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18102-22-2

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18102-22-2 Usage

Description

1-(Chloromethyl)-2,5-dimethyl-3-nitrobenzene is a chemical compound characterized by a benzene ring with a nitro group and two methyl groups attached at the 2nd and 5th positions. Additionally, a chloromethyl group is attached to the benzene ring, which contributes to its reactivity and potential applications in various chemical processes.

Uses

Used in Pharmaceutical Industry:
1-(Chloromethyl)-2,5-dimethyl-3-nitrobenzene is used as an intermediate in the synthesis of various pharmaceutical compounds for its ability to be further modified and incorporated into drug molecules. Its presence in the molecule can influence the pharmacological properties, such as solubility, stability, and bioavailability of the final drug product.
Used in Pesticide Industry:
In the pesticide industry, 1-(Chloromethyl)-2,5-dimethyl-3-nitrobenzene is used as a precursor in the production of certain pesticides. Its chemical structure can be tailored to create active ingredients that target specific pests, contributing to the development of more effective and selective pest control agents.
Used in Dye Industry:
1-(Chloromethyl)-2,5-dimethyl-3-nitrobenzene is utilized in the dye industry for the synthesis of various organic dyes. Its chemical structure allows for the creation of dyes with specific color properties and stability, which are important for applications in textiles, printing, and other industries that require colorants.
Safety Considerations:
Due to its potential to cause skin and eye irritation, and harmful effects if inhaled or ingested, 1-(Chloromethyl)-2,5-dimethyl-3-nitrobenzene is considered hazardous. It should be handled with care, using appropriate personal protective equipment and following safety protocols to minimize exposure and potential health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 18102-22-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,0 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 18102-22:
(7*1)+(6*8)+(5*1)+(4*0)+(3*2)+(2*2)+(1*2)=72
72 % 10 = 2
So 18102-22-2 is a valid CAS Registry Number.

18102-22-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(Chloromethyl)-2,5-dimethyl-3-nitrobenzene

1.2 Other means of identification

Product number -
Other names 6-Chlormethyl-2-nitro-p-xylol

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:18102-22-2 SDS

18102-22-2Relevant articles and documents

HETEROAROMATIC MODULATORS OF THE RETINOID-RELATED ORPHAN RECEPTOR GAMMA

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Page/Page column 67, (2018/03/28)

The present invention relates to a compound according to general formula (I) wherein X represents N or CH; R1 is -CN, (C1-C6)alkyl, (C3-C7)cycloalkyl, (3-7 membered)heterocycloalkyl, (5-6 membered)heteroaryl, (C3-C7)cycloalkyl(C1-C4)alkyl, (3-7 membered)heterocycloalkyl-(C1-C4)alkyl or (5-6 membered)heteroaryl- (C1-C4)alkyl; R2 is halogen, cyano, (C1-C4)alkyl or (C3-C7)cycloalkyl; R3 is halogen, cyano, (C1-C4)alkyl, (C1-C4)haloalkyl or (C3-C7)cycloalkyl; R4 is (C1-C4)alkyl or (C1-C4)haloalkyl; R5 is (C1-C6)alkyl, (C3-C7)cycloalkyl, (C1-C6)alkyl-(C3-C7)cycloalkyl, (C3-C7)cycloalkyl-(C1-C6)alkyl, (3-7 membered)heterocycloalkyl, phenyl, (5-6 membered)heteroaryl or -ORa. The invention further relates to said compounds for use in therapy, to pharmaceutical compositions comprising said compounds and to intermediates for preparation of said compounds.

Synthesis of potential antineoplastic agents. XXV. Approaches to the pyridocarbazole system

Winchester,Popp

, p. 547 - 549 (2007/10/05)

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