Welcome to LookChem.com Sign In|Join Free

CAS

  • or

24021-93-0

Post Buying Request

24021-93-0 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

24021-93-0 Usage

Description

(1,2-dimethyl-1H-imidazol-5-yl)methanol, also known as DMM, is a chemical compound with the molecular formula C7H10N2O. It is a white to off-white solid with a molecular weight of 138.17 g/mol. DMM is primarily used as an intermediate for the synthesis of pharmaceutical compounds and agrochemicals. It is known for its high reactivity and can act as a ligand or catalyst in various chemical reactions. DMM is also used in the production of dyes, pigments, and other specialty chemicals. Due to its versatile applications, DMM is considered an important building block in organic synthesis and is widely used in the chemical industry.

Uses

Used in Pharmaceutical Industry:
(1,2-dimethyl-1H-imidazol-5-yl)methanol is used as an intermediate for the synthesis of pharmaceutical compounds, due to its high reactivity and ability to act as a ligand or catalyst in various chemical reactions.
Used in Agrochemical Industry:
(1,2-dimethyl-1H-imidazol-5-yl)methanol is used as an intermediate for the synthesis of agrochemicals, contributing to the development of effective and efficient products for agricultural applications.
Used in Dye and Pigment Production:
(1,2-dimethyl-1H-imidazol-5-yl)methanol is used in the production of dyes and pigments, enabling the creation of a wide range of colors and shades for various industries.
Used in Specialty Chemicals:
(1,2-dimethyl-1H-imidazol-5-yl)methanol is used in the production of specialty chemicals, serving as an important building block in organic synthesis and contributing to the development of innovative and high-quality products in the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 24021-93-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,2 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24021-93:
(7*2)+(6*4)+(5*0)+(4*2)+(3*1)+(2*9)+(1*3)=70
70 % 10 = 0
So 24021-93-0 is a valid CAS Registry Number.

24021-93-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,3-dimethylimidazol-4-yl)methanol

1.2 Other means of identification

Product number -
Other names 5-hydroxymethyl-1,2-dimethylimidazole

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:24021-93-0 SDS

24021-93-0Relevant articles and documents

PROTEIN KINASE INHIBITORS

-

Paragraph 0197, (2015/07/15)

The present invention relates to a novel family of inhibitors of protein kinases. In particular, the present invention relates to inhibitors of the members of the Tec and Src protein kinase families.

METHYL SULFANYL PYRMIDMES USEFUL AS ANTIINFLAMMATORIES, ANALGESICS, AND ANTIEPILEPTICS

-

Page/Page column 144, (2010/12/18)

The present invention relates to pyrimidine derivatives of Formula (Ia) and (Ib) (including tautomers, isomers, prodrugs, and pharmaceutically acceptable salts thereof). Said compounds are useful in the treatment of pain (such as neuropathic pain), inflammation, and epilepsy (by acting as anticonvulsants). Methods of medical treatment making use of said compounds, as well as additional compounds of Formula (IIa) and (IIb), are also disclosed.

Reactions of 1,2-Dimethylimidazole, Particularly its Metallation

Iddon, Brian,Lim, Bee Lan

, p. 271 - 277 (2007/10/02)

A re-examination of the metallation of 1,2-dimethylimidazole has shown that, after quenching of reaction mixtures with suitable reagents, single products may arise from substitution either in the 2-methyl group or in the 5-position or mixtures of both products may arise, depending on the metallating reagent, solvent, and reaction conditions. 1,2-Dimethylimidazol-5-yl-lithium was prepared by reaction of 1,2-dimethyl-5-trimethylstannylimidazole (13) with n-butyl-lithium in tetrahydrofuran at -100 deg C.The corresponding 5-trimethylsilyl compounds (12) was metallated by n-butyl-lithium exclusively in the 2-methyl group. 1,2-Dimethylimidazol-5-yl-lithium was shown to undergo transmetallation reactions at temperatures higher than -100 deg C.An improved procedure is given for the synthesis of 1,2-dimethylimidazole-5-carbaldehyde via hydroxymethylation of 1,2-dimethylimidazole and oxidation of the 5-hydroxymethyl group with nitric acid.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 24021-93-0