122433-29-8

Basic information

• Product Name: Ethanone, 1-(2-benzoxazolyl)- (9CI)
• Synonyms: Ethanone, 1-(2-benzoxazolyl)- (9CI);Ethanone,1-(2-benzoxazolyl)-;1-(1,3-Benzoxazol-2-yl)ethanone
• CAS NO: 122433-29-8
• Molecular Formula: C₉H₇NO₂
• Molecular Weight: 161.15738
• Product Categories: ACETYLGROUP
• Mol File: 122433-29-8.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 272.9 °C at 760 mmHg
• Flash Point: 118.9 °C
• Appearance: /
• Density: 1.229 g/cm³
• Vapor Pressure: 0.00591mmHg at 25°C
• Refractive Index: 1.594
• Storage Temp.: 2-8°C
• PKA: -0.02±0.10(Predicted)
• CAS DataBase Reference: Ethanone, 1-(2-benzoxazolyl)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-(2-benzoxazolyl)- (9CI)(122433-29-8)
• EPA Substance Registry System: Ethanone, 1-(2-benzoxazolyl)- (9CI)(122433-29-8)

Safety Data

• Hazardous Substances Data: 122433-29-8(Hazardous Substances Data)

Usage

General Description

Ethanone, 1-(2-benzoxazolyl)- (9CI) is a chemical compound with the molecular formula C10H7NO2. It is classified as a ketone and contains a benzoxazolyl group. Ethanone, 1-(2-benzoxazolyl)- (9CI) is primarily used as a building block in the synthesis of various organic compounds. It has applications in the pharmaceutical and agrochemical industries, as well as in the production of specialty chemicals. Additionally, it has been studied for its potential biological activities and therapeutic properties. However, due to its potentially hazardous properties, it should be handled and used with caution in a controlled laboratory setting.

InChI:InChI=1/C9H7NO2/c1-6(11)9-10-7-4-2-3-5-8(7)12-9/h2-5H,1H3

Upstream product

• 61533-67-3 (±)-1-(1,3-benzoxazol-2-yl)ethan-1-ol 
• 124855-83-0 5a,6,11a,12-Tetrahydro-5a-methyl<1,4>benzoxazino<3,2-b><1,4>benzoxazine 
• 95-55-6 2-amino-phenol 
• 3313-37-9 benzo[d]oxazole-2-carbonitrile 
• 849585-22-4 LACTIC ACID 

Downstream Products

• 61533-67-3 (±)-1-(1,3-benzoxazol-2-yl)ethan-1-ol 
• 61841-34-7 2-isopropenylbenzoxazole 
• 124855-89-6 2-<1-(2-Benzoxazolyl)ethylidenamino>phenol 

Relevant articles and documents

Development of novel NLRP3-XOD dual inhibitors for the treatment of gout

Gout is a crystalline-related arthropathy caused by the deposition of monosodium urate (MSU). Acute gouty arthritis is the most common first symptom of gout. Studies have shown that NOD-like receptor protein 3 (NLRP3) inflammasome as pattern recognition r

Method for synthesizing benzoxazole through microwave radiation of benzamide compound in water phase

The invention discloses a method for synthesizing benzoxazole through microwave radiation of a benzamide compound in a water phase. The benzamide compound is added into the water phase under the microwave condition to be subjected to a cyclization reaction for generating the benzoxazole under the alkali condition, and the method for preparing the benzoxazole is environmentally friendly, easy and convenient to operate, safe, low in cost and efficient. Compared with the prior art, the method can be applied to a large number of functional groups, the yield is high, the number of by-products is small, and the method is easy to operate, safe, low in cost and environmentally friendly. (Please see the specifications for the formula).

Compositions containing five-membered unsaturated heterocyclic structure of the α, β unsaturated ketone compound and its preparation method and application

The invention provides alpha, beta unsaturated ketone compounds containing benzo five-membered unsaturated heterocycle structures as well as a preparation method and an application and use of the compounds. The alpha, beta unsaturated ketone compounds containing the benzo five-membered unsaturated heterocycle structures have the structure of a formula (I). In addition, the invention further provides a method for preparing the compounds and a pharmaceutical composition containing the components as active components. In vitro activity tests show that the compounds provided by the invention show a remarkable inhibiting effect on tumor cells. Therefore, the invention lays a foundation for lucubrating and developing anti-tumor medicines in the future and meanwhile further provides a new technical means for treating tumor diseases.