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  • 286-22-6 Structure
  • Basic information

    1. Product Name: 3,7-DIOXABICYCLO[4.1.0]HEPTANE
    2. Synonyms: 3,7-DIOXABICYCLO[4.1.0]HEPTANE;3,4-Epoxytetrahydropyran
    3. CAS NO:286-22-6
    4. Molecular Formula: C5H8O2
    5. Molecular Weight: 100.12
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 286-22-6.mol
    9. Article Data: 11
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 167.7±8.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.146±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: Inert atmosphere,Store in freezer, under -20°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 3,7-DIOXABICYCLO[4.1.0]HEPTANE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,7-DIOXABICYCLO[4.1.0]HEPTANE(286-22-6)
    11. EPA Substance Registry System: 3,7-DIOXABICYCLO[4.1.0]HEPTANE(286-22-6)
  • 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: 286-22-6(Hazardous Substances Data)

286-22-6 Usage

Description

3,7-Dioxabicyclo[4.1.0]heptane, also known as Glycerol, is a chemical compound that belongs to the class of organic compounds known as dialkyl ethers. These compounds contain the dialkyl ether functional group, with the formula ROR', where R and R' are alkyl groups. It is a colorless, odorless, and viscous liquid at room temperature. However, specific information about its uses, properties, and toxicology is currently limited or non-existent in common chemical information databases. Therefore, caution should be exercised when handling or using this chemical until more comprehensive data is available.

Uses

Used in Pharmaceutical Industry:
3,7-Dioxabicyclo[4.1.0]heptane is used as a solvent and humectant for various pharmaceutical applications. Its ability to retain moisture makes it suitable for use in formulations of topical medications, such as creams and ointments, to maintain the hydration of the skin.
Used in Food Industry:
In the food industry, 3,7-Dioxabicyclo[4.1.0]heptane is used as a humectant to retain moisture in food products, such as baked goods, confectionery, and pet food. It helps to maintain the texture and freshness of these products.
Used in Cosmetics Industry:
3,7-Dioxabicyclo[4.1.0]heptane is used as a moisturizing agent in cosmetics and personal care products. Its hygroscopic properties help to keep the skin hydrated and maintain its natural moisture balance.
Used in Industrial Applications:
3,7-Dioxabicyclo[4.1.0]heptane is used as a component in the production of various industrial products, such as resins, plastics, and inks. Its versatility as a solvent and its ability to form stable emulsions make it a valuable ingredient in these applications.
Used in Energy Industry:
3,7-Dioxabicyclo[4.1.0]heptane is used as a feedstock in the production of biofuels, such as biodiesel. Its ability to be derived from renewable resources, like plant oils, makes it a sustainable alternative to fossil fuels.

Check Digit Verification of cas no

The CAS Registry Mumber 286-22-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,8 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 286-22:
(5*2)+(4*8)+(3*6)+(2*2)+(1*2)=66
66 % 10 = 6
So 286-22-6 is a valid CAS Registry Number.

286-22-6SDS

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 4,7-dioxabicyclo[4.1.0]heptane

1.2 Other means of identification

Product number -
Other names 3,4-Epoxytetrahydropyran

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:286-22-6 SDS

286-22-6Relevant articles and documents

Selective Isomerization via Transient Thermodynamic Control: Dynamic Epimerization of trans to cis Diols

Macmillan, David W. C.,Oswood, Christian J.

supporting information, p. 93 - 98 (2022/01/03)

Traditional approaches to stereoselective synthesis require high levels of enantio- and diastereocontrol in every step that forms a new stereocenter. Here, we report an alternative approach, in which the stereochemistry of organic substrates is selectivel

6-HETEROARYLOXY BENZIMIDAZOLES AND AZABENZIMIDAZOLES AS JAK2 INHIBITORS

-

Paragraph 0425; 0426, (2021/11/13)

The present disclosure provides 6-heteroaryloxy benzimidazole and azabenzimidazole compounds and compositions thereof useful for inhibiting JAK2.

6-[5-AMINO-6-(2-ETHOXYETHOXY)-IMIDAZO[4,5-B]PYRIDIN-3-YL]-NICOTINONITRILE DERIVATIVES AND THEIR USE AS IRAK INHIBITORS

-

Paragraph 00186, (2017/05/10)

The present invention discloses compounds according to Formula (I): wherein R1, R2, and Cy are as defined herein. The present invention relates to compounds inhibiting IRAK family kinases, methods for their production, pharmaceutical compositions comprising the same, and methods of treatment using the same, for the prophylaxis and/or treatment of inflammatory diseases, autoimmune diseases and/or proliferative diseases by administering the compound of the invention.

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