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1,4-dioxepan-6-one is an organic compound that serves as an essential intermediate in the synthesis of various chemical products. It is characterized by its unique structure, which includes a dioxepan ring and a ketone group, making it a versatile building block in organic chemistry.

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  • 28544-93-6 Structure
  • Basic information

    1. Product Name: 1,4-dioxepan-6-one
    2. Synonyms: 1,4-dioxepan-6-one
    3. CAS NO:28544-93-6
    4. Molecular Formula: C5H8O3
    5. Molecular Weight: 116.11522
    6. EINECS: N/A
    7. Product Categories: Heterocycle-other series
    8. Mol File: 28544-93-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 218.962°C at 760 mmHg
    3. Flash Point: 76.513°C
    4. Appearance: /
    5. Density: 1.13g/cm3
    6. Vapor Pressure: 0.122mmHg at 25°C
    7. Refractive Index: 1.427
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1,4-dioxepan-6-one(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1,4-dioxepan-6-one(28544-93-6)
    12. EPA Substance Registry System: 1,4-dioxepan-6-one(28544-93-6)
  • 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: 28544-93-6(Hazardous Substances Data)

28544-93-6 Usage

Uses

Used in Chemical Synthesis:
1,4-dioxepan-6-one is used as a reactant for the synthesis of spiro ether herbicides, which are a class of compounds that exhibit herbicidal properties. These herbicides are employed in agriculture to control the growth of unwanted plants, thereby increasing crop yield and quality.
1,4-dioxepan-6-one is also used as a reactant for the synthesis of spiroheterocycl-dihydropteridinones, which are complex organic molecules with potential applications in various fields, including pharmaceuticals and materials science. The unique structure of these compounds allows for the exploration of their potential uses in drug development and other advanced applications.

Check Digit Verification of cas no

The CAS Registry Mumber 28544-93-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,5,4 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 28544-93:
(7*2)+(6*8)+(5*5)+(4*4)+(3*4)+(2*9)+(1*3)=136
136 % 10 = 6
So 28544-93-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H8O3/c6-5-3-7-1-2-8-4-5/h1-4H2

28544-93-6SDS

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 1,4-Dioxepan-6-one

1.2 Other means of identification

Product number -
Other names [1,4]Dioxepan-6-one

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:28544-93-6 SDS

28544-93-6Downstream Products

28544-93-6Relevant articles and documents

TRI-CYCLE COMPOUND AND APPLICATIONS THEREOF

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, (2020/01/22)

Disclosed in the present invention are a compound represented by formula (I), a tautomer thereof or a pharmaceutically acceptable salt, and applications thereof in the preparation of drugs for treating HBV-related diseases.

APOPTOSIS-INDUCING AGENTS FOR THE TREATMENT OF CANCER AND IMMUNE AND AUTOIMMUNE DISEASES

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, (2014/09/30)

Disclosed herein are compounds that inhibit the activity of anti-apoptotic Bcl-2 proteins, compositions containing the compounds and methods of treating diseases using the compounds.

NEW 5-ALKYNYL-PYRIDINES

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, (2012/08/08)

The present invention relates to new CGRP-antagonists of general formula I wherein R1, R2, R3, Ra, Rb, Rc, X, Y and Z are defined as mentioned hereinafter, the individual diastereomers, the individual enantiomers and the salts thereof, particularly the physiologically acceptable salts thereof with inorganic or organic acids or bases, medicaments containing these compounds, the use thereof and processes for the preparation thereof.

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