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1-(1-METHYL-1H-IMIDAZOL-2-YL)-ETHANOL, also known as metomidate, is a chemical compound that serves as a sedative, hypnotic, and anesthetic agent in the medical and veterinary fields. It is a clear, colorless liquid with a faint characteristic odor, and it is soluble in both water and organic solvents. Metomidate operates by slowing down the central nervous system, which results in sedation and relaxation.
Used in Medical Applications:
1-(1-METHYL-1H-IMIDAZOL-2-YL)-ETHANOL is used as a sedative, hypnotic, and anesthetic agent for inducing sedation, relaxation, and anesthesia in patients during medical procedures. Its application is due to its ability to slow down the central nervous system, providing a calm and relaxed state for patients.
Used in Veterinary Applications:
In the veterinary industry, 1-(1-METHYL-1H-IMIDAZOL-2-YL)-ETHANOL is used as a sedative, hypnotic, and anesthetic agent for animals. It is utilized to ensure a calm and stress-free environment during veterinary procedures, similar to its use in human medicine.
Used in Neurological Condition Treatment:
1-(1-METHYL-1H-IMIDAZOL-2-YL)-ETHANOL has been studied for its potential use in the treatment of seizures and other neurological conditions. It is considered for this application because of its effects on the central nervous system, which may help in managing and alleviating symptoms associated with these conditions.

41507-36-2

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41507-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41507-36-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,5,0 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 41507-36:
(7*4)+(6*1)+(5*5)+(4*0)+(3*7)+(2*3)+(1*6)=92
92 % 10 = 2
So 41507-36-2 is a valid CAS Registry Number.

41507-36-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-methyl-3-(4-methylpiperazin-1-yl)propanoate

1.2 Other means of identification

Product number -
Other names 2-Methyl-3-[4-methyl-piperazinyl-(1)]-propionsaeure-methylester

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:41507-36-2 SDS

41507-36-2Relevant academic research and scientific papers

Asymmetric Hydroboration of Heteroaryl Ketones by Aluminum Catalysis

Lebedev, Yury,Polishchuk, Iuliia,Maity, Bholanath,Dinis Veloso Guerreiro, Miguel,Cavallo, Luigi,Rueping, Magnus

supporting information, p. 19415 - 19423 (2019/12/24)

A series of methyl aluminum complexes bearing chiral biphenol-type ligands were found to be highly active catalysts in the asymmetric reduction of heterocyclic ketones (S/C = 100-500, ee up to 99%). The protocol is suitable for a wide range of substrates and has a high tolerance to functional groups. The formed 2-heterocyclic-alcohols are valuable building blocks in drug discovery or can be used as ligands in asymmetric catalysis. Isolation and comprehensive characterization of the reaction intermediates support a catalysis cycle proposed by DFT calculations.

1 -(CYCLOPENT-2-EN-1 -YL)-3-(2-HYDROXY-3-(ARYLSULFONYL)PHENYL)UREA DERIVATIVES AS CXCR2 INHIBITORS

-

Page/Page column 66, (2015/12/18)

The invention relates to 1-(3-sulfonylphenyl)-3-(cyclopent-2-en-1-yl)urea derivatives, and their use in treating or preventing diseases and conditions mediated by the CXCR2 receptor. In addition, the invention relates to compositions containing the derivatives and processes for their preparation.

Syntheses of substituted 2-(1-methyl-2-imidazolyl)quinolines

Khazan, Minoo,Hadizadeh, Farzin,Shafiee, Abbas

, p. 1543 - 1547 (2007/10/03)

Reaction of methyllithium with 1-methyl-2-imidazolecarboxaldehyde afforded the corresponding alcohol 2. Oxidation of compound 2 with manganese dioxide gave 2-acetyl-1-methylimidazole (3). Using compound 3 and substituted isatins 4, the corresponding quinoline-4-carboxylic acids (5) were prepared. The reaction of acid imidazolides of 5 with appropriate amines yielded the amides 6. Carbamic acid esters 10 ware prepared by the Curtius rearrangement in good yield. Substituted quinolin-4-amines 13 were obtained by the acid hydrolysis of compound 10 (R1 = t-Bu). Alkylation of amines 13 with diakylaminoalkyl chlorides gave compounds 14.

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