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CAS

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296759-32-5

3-Bromo-2-chloro-6-nitro-quinoline is a quinoline derivative, a class of chemical compounds known for their diverse applications in various fields. This specific compound is characterized by its yellowish crystalline appearance and a molecular formula of C9H5BrClN2O2, with a molecular weight of 292.5 g/mol. Its unique properties and reactivity make it a valuable component in the synthesis of pharmaceutical products and for exploring its potential biological and pharmacological activities.

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  • 296759-32-5 Structure

  • Basic information

    1. Product Name: 3-BROMO-2-CHLORO-6-NITRO-QUINOLINE
    2. Synonyms: 3-BROMO-2-CHLORO-6-NITRO-QUINOLINE
    3. CAS NO:296759-32-5
    4. Molecular Formula: C9H4BrClN2O2
    5. Molecular Weight: 287.5
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 296759-32-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-BROMO-2-CHLORO-6-NITRO-QUINOLINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-BROMO-2-CHLORO-6-NITRO-QUINOLINE(296759-32-5)
    11. EPA Substance Registry System: 3-BROMO-2-CHLORO-6-NITRO-QUINOLINE(296759-32-5)

  • 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: 296759-32-5(Hazardous Substances Data)

296759-32-5 Usage

Uses

Used in Pharmaceutical Industry:
3-Bromo-2-chloro-6-nitro-quinoline is utilized as a key intermediate in the synthesis of various drugs and pharmaceutical products. Its unique chemical structure and reactivity contribute to the development of new and effective medications.
Used in Organic Synthesis:
3-BROMO-2-CHLORO-6-NITRO-QUINOLINE serves as an intermediate in organic synthesis, allowing for the preparation of more complex chemical compounds. Its versatility in chemical reactions makes it a valuable asset in the creation of advanced materials and specialty chemicals.
Used in Antimicrobial Applications:
3-Bromo-2-chloro-6-nitro-quinoline has been studied for its potential antimicrobial properties, making it a candidate for use in the development of new antibiotics or antimicrobial agents to combat resistant bacteria.
Used in Antiparasitic Applications:
3-BROMO-2-CHLORO-6-NITRO-QUINOLINE has also shown promise in antiparasitic research, indicating its potential use in the development of treatments for various parasitic infections.

Check Digit Verification of cas no

The CAS Registry Mumber 296759-32-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,6,7,5 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 296759-32:
(8*2)+(7*9)+(6*6)+(5*7)+(4*5)+(3*9)+(2*3)+(1*2)=205
205 % 10 = 5
So 296759-32-5 is a valid CAS Registry Number.

296759-32-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-bromo-2-chloro-6-nitroquinoline

1.2 Other means of identification

Product number -
Other names 3-BROMO-2-CHLORO-6-NITRO-QUINOLINE

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:296759-32-5 SDS

296759-32-5Downstream Products

296759-32-5Relevant articles and documents

Syntheses and binding affinities of 6-nitroquipazine analogues for serotonin transporter. Part 1

Lee, Byoung Se,Chu, Soyoung,Lee, Byung Chul,Chi, Dae Yoon,Choe, Yearn Seong,Jeong, Kyung Ja,Jin, Changbae

, p. 1559 - 1562 (2007/10/03)

6-Nitroquipazine has been known as one of the most potent and selective inhibitors of serotonin transporter in vitro and in vivo. Nine derivatives of 6-nitroquipazine were synthesized and tested for their potential abilities to displace [3H]citalopram binding to the rat cortical membranes. (C) 2000 Elsevier Science Ltd. All rights reserved.

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