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N-(2,6-Dimethylphenyl)-2-hydroxyacetamide is a chemical compound characterized by the presence of a hydroxyacetamide functional group attached to a 2,6-dimethylphenyl moiety. This structural feature endows it with potential biological activity, positioning it as a valuable building block in medicinal chemistry research. Its versatile nature and specific properties make it an important compound in the field of drug discovery and development.

29183-14-0

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29183-14-0 Usage

Uses

Used in Pharmaceutical Industry:
N-(2,6-Dimethylphenyl)-2-hydroxyacetamide is utilized as an intermediate in the synthesis of various drugs and pharmaceutical compounds. Its unique structural features contribute to the development of new therapeutic agents, enhancing the range of available treatments.
Used in Medicinal Chemistry Research:
In the realm of medicinal chemistry, N-(2,6-Dimethylphenyl)-2-hydroxyacetamide serves as a key building block for the design and synthesis of novel compounds with potential therapeutic applications. Its incorporation into molecular structures allows researchers to explore new avenues in drug discovery, potentially leading to the creation of more effective and targeted medications.
Used in Drug Discovery and Development:
N-(2,6-Dimethylphenyl)-2-hydroxyacetamide's versatility and importance in drug discovery and development are highlighted by its role in the creation of new pharmaceutical entities. N-(2,6-Dimethylphenyl)-2-hydroxyacetamide's specific properties and characteristics make it a crucial component in the advancement of medical treatments, driving innovation in healthcare.

Check Digit Verification of cas no

The CAS Registry Mumber 29183-14-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,1,8 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 29183-14:
(7*2)+(6*9)+(5*1)+(4*8)+(3*3)+(2*1)+(1*4)=120
120 % 10 = 0
So 29183-14-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO2/c1-7-4-3-5-8(2)10(7)11-9(13)6-12/h3-5,12H,6H2,1-2H3,(H,11,13)

29183-14-0SDS

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 N-(2,6-Dimethylphenyl)-2-hydroxyacetamide

1.2 Other means of identification

Product number -
Other names N-(2.6-Dimethylphenyl)-2-hydroxyacetamid

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:29183-14-0 SDS

29183-14-0Relevant academic research and scientific papers

An efficient and convenient transformation of α-haloketones to α-hydroxyketones using cesium formate

Wong, Fung Fuh,Chang, Po-Wei,Lin, Hui-Chang,You, Bang-Jau,Huang, Jiann-Jyh,Lin, Shao-Kai

supporting information; experimental part, p. 3452 - 3455 (2010/01/11)

A new safe and convenient transformation has been developed. In the presence of cesium formate in dry MeOH solution, α-haloketones underwent direct conversion reaction to afford α-hydroxyketone in excellent yields. Furthermore, this methodology can be extended and applied in 2-chloro-N-(1,3-diphenyl-1H-pyrazol-5-yl)acetamide, 2-chloro-N-(2,6-dimethylphen-yl)acetamide, 1-(bromomethylsulfonyl)benzene, and N-(bromomethyl)phthalimide to give the corresponding products in moderate to excellent yields. Crown Copyright

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