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18655-88-4

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18655-88-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18655-88-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,6,5 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18655-88:
(7*1)+(6*8)+(5*6)+(4*5)+(3*5)+(2*8)+(1*8)=144
144 % 10 = 4
So 18655-88-4 is a valid CAS Registry Number.

18655-88-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-dithia-4,5-dimethyl-4-cyclohexene

1.2 Other means of identification

Product number -
Other names 4,5-dimethyl-3H,6H-1,2-dithiin

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:18655-88-4 SDS

18655-88-4Downstream Products

18655-88-4Relevant articles and documents

An S-oxide of 6-tert-butyl-6-phenylpentathiane. Structure in the crystalline state and in solution and thermal decomposition

Ishii, Akihiko,Oshida, Hideaki,Nakayama, Juzo

, p. 3117 - 3119 (2007/10/03)

Oxidation of 6-tert-butyl-6-phenylpentathiane with trifluoroperacetic acid gave the pentathiane 3-oxide mainly as the monooxide. The 3-oxide takes a twist conformation both in the crystalline state and in solution. Thermal decomposition of the 3-oxide in the presence of 2,3-dimethyl-1,3-butadiene yielded both S2O- and S2-transferred products.

SYNTHESE ET REACTIVITE DE DITHIAPHOSPHADIGERMINANE ET -GERMINANE NOUVEAUX DITHIAPHOSPHONATES GERMANIES CYCLIQUES

Barrau, J.,Rima, G.,Satge, J.

, p. 99 - 106 (2007/10/03)

The synthesis of the six membered heterocycles (1) and (2) are described.Thermolysis of 1 generates the germylated heterocycles (3), (4), (5) and (AnPS2)3,4.These results are explained by a mechanism involving expulsion of and decomposition of the resulting transient thiadigermetane with formation of and .Exchange reactions between 1 and various chlorides are described.With metal 14 chlorides Σ2MCl2 the reactions lead to transient and metallathiones ; while with SCl2 the reaction leads to and singlet sulfur . - Key words: Germylated and phosphorylated heterocycles, transient species, germathione, singlet sulfur.

Diatomic Sulfur (S2)

Steliou, Kosta,Salama, Paul,Brodeur, Daniel,Gareau, Yves

, p. 926 - 927 (2007/10/02)

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