Welcome to LookChem.com Sign In|Join Free

CAS

  • or
2-(4-bromophenyl)-6-methylbenzo[d]oxazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

891005-02-0 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 891005-02-0 Structure
  • Basic information

    1. Product Name: 2-(4-bromophenyl)-6-methylbenzo[d]oxazole
    2. Synonyms: 2-(4-bromophenyl)-6-methylbenzo[d]oxazole
    3. CAS NO:891005-02-0
    4. Molecular Formula:
    5. Molecular Weight: 288.143
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 891005-02-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(4-bromophenyl)-6-methylbenzo[d]oxazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-bromophenyl)-6-methylbenzo[d]oxazole(891005-02-0)
    11. EPA Substance Registry System: 2-(4-bromophenyl)-6-methylbenzo[d]oxazole(891005-02-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 891005-02-0(Hazardous Substances Data)

891005-02-0 Usage

Class

Benzo[d]oxazole derivatives
The compound belongs to a group of chemical compounds that are derived from benzo[d]oxazole, a heterocyclic compound with a fused benzene and oxazole ring system.
3. Heterocyclic compound
The compound contains at least one ring structure with atoms of different elements, in this case, a fused benzene and oxazole ring system.
4. Presence of bromine atom
The structure of the compound includes a bromine atom, which may influence its chemical properties, reactivity, and potential applications.
5. Presence of methyl group
The structure of the compound also includes a methyl group, which can affect its stability, reactivity, and potential applications.
6. Potential applications in organic synthesis and pharmaceutical research
Due to its unique structure and reactivity, the compound may be useful in the development of new organic synthesis methods and the discovery of new pharmaceutical compounds.
7. Safety precautions
It is important to handle and use 2-(4-bromophenyl)-6-methylbenzo[d]oxazole with care, following proper safety protocols and guidelines to minimize potential hazards to human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 891005-02-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,1,0,0 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 891005-02:
(8*8)+(7*9)+(6*1)+(5*0)+(4*0)+(3*5)+(2*0)+(1*2)=150
150 % 10 = 0
So 891005-02-0 is a valid CAS Registry Number.

891005-02-0Downstream Products

891005-02-0Relevant articles and documents

Acetyl nitrate mediated conversion of methyl ketones to diverse carboxylic acid derivatives

Bernard, Josephine,Capilato, Joseph N.,Hoy, Erik P.,Mattiucci, Joseph,Pellegrinelli, Peter J.,Perez, Lark J.,Philippi, Shane,Schnorbus, Logan

, p. 5298 - 5302 (2021/06/30)

The development of a novel acetyl nitrate mediated oxidative conversion of methyl ketones to carboxylic acid derivatives is described. By analogy to the haloform reaction and supported by experimental and computational investigation we propose a mechanism for this transformation.

Synthesis method of Tafamidis and derivative thereof

-

Paragraph 0068-0070, (2021/08/21)

The invention provides a synthesis method for preparing Tafamidis and a derivative thereof from 6-amino-m-cresol and an aldehyde compound under the action of sodium periodate and potassium permanganate. In the method, the use of an acylation reagent dichlorobenzoyl chloride and an esterification reagent (trimethylsilyl) diazomethane is avoided, and the problem that acyl chloride, a diazonium reagent, a strong acid and strong alkali additive and the like are harmful to the environment is solved; the reaction steps are few, and the total yield is high; methoxy, halogen, trifluoromethyl and the like can be well tolerated; and the iodate and the manganese dioxide after the reaction are insoluble in the reaction solution and can be well recycled, so that the pollution caused by the reaction system is greatly reduced, a more economical and environment-friendly path is provided for synthesis of Tafamidis and the derivative thereof, and the method has a huge application value.

Magnetically recoverable and reusable CuFe2O4 nanoparticle-catalyzed synthesis of benzoxazoles, benzothiazoles and benzimidazoles using dioxygen as oxidant

Yang, Daoshan,Zhu, Xiao,Wei, Wei,Sun, Nana,Yuan, Li,Jiang, Min,You, Jinmao,Wang, Hua

, p. 17832 - 17839 (2014/05/06)

A green and efficient strategy for the synthesis of benzoxazoles, benzothiazoles and benzimidazoles has been developed by using inexpensive, readily available, dioxygen-stable and recyclable CuFe2O4 as the nanocatalyst, and o-substituted aminobenzene and various aldehydes as the starting materials. The CuFe2O4 nanoparticles are dioxygen insensitive and easily recoverable with an external magnet from the reaction medium. The catalyst can be reused ten times without significant loss of catalytic activity. This journal is the Partner Organisations 2014.

Efficient indirect electrochemical synthesis of 2-substituted benzoxazoles using sodium iodide as mediator

Li, Wei-Cui,Zeng, Cheng-Chu,Hu, Li-Ming,Tian, Hong-Yu,Little, R. Daniel

, p. 2884 - 2890 (2014/03/21)

An electrochemical strategy for the effi-cient synthesis of 2-substituted benzoxazoles was de-veloped using a catalytic amount of sodium iodide (Nal) as a redox catalyst in a two-phase buffer system.

Synthesis of benzoxazoles by the copper triflate catalysed reaction of nitriles and o-aminophenols

Tan, Heng,Pan, Cheng-Xue,Xu, Yan-Li,Wang, Heng-Shan,Pan, Ying-Ming

experimental part, p. 370 - 373 (2012/09/21)

An efficient procedure for the synthesis of benzoxazoles by the heteroannulation of nitriles and o-aminophenols in the presence of a catalytic amount of copper(II) trifluoromethanesulfonate, has been developed. This method represents a practical and attractive alternative for the synthesis of both 2-arylbenzoxazoles and 2-alkylbenzoxazoles.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 891005-02-0