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19225-92-4

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19225-92-4 Usage

General Description

2-(Chloromethyl)-1-methyl-1H-imidazole is an organic compound belonging to the class of imidazoles. This substance is usually depicted as a clear liquid but can also appear as a yellowish oil. As an alkyl halide, it can act as a binary compound in the presence of both chlorine and carbon but is primarily used as an intermediate to produce other chemical compounds. Due to its chemical nature, it should be handled with appropriate safety measures as it can potentially cause eye and skin irritation.

Check Digit Verification of cas no

The CAS Registry Mumber 19225-92-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,2 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19225-92:
(7*1)+(6*9)+(5*2)+(4*2)+(3*5)+(2*9)+(1*2)=114
114 % 10 = 4
So 19225-92-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H7ClN2/c1-8-3-2-7-5(8)4-6/h2-3H,4H2,1H3

19225-92-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(Chloromethyl)-1-methyl-1H-imidazole

1.2 Other means of identification

Product number -
Other names 2-(chloromethyl)-1-methylimidazole

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:19225-92-4 SDS

19225-92-4Relevant articles and documents

BICYCLIC INHIBITORS OF HISTONE DEACETYLASE

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Paragraph 00250, (2020/02/06)

Provided herein are compounds of Formula I and pharmaceutically acceptable salts and compositions thereof, which are useful for treating a variety of conditions associated with histone deacetylases (HDAC).

SULPHONAMIDE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION

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Page/Page column 67, (2010/11/28)

Disclosed are compounds having the general formula (I) as defined herein, the preparation thereof, and the use thereof for the prophylaxis or treatment of any disease involving a dysfunction associated with the orexin 2 receptor such as obesity, appetite or taste disorders including cachexia, anorexia and bulimia, diabetes, metabolic syndromes, vomiting and nausea, depression and anxiety, addictions, mood and behaviour disorders, schizophrenia, sleep disorders, restless legs syndrome, memory learning disorders, sexual and psychosexual dysfunctions, pain, visceral or neuropathic pain, hyperalgesia, allodynia, digestive disorders, irritable bowel syndrome, neuronal degenerescence, ischaemic or haemorrhagic attacks, Cushing's disease, Guillain-Barré syndrome, myotonic dystrophy, urinary incontinence, hyperthyroidism, pituitary function disorders, hypertension or hypotension.

Substituted thiazoles as immunoregulants

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, (2008/06/13)

Thiazole derivatives have been made, for example, by reacting a 2-aryl-2,2-dialkoxyethylamine with an appropriately substituted aryl acetyl halide followed by treating the resulting amide with diphosphoryl pentasulfide. The thiazole derivatives are found to be effective immunoregulants.

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