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2,5,8-Trimethylquinoline, a member of the quinoline class of compounds, is a yellowish to brownish liquid characterized by a strong odor. It is recognized for its potential applications in various industries due to its chemical properties.

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  • 102871-69-2 Structure
  • Basic information

    1. Product Name: 2,5,8-TRIMETHYLQUINOLINE
    2. Synonyms: 2,5,8-TRIMETHYLQUINOLINE
    3. CAS NO:102871-69-2
    4. Molecular Formula: C12H13N
    5. Molecular Weight: 171.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 102871-69-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 278.527°C at 760 mmHg
    3. Flash Point: 114.014°C
    4. Appearance: /
    5. Density: 1.034g/cm3
    6. Vapor Pressure: 0.007mmHg at 25°C
    7. Refractive Index: 1.6
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 6.08±0.50(Predicted)
    11. CAS DataBase Reference: 2,5,8-TRIMETHYLQUINOLINE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 2,5,8-TRIMETHYLQUINOLINE(102871-69-2)
    13. EPA Substance Registry System: 2,5,8-TRIMETHYLQUINOLINE(102871-69-2)
  • 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: 102871-69-2(Hazardous Substances Data)

102871-69-2 Usage

Uses

Used in Rubber Industry:
2,5,8-Trimethylquinoline is used as a rubber antioxidant for its ability to prevent the degradation of rubber products due to oxidation. This enhances the durability and longevity of rubber goods.
Used in Chemical Production:
In the chemical industry, 2,5,8-Trimethylquinoline serves as a crucial intermediate in the production of dyes and pigments, contributing to the coloration and stability of various products.
Used in Pharmaceutical Research:
2,5,8-Trimethylquinoline is used as a subject of study for its potential biological activities, such as antioxidant and anti-inflammatory properties, which may lead to the development of new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 102871-69-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,8,7 and 1 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 102871-69:
(8*1)+(7*0)+(6*2)+(5*8)+(4*7)+(3*1)+(2*6)+(1*9)=112
112 % 10 = 2
So 102871-69-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H13N/c1-8-4-5-9(2)12-11(8)7-6-10(3)13-12/h4-7H,1-3H3

102871-69-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5,8-Trimethylquinoline

1.2 Other means of identification

Product number -
Other names 2,5,8-Trimethyl-chinolin

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:102871-69-2 SDS

102871-69-2Downstream Products

102871-69-2Relevant articles and documents

Synthesis of substituted 2-alkylquinolines by visible-light photoredox catalysis

Mei, Yousheng,Liu, Jie,Wang, Lei,Li, Pinhua

supporting information, p. 86 - 92 (2019/12/26)

The condensation of anilines and alkenyl ethers has been demonstrated by employing visible-light photoredox catalysis. The resulting method enables the synthesis of substituted 2-alkylquinolines under mild and simple conditions with good substrate scope and high yields.

Facile synthesis of 2-methylquinolines from anilines on mesoporous N-doped TiO2 under UV and visible light

Selvam,Swaminathan

, p. 500 - 508 (2013/05/21)

Nitrogen-doped TiO2 was synthesized by a simple wet method using a nitrogen precursor hydrazine hydrate and nano TiO2. This photocatalyst was characterized by X-ray diffraction, highresolution transmission electron microscopy, diffused reflectance spectra, photoluminescence, and X-ray photoelectron spectroscopy. XPS analysis indicates the incorporation of anionic nitrogen in TiO2 lattice as O-Ti-N linkage. N2 adsorption-desorpion isotherm indicates the mesoporous nature of N-TiO2 with the surface area 130.0 m2/g. Sizes of N-TiO2 particles are found to be in the range of 5-30 nm by HRTEM images. DRS spectra reveal the extended absorption to the visible range. N-TiO2 is found to be more efficient than Ag-TiO2, Au-TiO2, and Pt-TiO2 in quinaldine synthesis under visible light. Copyright Taylor & Francis Group, LLC.

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