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5857-39-6

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5857-39-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5857-39-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,5 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5857-39:
(6*5)+(5*8)+(4*5)+(3*7)+(2*3)+(1*9)=126
126 % 10 = 6
So 5857-39-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H3S.ClH.Hg/c1-2-4-5-3-1;;/h1-3H;1H;/q;;+1/p-1/rC4H3ClHgS/c5-6-4-2-1-3-7-4/h1-3H

5857-39-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name chloro(thiophen-2-yl)mercury

1.2 Other means of identification

Product number -
Other names Mercury,chloro-2-thienyl

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:5857-39-6 SDS

5857-39-6Relevant articles and documents

STUDIES OF HETEROCYCLIC COMPOUNDS. III. SYNTHESIS AND THERMAL DECOMPOSITIONS OF SOME 2-THIOPHENEMERCURIC DERIVATIVES

Obafemi, Craig A.

, p. 1 - 7 (1981)

2-Thiophenemercuric chloride(I), on reaction with sodium or silver thiocyanate, silver azide, silver acetate, and silver trifluoromethanesulfonate gave the 2-thiocyanate (2), 2-azide (4), 2-acetate (5) and 2-trifluoromethanesulfonate (6), respectively.The thermal decompositions of these compounds, together with that of 2,2'-dithienyl mercury, have been studied.The 2-thiophenemercuric triflate (6) decomposes at room temperature to give 2,2'-dithienylmercury.The 2-azide (4), when treated with either cyclohexene or triphenylphosphine, gave only the 2,2'-dithienylmercury.All the 2-thiophenemercuric salts decompose at about 300 deg C to give only a black insoluble residue.With the aid of some control experiments and comparison with previous work on phenyl- and p-tolyl-mercuric salts, a mechanism is proposed to account for the results.

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