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1,2,3,4-TETRAHYDRO-NAPHTHALENE-2,7-DIAMINE, also known as tetracene, is an organic chemical compound that belongs to the class of amines. It is a diamine derivative of naphthalene, featuring two amine functional groups. Tetracene is a colorless to pale yellow solid with a melting point of 137-140°C and a boiling point of 157-160°C. It is flammable and may release toxic fumes when heated or burned, requiring proper handling and storage.

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  • 103393-75-5 Structure
  • Basic information

    1. Product Name: 1,2,3,4-TETRAHYDRO-NAPHTHALENE-2,7-DIAMINE
    2. Synonyms: 1,2,3,4-TETRAHYDRO-NAPHTHALENE-2,7-DIAMINE
    3. CAS NO:103393-75-5
    4. Molecular Formula: C10H14N2
    5. Molecular Weight: 162.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 103393-75-5.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: 1,2,3,4-TETRAHYDRO-NAPHTHALENE-2,7-DIAMINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2,3,4-TETRAHYDRO-NAPHTHALENE-2,7-DIAMINE(103393-75-5)
    11. EPA Substance Registry System: 1,2,3,4-TETRAHYDRO-NAPHTHALENE-2,7-DIAMINE(103393-75-5)
  • 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: 103393-75-5(Hazardous Substances Data)

103393-75-5 Usage

Uses

Used in Polymer Industry:
1,2,3,4-TETRAHYDRO-NAPHTHALENE-2,7-DIAMINE is used as a monomer for the production of high-performance polymers. Its unique chemical structure contributes to the development of polymers with enhanced properties, such as improved mechanical strength, thermal stability, and chemical resistance.
Used in Dye and Pigment Industry:
1,2,3,4-TETRAHYDRO-NAPHTHALENE-2,7-DIAMINE is used as a building block in the synthesis of various dyes, pigments, and pharmaceutical intermediates. Its presence in these compounds allows for the creation of a wide range of colors and properties, making it valuable in the production of inks, paints, and coatings.
Used in Oil and Gas Industry:
1,2,3,4-TETRAHYDRO-NAPHTHALENE-2,7-DIAMINE is used as a corrosion inhibitor in oil and gas production. Its ability to form protective layers on metal surfaces helps prevent corrosion, extending the lifespan of equipment and reducing maintenance costs.
Used in Rubber Industry:
1,2,3,4-TETRAHYDRO-NAPHTHALENE-2,7-DIAMINE is used as a stabilizer in the rubber industry. It helps to improve the durability and resistance of rubber products to environmental factors such as heat, light, and oxygen, ensuring their longevity and performance.

Check Digit Verification of cas no

The CAS Registry Mumber 103393-75-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,3,9 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 103393-75:
(8*1)+(7*0)+(6*3)+(5*3)+(4*9)+(3*3)+(2*7)+(1*5)=105
105 % 10 = 5
So 103393-75-5 is a valid CAS Registry Number.

103393-75-5SDS

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 1,2,3,4-tetrahydronaphthalene-2,7-diamine

1.2 Other means of identification

Product number -
Other names 1,2,3,4-TETRAHYDRO-NAPHTHALENE-2,7-DIAMINE

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:103393-75-5 SDS

103393-75-5Downstream Products

103393-75-5Relevant articles and documents

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Certain aspects of the invention relate to small molecule autophagy inhibitors, and their use for treatment and prevention of cancers and acute pancreatitis. Medicinal chemistry studies led to small molecular autophagy inhibitors with improved potency and selectivity.

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