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3,9-dichlorodibenzo[c,e]oxepine-5,7-dione is a cyclic chemical compound characterized by its unique structure, which consists of two benzene rings fused to a seven-membered oxygen-containing ring. 3,9-dichlorodibenzo[c,e]oxepine-5,7-dione also features two chlorine atoms at specific positions, contributing to its electron-accepting and strong oxidizing properties. Its versatile nature and potential applications in pharmaceutical and organic chemistry make it a promising candidate for the synthesis of biologically active molecules and the development of new pharmaceuticals and organic compounds.

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  • 52767-29-0 Structure
  • Basic information

    1. Product Name: 3,9-dichlorodibenzo[c,e]oxepine-5,7-dione
    2. Synonyms:
    3. CAS NO:52767-29-0
    4. Molecular Formula: C14H6Cl2O3
    5. Molecular Weight: 293.1016
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 52767-29-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 442.4°C at 760 mmHg
    3. Flash Point: 188.8°C
    4. Appearance: N/A
    5. Density: 1.528g/cm3
    6. Vapor Pressure: 5.02E-08mmHg at 25°C
    7. Refractive Index: 1.651
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3,9-dichlorodibenzo[c,e]oxepine-5,7-dione(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3,9-dichlorodibenzo[c,e]oxepine-5,7-dione(52767-29-0)
    12. EPA Substance Registry System: 3,9-dichlorodibenzo[c,e]oxepine-5,7-dione(52767-29-0)
  • 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: 52767-29-0(Hazardous Substances Data)

52767-29-0 Usage

Uses

Used in Pharmaceutical Industry:
3,9-dichlorodibenzo[c,e]oxepine-5,7-dione is used as a precursor in the synthesis of biologically active molecules due to its unique structure and electron-accepting properties. Its potential to be further functionalized and modified in various chemical reactions makes it a valuable building block for the development of new pharmaceuticals.
Used in Organic Chemistry:
In the field of organic chemistry, 3,9-dichlorodibenzo[c,e]oxepine-5,7-dione serves as a versatile intermediate for the synthesis of complex organic compounds. Its electron-accepting and strong oxidizing properties, along with the presence of chlorine atoms, allow for a wide range of chemical reactions and modifications, enhancing its utility in creating novel organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 52767-29-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,7,6 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 52767-29:
(7*5)+(6*2)+(5*7)+(4*6)+(3*7)+(2*2)+(1*9)=140
140 % 10 = 0
So 52767-29-0 is a valid CAS Registry Number.

52767-29-0SDS

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 3,9-dichlorobenzo[d][2]benzoxepine-5,7-dione

1.2 Other means of identification

Product number -
Other names 3,9-dichlorodibenzo[c,e]oxepine-5,7-dione

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:52767-29-0 SDS

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