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1-Bicyclo[4.2.0]octa-1,3,5-trien-7-ylmethanamine is a chemical compound characterized by its unique bicyclic structure, featuring a seven-membered ring. It is a derivative of methanamine, with a cycloheptatriene group attached to the nitrogen atom. 1-Bicyclo[4.2.0]octa-1,3,5-trien-7-ylmethanamine may exhibit potential biological activity and unique chemical reactivity, making it a candidate for applications in organic synthesis and medicinal chemistry research.

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  • 1005-19-2 Structure
  • Basic information

    1. Product Name: 1-Bicyclo[4.2.0]octa-1,3,5-trien-7-ylmethanamine
    2. Synonyms: 1-Bicyclo[4.2.0]octa-1,3,5-trien-7-ylmethanamine;bicyclo[4.2.0]octa-1(6),2,4-trien-7-ylmethanamine;Bicyclo[4.2.0]octa-1,3,5-triene-7-methanamine
    3. CAS NO:1005-19-2
    4. Molecular Formula: C9H11N
    5. Molecular Weight: 133.19
    6. EINECS: N/A
    7. Product Categories: Aminomethyl's;Fused Ring Systems
    8. Mol File: 1005-19-2.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-Bicyclo[4.2.0]octa-1,3,5-trien-7-ylmethanamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Bicyclo[4.2.0]octa-1,3,5-trien-7-ylmethanamine(1005-19-2)
    11. EPA Substance Registry System: 1-Bicyclo[4.2.0]octa-1,3,5-trien-7-ylmethanamine(1005-19-2)
  • 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: 1005-19-2(Hazardous Substances Data)

1005-19-2 Usage

Uses

Used in Organic Synthesis:
1-Bicyclo[4.2.0]octa-1,3,5-trien-7-ylmethanamine is used as a building block in organic synthesis for its unique chemical reactivity, enabling the creation of novel compounds with potential applications in various fields.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 1-Bicyclo[4.2.0]octa-1,3,5-trien-7-ylmethanamine is used as a starting material or intermediate in the development of new pharmaceuticals, leveraging its potential biological activity and unique structural features.
However, it is important to note that due to the complex and potentially unstable nature of 1-Bicyclo[4.2.0]octa-1,3,5-trien-7-ylmethanamine, its practical applications may be limited. Specialized knowledge and careful handling are required to work with this compound effectively.

Check Digit Verification of cas no

The CAS Registry Mumber 1005-19-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1005-19:
(6*1)+(5*0)+(4*0)+(3*5)+(2*1)+(1*9)=32
32 % 10 = 2
So 1005-19-2 is a valid CAS Registry Number.

1005-19-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-bicyclo[4.2.0]octa-1,3,5-trienylmethanamine

1.2 Other means of identification

Product number -
Other names (Benzocyclobutenyl)methylamine

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:1005-19-2 SDS

1005-19-2Downstream Products

1005-19-2Relevant articles and documents

Benzocyclobutene end-capped imide monomer as well as preparation method and curing method thereof

-

, (2018/09/29)

The invention discloses a benzocyclobutene end-capped imide monomer as well as a preparation method and a curing method thereof. The preparation method comprises the following steps: taking o-amino benzoate as a starting material, and performing isoamyl nitrite diazotization to obtain corresponding diazonium salt, heating the diazonium salt in a 1,4-dioxane to 50 DEG C to react with acrylonitrileto obtain 1-cryanobenzocyclobutene, and performing reduction through a sodium borohydride/raney nickel system to obtain 1-aminomethyl benzocyclobutene, and reacting with aromatic anhydride through imide reaction to obtain a target monomer. The monomer has excellent processing performance, can be dissolved into various organic solvents, is relatively low in melting point, can be rotatably coated with a film or injected into a mould to cure after being directly heated to be molten or dissolved into the solvent; and moreover, the curing process only needs heating, and no byproducts are discharged.

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