76472-23-6

Basic information

• Product Name: 4-(DIMETHYLCARBAMOYLMETHYL)PHENOL
• Synonyms: 4-(DIMETHYLCARBAMOYLMETHYL)PHENOL;4-(DIMETHYLCARBAMOYLMEYTHYL)PHENOL;4-(Dimethylcarbamoylmeythyl)phenol, min. 95 %;2-(4-Hydroxyphenyl)-N,N-dimethylacetamide;BenzeneacetaMide, 4-hydroxy-N,N-diMethyl-;4-[(Dimethylcarbamoyl)methyl]phenol, 4-[2-(Dimethylamino)-2-oxoethyl]phenol
• CAS NO: 76472-23-6
• Molecular Formula: C10H13NO2
• Molecular Weight: 179.22
• Mol File: 76472-23-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 346.2°C at 760 mmHg
• Flash Point: 163.2°C
• Appearance: /
• Density: 1.133g/cm³
• Vapor Pressure: 2.92E-05mmHg at 25°C
• Refractive Index: 1.554
• CAS DataBase Reference: 4-(DIMETHYLCARBAMOYLMETHYL)PHENOL(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(DIMETHYLCARBAMOYLMETHYL)PHENOL(76472-23-6)
• EPA Substance Registry System: 4-(DIMETHYLCARBAMOYLMETHYL)PHENOL(76472-23-6)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 76472-23-6(Hazardous Substances Data)

Usage

General Description

4-(Dimethylcarbamoylmethyl)phenol is an organic compound with the chemical formula C11H17NO2. This chemical is often used as a fragrance and flavoring agent in various products. It has antibacterial and antifungal properties, making it a common ingredient in personal care products such as soaps, lotions, and deodorants. Additionally, it is used in the production of pharmaceuticals and cosmetics. Its ability to inhibit the growth of microorganisms makes it a valuable ingredient in preserving products and preventing spoilage. However, it is important to note that this chemical should be handled and used with caution, as it can cause skin and eye irritation and may have harmful effects if ingested or inhaled in large quantities.

InChI:InChI=1/C10H13NO2/c1-11(2)10(13)7-8-3-5-9(12)6-4-8/h3-6,12H,7H2,1-2H3

Upstream product

• 14199-15-6 Methyl 4-hydroxyphenylacetate 
• 124-40-3 dimethyl amine 
• 156-38-7 4-hydroxyphenylacetate 
• 506-59-2 N,N-dimethylammonium chloride 

Relevant articles and documents

Synthetic method of hordenine hydrochloride

The invention discloses a synthetic method of hordenine hydrochloride. According to the synthetic method of hordenine hydrochloride, methyl 4-hydroxyphenylacetate and dimethylamine are taken as raw materials, a protonic solvent and a polar aprotic solvent are taken as solvents so as to obtain N,N-dimethyl-4-hydroxybenzeneacetamide; N,N-dimethyl-4-hydroxybenzeneacetamide is taken as a raw material, tetrahydrofuran is taken as a solvent, and a reducing agent and a catalyst are added so as to obtain hordenine; hydrochloric acid is added, ethanol is taken as a solvent, and hordenine hydrochloride is obtained via reaction. In the synthetic method, methyl 4-hydroxyphenylacetate is taken as a raw material, hordenine hydrochloride is obtained via two-step synthesis, the raw materials are easily available, the synthesis method is simple, amplification production is convenient to realize, production cost is low, industrialized production is convenient to realize, and market potential is high.

OXOTETRAHYDROFURAN-2-YL-BENZIMIDAZOLE DERIVATIVE

The present invention relates to compounds, which are useful for treatment and/or prevention of diabetes mellitus, diabetes mellitus complications or obesity, since the compounds have glucokinase-activating effects, and are presented in Formula (I): wherein R1 represents a carbamoyl group; R2 represents a lower alkyl group; both of X1 and X2 represent CH, or any one of X1 and X2 represents a nitrogen atom and the other represents CH; a group of represents a group selected from the group consisting of a pyridinyl, a pyrazinyl, a pyrazolyl, a thiadiazolyl, a triazolyl, an isoxazolyl and a thiazolyl group; and k is zero or 1, or relates to pharmaceutically acceptable salts thereof.