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6-bromo-1,2-dihydro-2,2,4-trimethylquinoline is a quinoline derivative, a yellow solid chemical compound known for its versatile reactivity and unique structure. It is recognized for its antioxidant properties and potential as a corrosion inhibitor, with applications extending to the synthesis of pharmaceuticals, agrochemicals, and other functional materials.

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  • 91720-32-0 Structure
  • Basic information

    1. Product Name: 6-bromo-1,2-dihydro-2,2,4-trimethylquinoline
    2. Synonyms: 6-bromo-1,2-dihydro-2,2,4-trimethylquinoline;6-broMo-2,2,4-triMethyl-1,2-dihydroquinoline;Quinoline,6-bromo-1,2-dihydro-2,2,4-trimethyl-
    3. CAS NO:91720-32-0
    4. Molecular Formula: C12H14BrN
    5. Molecular Weight: 252.154
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 91720-32-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 317℃
    3. Flash Point: 145.297°C
    4. Appearance: /
    5. Density: 1.272
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.55
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: 6-bromo-1,2-dihydro-2,2,4-trimethylquinoline(CAS DataBase Reference)
    11. NIST Chemistry Reference: 6-bromo-1,2-dihydro-2,2,4-trimethylquinoline(91720-32-0)
    12. EPA Substance Registry System: 6-bromo-1,2-dihydro-2,2,4-trimethylquinoline(91720-32-0)
  • 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: 91720-32-0(Hazardous Substances Data)

91720-32-0 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
6-bromo-1,2-dihydro-2,2,4-trimethylquinoline is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity, contributing to the development of new bioactive compounds.
Used as an Antioxidant:
6-bromo-1,2-dihydro-2,2,4-trimethylquinoline is used as an antioxidant in various applications, leveraging its ability to prevent oxidative degradation and extend the shelf life of products.
Used as a Corrosion Inhibitor:
In industrial settings, 6-bromo-1,2-dihydro-2,2,4-trimethylquinoline is used as a corrosion inhibitor to protect metal surfaces from degradation, enhancing the longevity and performance of materials.
Used in Organic Light-Emitting Diodes (OLEDs):
6-bromo-1,2-dihydro-2,2,4-trimethylquinoline is utilized in the development of OLEDs, where its properties contribute to the creation of efficient and long-lasting light-emitting devices.
Used as a Fluorescent Probe in Biological Systems:
6-bromo-1,2-dihydro-2,2,4-trimethylquinoline is employed as a fluorescent probe for detecting metal ions in biological systems, offering a valuable tool for research and diagnostics.

Check Digit Verification of cas no

The CAS Registry Mumber 91720-32-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,7,2 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 91720-32:
(7*9)+(6*1)+(5*7)+(4*2)+(3*0)+(2*3)+(1*2)=120
120 % 10 = 0
So 91720-32-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H14BrN/c1-8-7-12(2,3)14-11-5-4-9(13)6-10(8)11/h4-7,14H,1-3H3

91720-32-0SDS

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 6-bromo-2,2,4-trimethyl-1H-quinoline

1.2 Other means of identification

Product number -
Other names 6-bromo-1,2-dihydro-2,2,4-trimethylquinoline

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:91720-32-0 SDS

91720-32-0Relevant articles and documents

New insight into the chemistry of selenoureas: Synthesis and single crystal structural study of diverse derivatives

Hua, Guoxiong,Du, Junyi,Carpenter-Warren, Cameron L.,Cordes, David B.,Slawin, Alexandra M.Z.,Woollins, J. Derek

, p. 7035 - 7043 (2019/05/17)

Reacting benzoyl chloride with KSeCN in acetone at room temperature, followed by treatment in situ with 4-bromoaniline led to N-((4-bromophenyl)carbamoselenoyl)benzamide in 93% yield. The same reaction was observed for 4-methoxybenzoyl chloride and 4-pent

Pinacol as a new green reducing agent: Molybdenum-catalyzed chemoselective reduction of sulfoxides and nitroaromatics

Garcia, Nuria,Garcia-Garcia, Patricia,Fernandez-Rodriguez, Manuel A.,Rubio, Ruben,Pedrosa, Maria R.,Arnaiz, Francisco J.,Sanz, Roberto

supporting information; experimental part, p. 321 - 327 (2012/04/11)

Pinacol is disclosed as a new chemoselective and environmentally benign reducing agent for sulfoxides and nitroaromatics assisted by readily available dichlorodioxomolybdenum(VI) complexes as catalysts. A wide range of substrates including those bearing challenging functional groups has been efficiently and selectively reduced with acetone and water being the only by-products of these reactions. Copyright

STEROID RECEPTOR MODULATOR COMPOUNDS AND METHODS

-

, (2008/06/13)

Non-steroidal compounds which are high affinity, high selectivity modulators for steroid receptors are disclosed. Also disclosed are pharmaceutical compositions incorporating such compounds, methods for employing the disclosed compounds and compositions for treating patients requiring steroid receptor agonist or antagonist therapy, intermediates useful in the preparation of the compounds and processes for the preparation of the steroid receptor modulator compounds.

Steroid receptor modulator compounds and methods

-

, (2008/06/13)

Non-steroidal compounds which are high affinity, high selectivity modulators for steroid receptors are disclosed. Also disclosed are pharmaceutical compositions incorporating such compounds, methods for employing the disclosed compounds and compositions for treating patients requiting steroid receptor agonist or antagonist therapy, intermediates useful in the preparation of the compounds and processes for the preparation of the steroid receptor modulator compounds.

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