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1-(3,5-dimethyl-1H-pyrazol-4-yl)ethanone is an organic compound characterized by its unique molecular structure, featuring a pyrazolone core with methyl groups at the 3rd and 5th positions. 1-(3,5-dimethyl-1H-pyrazol-4-yl)ethanone exhibits specific chemical properties that make it suitable for various applications, particularly in the pharmaceutical and medical fields.

1123-48-4

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1123-48-4 Usage

Uses

Used in Ophthalmic Applications:
1-(3,5-dimethyl-1H-pyrazol-4-yl)ethanone is used as a therapeutic agent for the treatment and prevention of ophthalmic diseases. Its application in this field is attributed to its potential to target specific biological pathways and mechanisms involved in the development and progression of various eye conditions, thereby offering a promising avenue for managing these disorders and improving patient outcomes.

Check Digit Verification of cas no

The CAS Registry Mumber 1123-48-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1123-48:
(6*1)+(5*1)+(4*2)+(3*3)+(2*4)+(1*8)=44
44 % 10 = 4
So 1123-48-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H10N2O/c1-4-7(6(3)10)5(2)9-8-4/h1-3H3,(H,8,9)

1123-48-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3,5-dimethyl-1H-pyrazol-4-yl)ethanone

1.2 Other means of identification

Product number -
Other names 3,5-dimethyl-4-acetylpyrazole

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:1123-48-4 SDS

1123-48-4Upstream product

1123-48-4Downstream Products

1123-48-4Relevant academic research and scientific papers

Reaction of 2-(1-alkoxyethylidene) 1,3-dicarbonyl compounds with nitrogen-containing binucleophiles

Emelina, E. E.,Ermakov, N. V.,Ershov, B. A.,Zelenin, A. K.

, p. 1637 - 1639 (2007/10/03)

The reaction of 2-(1-alkoxyethylidene) 1,3-dicarbonyl compounds with hydrazine, phenylhydrazine, urea, and dimethylhydrazine leads to high yields of the corresponding functionally substituted pyrazoles, pyrimidines, and enehydrazines.

Study of the reaction of 2-acyl 1,3-dicarbonyl compounds with hydrazines by 1H NMR spectroscopy

Emelina, E. E.,Ershov, B. A.,Zelenin, A. K.,Selivanov, S. I.

, p. 1630 - 1636 (2007/10/03)

The reaction of 2-acyl 1,3-dicarbonyl compounds with hydrazine and phenylhydrazine was studied by 1H NMR spectroscopy.It was shown that the formation of functionally 4-substituted pyrazoles is promoted if the reaction is conducted in protic solvents at reduced temperature.The presence of the benzoyl groups in the 2-acyl 1,3-dicarbonyl compounds leads to the preferential formation of the cleavage products, i.e., the corresponding acylhydrazines and 1,3-dicarbonyl compounds.It was established that the initial reaction product is consumed in two directions, i.e., cyclization with the formation of functionally 4-substituted pyyrazoles and cleavage with the formation of acetylhydrazines and the corresponding 1,3-dicarbonyl compounds.

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