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74485-37-3

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74485-37-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74485-37-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,4,8 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 74485-37:
(7*7)+(6*4)+(5*4)+(4*8)+(3*5)+(2*3)+(1*7)=153
153 % 10 = 3
So 74485-37-3 is a valid CAS Registry Number.

74485-37-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,6,9,11,14-hexaoxacyclohexadecane

1.2 Other means of identification

Product number -
Other names -

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:74485-37-3 SDS

74485-37-3Downstream Products

74485-37-3Relevant articles and documents

Miscible Polyether/Poly(ether-acetal) Electrolyte Blends

Gao, Kevin W.,Loo, Whitney S.,Snyder, Rachel L.,Abel, Brooks A.,Choo, Youngwoo,Lee, Andrew,Teixeira, Susana C. M.,Garetz, Bruce A.,Coates, Geoffrey W.,Balsara, Nitash P.

, p. 5728 - 5739 (2020/07/30)

This study shows that it is possible to obtain homogeneous mixtures of two chemically distinct polymers with a lithium salt for electrolytic applications. This approach is motivated by the success of using mixtures of organic solvents in modern lithium-io

Preparation method of cyclic acetal

-

Paragraph 0028; 0029; 0030; 0031; 0032; 0033; 0035, (2017/08/29)

The invention discloses a preparation method of cyclic acetal. The method is characterized in that long-chain polyhydroxy compounds and small-molecular aldehydes are used as the substrates, long-chain weak-polarity molecules are used as the solvent, and the aldehydes are condensed with the hydroxyl groups at two ends of the polyhydroxy compounds under the effect of a catalyst to form the intramolecular cyclic acetal. Compared with a traditional acetal preparation method, the method has the advantages that the property differences of the solvent, reactants and the substrates are utilized to allow the aldehydes to be easy to react with the hydroxyl groups, and the cyclic acetal proportion in the product is high; the conversion rate of the aldehyde compounds reaches above 80%, and the selectivity of the cyclic acetal can reach above 80%.

NMR spectra of cyclic formals formed during the early stage of the copolymerization of trioxane and ethylene oxide

Yamasaki, Naoaki,Masamoto, Junzo,Kanaori, Kenji

, p. 1069 - 1074 (2007/10/03)

During the early stage of the copolymerization of trioxane and ethylene oxide, we found the formation of three novel cyclic compounds: 1,3,5,7-tetraoxacyclononane (TOCN), 1,3,5,7,10-pentaoxacyclododecane (POCD), and 1,3,5,7,10,13-hexaoxacyclopentadecane (

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