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62456-34-2

8-Bromonaphthalen-1-ylamine is a chemical compound with the molecular formula C10H8BrN. It is a derivative of naphthalene, featuring a bromine atom substituted at the 8-position and an amine functional group attached to the 1-position. This organic compound is known for its utility as a building block in the synthesis of pharmaceuticals and agrochemicals, as well as in the production of dyes, pigments, and other organic compounds. Due to its potential hazards, it is crucial to handle 8-Bromonaphthalen-1-ylamine with care to avoid skin, eye, or respiratory system contact.

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  • 62456-34-2 Structure

  • Basic information

    1. Product Name: 8-Bromonaphthalen-1-ylamine
    2. Synonyms: 8-Bromonaphthalen-1-ylamine;1-Amino-8-bromonaphthalene;8-BNA;8-bromo-1-naphthalenamine;1-Naphthalenamine, 8-bromo-
    3. CAS NO:62456-34-2
    4. Molecular Formula: C10H8BrN
    5. Molecular Weight: 222.08
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 62456-34-2.mol

  • Chemical Properties

    1. Melting Point: 82-86 °C
    2. Boiling Point: 140-150 °C(Press: 2 Torr)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.563±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 3.24±0.10(Predicted)
    10. CAS DataBase Reference: 8-Bromonaphthalen-1-ylamine(CAS DataBase Reference)
    11. NIST Chemistry Reference: 8-Bromonaphthalen-1-ylamine(62456-34-2)
    12. EPA Substance Registry System: 8-Bromonaphthalen-1-ylamine(62456-34-2)

  • 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: 62456-34-2(Hazardous Substances Data)

62456-34-2 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
8-Bromonaphthalen-1-ylamine is used as a building block for the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows for the creation of a wide range of compounds with potential therapeutic and pesticidal properties.
Used in Dye and Pigment Production:
8-Bromonaphthalen-1-ylamine is utilized in the production of dyes and pigments due to its chemical properties. Its ability to form stable compounds with color makes it a valuable component in the formulation of various dyes and pigments for different applications.
Used in Organic Compound Synthesis:
As an organic compound, 8-Bromonaphthalen-1-ylamine is used in the synthesis of other organic compounds. Its bromine and amine functional groups provide versatility in chemical reactions, enabling the creation of a diverse array of organic molecules for various purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 62456-34-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,5 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62456-34:
(7*6)+(6*2)+(5*4)+(4*5)+(3*6)+(2*3)+(1*4)=122
122 % 10 = 2
So 62456-34-2 is a valid CAS Registry Number.

62456-34-2SDS

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 8-bromonaphthalen-1-amine

1.2 Other means of identification

Product number -
Other names 1-amino-8-bromonaphthalene

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:62456-34-2 SDS

62456-34-2Relevant articles and documents

FORMATION OF PERI-FUSED HETEROCYCLES BY INTRAMOLECULAR DISPLACEMENT OF HALIDE

Herbert, John M.,Woodgate, Paul D.,Denny, William A.

, p. 1037 - 1041 (2007/10/02)

The preparation of phthaloperin-12-one and naphtho-1,3-thiazine using copper-assisted displacement of aryl halogen is described.

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