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pyridin-2-yl imidothiocarbamate dihydrobromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

99420-73-2

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99420-73-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99420-73-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,4,2 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 99420-73:
(7*9)+(6*9)+(5*4)+(4*2)+(3*0)+(2*7)+(1*3)=162
162 % 10 = 2
So 99420-73-2 is a valid CAS Registry Number.

99420-73-2SDS

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 pyridin-2-yl carbamimidothioate,dihydrobromide

1.2 Other means of identification

Product number -
Other names Pyridine-2,S-isothiuronium bromide hydrobromide

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:99420-73-2 SDS

99420-73-2Downstream Products

99420-73-2Relevant academic research and scientific papers

New Synthetic Routes to Unsymmetrical Diorganyl Sulfides

Deryagina,Korchevin,Papernaya

, p. 812 - 815 (2007/10/03)

A number of new methods for preparing unsymmetrical diorganyl sulfides was proposed. The methods rely on generation of thiolate anions from thiols, isothiuronium salts, and disulfides in the system hydrazine hydrate-KOH, followed by alkylation of the anions with alkyl halides. The hydrazine hydrate plays the role of medium and reducing agent, which prevents side thiol oxidation. The yield of sulfides reaches 98%. The reaction products are readily separated from the aqueous-hydrazine layer and purified by distillation. The yield of sulfides is reduced by a deficit of alkali and by increasing chain length and functionalization of alkyl groups in the alkyl halide. The reactivity of alkyl halides is independent of the nature of the halogen. From isothiuronium salts, 2-pyridyl sulfides were obtained in the highest yields.

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