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85609-04-7

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85609-04-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85609-04-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,6,0 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 85609-04:
(7*8)+(6*5)+(5*6)+(4*0)+(3*9)+(2*0)+(1*4)=147
147 % 10 = 7
So 85609-04-7 is a valid CAS Registry Number.

85609-04-7SDS

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-bis(ethylthio)benzene

1.2 Other means of identification

Product number -
Other names 1,2-Bis-aethylmercapto-benzol

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:85609-04-7 SDS

85609-04-7Relevant articles and documents

A method for preparing phthalic of the dithiol

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Paragraph 0035-0043, (2020/05/05)

The invention provides a method for preparing benzene-1,2-dithiol. The method includes the steps that metal sodium, ethyl mercaptan and 1,2-dichlorobenzene serve as starting raw materials, two halogen atoms of the 1,2-dichlorobenzene are completely substituted in polar solvents N,N-dimethyl formamide by controlling the molecular proportion of the reactants through the high nucleophilic substitution capacity of sodium thioethylate, 1,2-2 ethyl petrol phenyl sulfide is obtained with the high yield, then sulphur atom deprotection is carried out under the reducing action of the metal sodium and naphthalene, and the target product benzene-1,2-dithiol is produced in an almost-quantitative mode after acidizing is carried out through hydrochloric acid. The preparing method is simple, convenient to operate, low in price and high in yield, and has the broad application prospects in the fine chemical engineering and the pharmaceutical industry.

BROMINATION OF 2,3-UNSATURATED 1,4-DISULFIDES

Mursakulov, I. G.,Ramazanov, E. A.,Kerimov, F. F.,Abbasov, I. M.,Zefirov, N. S.

, p. 113 - 116 (2007/10/02)

The bromination of 1,2-bis(alkylthio)-1-cyclohexenes, unsubstituted and substituted 2,3-tetramethylene-5,6-dihydro-1,4-dithiins, and 2,3-tetramethylene-5,6-dihydro-1,4-oxathiins is accompanied by spontaneous dehydrobromination with the formation of the pr

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