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1,2-Benzisoxazole, 5-bromo-, also known as 5-Bromo-1,2-benzisoxazole, is a chemical compound with the formula C7H4BrNO. It is a brominated derivative of benzisoxazole, characterized by the presence of a bromine atom at the 5-position. 1,2-BENZISOXAZOLE, 5-BROMOis primarily used in research and development, and has potential applications in the pharmaceutical industry.
Used in Pharmaceutical Industry:
1,2-Benzisoxazole, 5-bromois used as a building block for the synthesis of new pharmaceutical agents and drug candidates. Its unique chemical structure and reactivity make it a valuable intermediate in the development of novel therapeutics.
Used in Organic Synthesis:
1,2-Benzisoxazole, 5-bromois used as an important intermediate in organic synthesis. Its reactivity and functional groups allow for the preparation of various organic molecules, contributing to the advancement of chemical research and the discovery of new compounds.
Used in Academic and Industrial Research:
1,2-Benzisoxazole, 5-bromomay have other uses in academic and industrial research, such as in the study of chemical reactions and mechanisms. Its unique properties and reactivity can provide insights into various chemical processes and contribute to the understanding of reaction pathways and mechanisms.

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  • 837392-65-1 Structure
  • Basic information

    1. Product Name: 1,2-BENZISOXAZOLE, 5-BROMO-
    2. Synonyms: 1,2-BENZISOXAZOLE, 5-BROMO-;5-BROMOBENZO[D]ISOXAZOLE;5-BROMO-1,2-BENZISOXAZOLE;5-broMo-1,2-benzoxazole
    3. CAS NO:837392-65-1
    4. Molecular Formula: C7H4BrNO
    5. Molecular Weight: 198.02
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 837392-65-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 276.122 °C at 760 mmHg
    3. Flash Point: 120.794 °C
    4. Appearance: /
    5. Density: 1.711 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. PKA: -3.82±0.30(Predicted)
    10. CAS DataBase Reference: 1,2-BENZISOXAZOLE, 5-BROMO-(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1,2-BENZISOXAZOLE, 5-BROMO-(837392-65-1)
    12. EPA Substance Registry System: 1,2-BENZISOXAZOLE, 5-BROMO-(837392-65-1)
  • 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: 837392-65-1(Hazardous Substances Data)

837392-65-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 837392-65-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,7,3,9 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 837392-65:
(8*8)+(7*3)+(6*7)+(5*3)+(4*9)+(3*2)+(2*6)+(1*5)=201
201 % 10 = 1
So 837392-65-1 is a valid CAS Registry Number.

837392-65-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-bromo-1,2-benzoxazole

1.2 Other means of identification

Product number -
Other names 1,2-BENZISOXAZOLE,5-BROMO

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:837392-65-1 SDS

837392-65-1Downstream Products

837392-65-1Relevant articles and documents

An efficient synthesis of oxazolines: Via a cascade reaction between azaoxyallyl cations and 1,2-benzisoxazoles

Sun, Li,Liu, Yi,Wang, Yankai,Li, Yuanyuan,Liu, Zhiwen,Lu, Tao,Li, Wenhai

supporting information, p. 7526 - 7530 (2019/08/20)

A formal [3 + 2] cycloaddition reaction between the C and O terminals of azaoxyallyl cations formed in situ and 1,2-benzisoxazoles has been realized. This one-pot cycloaddition method provided an effective and practical pathway to synthesize oxazoline in good yields under mild conditions. The title products exhibited unique fluorescence properties.

Imidazole-containing condensed tricyclic compound and application thereof

-

Paragraph 0331, (2018/03/01)

The invention discloses an imidazole-containing condensed tricyclic compound adopting the structure as shown in the formula (I) or pharmaceutically acceptable salts, stereisomers or prodrug molecules thereof. The imidazole-containing condensed tricyclic compound has the IDO1 activity regulation function, can enhance T-cell activation through blocking immune checkpoints IDO1, is used for treating IDO1-mediated immunosuppression, and therefore, can become an effective medicine for treating malignant tumors. When used together with checkpoint protein anti-body drugs or other anti-cancer drugs, the imidazole-containing condensed tricyclic compound can enhance the anti-cancer effect. Meanwhile, the imidazole-containing condensed tricyclic compound has the potential of effectively treating IDO1 abnormity related immunosuppressive diseases and has a high application value.

GLUCOSYLCERAMIDE SYNTHASE INHIBITORS FOR THE TREATMENT OF DISEASES

-

Paragraph 0001054, (2015/04/15)

Described herein are compounds of Formula I, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat or prevent diseases or conditions associated with the enzyme glucosylceramide synthase (GCS).

Utility of Nitrogen Extrusion of Azido Complexes for the Synthesis of Nitriles, Benzoxazoles, and Benzisoxazoles

Nimnual, Phongprapan,Tummatorn, Jumreang,Thongsornkleeb, Charnsak,Ruchirawat, Somsak

, p. 8657 - 8667 (2015/09/15)

The utility of the nitrogen extrusion reaction of azido complexes, generated in situ from the corresponding aldehydes or ketones with TMSN3 in the presence of ZrCl4 or TfOH, has been described. These azido complexes could undergo three different pathways, depending on the substrates. First, azido methanolate complexes or imine diazonium ions could lead to benzisoxazole products via an intramolecular nucleophilic substitution. Second, imine diazonium ions could also undergo either the elimination of proton to provide nitrile products in good to excellent yields or an aryl migration, followed by an intramolecular nucleophilic addition, to give benzoxazole products in good yields.

Triflic anhydride: A mild reagent for highly efficient synthesis of 1,2-benzisoxazoles, isoxazolo, and isothiazolo quinolines without additive or base

Kalkhambkar, Rajesh G.,Yuvaraj

supporting information, p. 547 - 555 (2014/01/23)

The synthetic utility of trifluoromethanesulphonic anhydride (triflic anhydride, TA) without additive or base for the high-yielding synthesis of a wide variety of 1,2-benzisoxazoles from 2-hydroxyaryl aldoximes and ketoximes under mild conditions has been carried out for the first time. As a continuation of our study, syntheses of isoxazolo and isothiazolo quinolones have also been demonstrated using triflic anhydride under similar conditions. This method is simple and has benefits from the easy way to isolate the products in excellent yields.

A novel method for the highly efficient synthesis of 1,2-benzisoxazoles under neutral conditions using the Ph3P/DDQ system

Iranpoor, Nasser,Firouzabadi, Habib,Nowrouzi, Najmeh

, p. 8247 - 8250 (2007/10/03)

The use of Ph3P/DDQ offers a novel, neutral and highly efficient method for the efficient conversion of 2-hydroxyaryl aldoximes and ketoximes to 1,2-benzisoxazoles in excellent yields at room temperature.

Thienopyridine and furopyridine kinase inhibitors

-

, (2008/06/13)

Compounds having the formula are useful for inhibiting protein tyrosine kinases. The present invention also discloses methods of making the compounds, compositions containing the compounds, and methods of treatment using the compounds.

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