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1,4,7,12,15,18-hexaoxacyclodocosane-8,11,19,22-tetrone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77022-93-6

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77022-93-6 Usage

Class

Cyclic ethers

Molecular weight

456.39 g/mol

Structure

A cyclic compound with six oxygen atoms and twenty-four carbon atoms

Polymeric materials

Used in the production of resins, coatings, and adhesives

Pharmaceutical industry

Potential use as a drug delivery agent

Food industry

Potential use as a food additive

Bonding properties

Ability to form strong and stable bonds

Versatility

Unique structure and properties make it suitable for various potential uses in different industries

Check Digit Verification of cas no

The CAS Registry Mumber 77022-93-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,0,2 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 77022-93:
(7*7)+(6*7)+(5*0)+(4*2)+(3*2)+(2*9)+(1*3)=126
126 % 10 = 6
So 77022-93-6 is a valid CAS Registry Number.
InChI:InChI=1/C16H24O10/c17-13-1-2-14(18)24-10-6-22-8-12-26-16(20)4-3-15(19)25-11-7-21-5-9-23-13/h1-12H2

77022-93-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4,7,12,15,18-hexaoxacyclodocosane-8,11,19,22-tetrone

1.2 Other means of identification

Product number -
Other names 1,6,9,12,17,20-hexaoxacyclodocosane-2,5,13,16-tetraone

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:77022-93-6 SDS

77022-93-6Downstream Products

77022-93-6Relevant academic research and scientific papers

Synthesis of Macrocyclic Lactones and Ether Lactones under Solid-Liquid Phase Transfer Conditions

Singh, Paramjit,Kumar, Manoj,Singh, Harjit

, p. 64 - 65 (2007/10/02)

Phase transfer catalysed condensation of diacid halides and diols gives the title compounds in improved yields.

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