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2-chloro-5-[(methylthio)methyl]pyridine(SALTDATA: FREE) is a chlorinated pyridine derivative with the molecular formula C7H7ClS. It features a methylthio group in its molecular structure, making it a valuable reagent for the creation of diverse chemical compounds.

1021870-94-9

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1021870-94-9 Usage

Uses

Used in Organic Synthesis:
2-chloro-5-[(methylthio)methyl]pyridine(SALTDATA: FREE) is used as a building block for the synthesis of various molecules, contributing to the development of new chemical compounds.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2-chloro-5-[(methylthio)methyl]pyridine(SALTDATA: FREE) is used as an intermediate in the production of pharmaceuticals. Its unique structure aids in the development of new drugs.
Used in Agrochemical Production:
2-chloro-5-[(methylthio)methyl]pyridine(SALTDATA: FREE) also serves as an intermediate in the production of agrochemicals, playing a role in the creation of pesticides and other agricultural products.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-chloro-5-[(methylthio)methyl]pyridine(SALTDATA: FREE) is utilized for its potential applications in the synthesis of molecules with therapeutic properties. The presence of chloro and methylthio groups in its structure enhances its reactivity and versatility in chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 1021870-94-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,1,8,7 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1021870-94:
(9*1)+(8*0)+(7*2)+(6*1)+(5*8)+(4*7)+(3*0)+(2*9)+(1*4)=119
119 % 10 = 9
So 1021870-94-9 is a valid CAS Registry Number.

1021870-94-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-5-[(methylthio)methyl]pyridine

1.2 Other means of identification

Product number -
Other names 2-chloro-5-(methylsulfanylmethyl)pyridine

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:1021870-94-9 SDS

1021870-94-9Relevant academic research and scientific papers

SUBSTITUTED PYRIDINES FOR THE TREATMENT OF INFLAMMATORY DISEASES

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Paragraph 0211, (2021/10/22)

Compounds having the structure of Formula (I) or pharmaceutically acceptable isomers, racemates, hydrates, solvates or salts thereof, where A, R1, R2a, R2b, R2c and R3 are as defined herein, are usefu

Nitroguanidine compound and preparation and application thereof

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Paragraph 0037-0039; 0050-0051; 0052-0053; 0054-0055, (2020/04/02)

The invention relates to a nitroguanidine compound and preparation and application thereof. The nitroguanidine compound is a compound with a structure as shown in a general formula (I) which is described in the specification, or a pharmaceutically acceptable salt, enantiomer, diastereoisomer, tautomer, solvate, polymorphic substance or prodrug thereof. In the general formula (I), R1 is one selected from the group consisting of C1-C8 saturated or unsaturated aliphatic group, a benzyl group, a substituted benzyl group and a substituted pyridylmethyl group; and R2 is one selected from the group consisting of a C1-C8 saturated or unsaturated aliphatic group, a phenyl group, a substituted phenyl group and a substituted pyridyl group. Compared with the prior art, the nitroguanidine compound disclosed by the invention has a relatively good prevention effect on agricultural fungal diseases such as fusarium, gibberella, stemphylium solani, phytophthora, pythium aphanidermatum, botrytis cinerea,sclerotinia sclerotiorum and rhizoctonia solani, and can be used as a potential plant bactericide.

Heteroaryl (substituted)alkyl N-substituted sulfoximines as insecticides

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Page/Page column 7-8, (2008/12/04)

N-Substituted heteroaryl (substituted)alkyl sulfoximines are effective at controlling insects.

Use of N-substituted sulfoximines for control of invertebrate pests

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Page/Page column 2, (2008/12/04)

Methods to control certain invertebrates including insects in agricultural, urban, animal health, and industrial systems by directly or systemically applying to a locus where control is desired an effective amount of a compound of N-substituted sulfoximines.

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