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3-BroMopyridine-2-thiol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65938-86-5

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65938-86-5 Usage

Uses

3-Bromo-2-pyridinethiol is a reactant in the synthesis of -aryl-3-sulfonamide derivatives.

Check Digit Verification of cas no

The CAS Registry Mumber 65938-86-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,9,3 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 65938-86:
(7*6)+(6*5)+(5*9)+(4*3)+(3*8)+(2*8)+(1*6)=175
175 % 10 = 5
So 65938-86-5 is a valid CAS Registry Number.

65938-86-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-bromo-1H-pyridine-2-thione

1.2 Other means of identification

Product number -
Other names 2-Mercapto-3-brom-pyridin

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:65938-86-5 SDS

65938-86-5Upstream product

65938-86-5Downstream Products

65938-86-5Relevant academic research and scientific papers

Grignard-Reagent-Promoted Desulfonylation/Intramolecular Coupling for the Synthesis of 2-(1-Fluorovinyl)pyridines

Jiang, Gaoxi,Kang, Lei,Qian, Jinlong,Yang, Huameng,Zhang, Jinlong

supporting information, p. 9118 - 9122 (2020/12/02)

A novel process involving Grignard-reagent-promoted desulfonylation/intramolecular coupling of readily available α-fluoro-α,β-unsaturated-(2-pyridyl)sulfones was realized that provided a series of polysubstituted 2-(1-fluorovinyl)pyridines in good yields. The intrinsic coordination between pyridine and Mg(II) along with the "negative fluorine effect"of the substrates should play the key role for the smooth transformation in the absence of transition-metal catalysts.

Synthesis and characterization of 2-pyridylsulfur pentafluorides

Kanishchev, Oleksandr S.,Dolbier, William R.

supporting information, p. 280 - 284 (2015/04/21)

Current approaches to prepare SF5-substituted heterocycles during the synthesis of targeted heterocyclic compounds require the use of SF5-functionalized aryl or alkyne reagents or SF5Cl as a source of the SF5 functional group. Herein we report that excess oxidative fluorination of 2,2' -dipyridyl disulfide with a KF/Cl2 /MeCN system leads to the formation of thirteen new 2-pyridylsulfur chlorotetrafluorides (2-SF4Cl-pyridines). These molecules are found to undergo further chlorine-fluorine exchange reactions by treatment with silver(I) fluoride enabling ready access to a series of ten new substituted 2-pyridylsulfur pentafluorides (2-SF5-pyridines). This is the first preparatively simple and readily scalable example of the transformation of an existing heterocyclic sulfur functionality to prepare SF5-substituted heterocycles.

FLAP MODULATORS

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Paragraph 2426, (2015/11/03)

The present invention relates to compounds of Formula (I), or a form thereof, wherein ring A, R1, R2, R3, R3′, L, W, and V are as defined herein, useful as FLAP modulators. The invention also relates to pharmaceutical compositions comprising compounds of Formula (I). Methods of making and using the compounds of Formula (I) are also within the scope of the invention

THIOACETATE COMPOUNDS, COMPOSITIONS AND METHODS OF USE

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Page/Page column 98, (2012/01/06)

Described herein are compounds useful in the modulation of blood uric acid levels, formulations containing them and methods of using them. In some embodiments, the compounds described herein are used in the treatment or prevention of disorders related to

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