-dihydro-2H-thiopyran rings. 7H-Benzanthracene-7-thione also reacted with norbornene and

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