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2-hexyl-5,5-dimethyl-1,3-dioxane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13273-90-0

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13273-90-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13273-90-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,7 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13273-90:
(7*1)+(6*3)+(5*2)+(4*7)+(3*3)+(2*9)+(1*0)=90
90 % 10 = 0
So 13273-90-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H24O2/c1-4-5-6-7-8-11-13-9-12(2,3)10-14-11/h11H,4-10H2,1-3H3

13273-90-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hexyl-5,5-dimethyl-1,3-dioxane

1.2 Other means of identification

Product number -
Other names 2-hexyl-5,5-dimethyl-1,3-dioxolane

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:13273-90-0 SDS

13273-90-0Downstream Products

13273-90-0Relevant academic research and scientific papers

Efficient and chemoselective acetalization and thioacetalization of carbonyls and subsequent deprotection using InF3 as a reusable catalyst

Madabhushi, Sridhar,Mallu, Kishore Kumar Reddy,Chinthala, Narsaiah,Beeram, China Ramanaiah,Vangipuram, Venkata Sairam

experimental part, p. 697 - 701 (2012/02/15)

An efficient and chemoselective method for preparation of acetals and dithioacetals of aldehydes and their deprotection under catalysis of InF 3 is described.

SYNTHESIS OF DIMETHYL ACETALS, DIETHYL ACETALS, AND CYCLIC ACETALS CATALYZED BY AMINOPROPYLATED SILICA GEL HYDROCHLORIDE (APSG*HCl)

Gasparrini, F.,Giovannoli, M.,Misiti, D.,Palmieri, G.

, p. 1491 - 1500 (2007/10/02)

The aminopropylated Silica-Gel hydrochloride (APSG*HCl) proved to be an efficient catalyst for the rapid conversion of carbonyl compounds in the corresponding acetals with high yields and in mild and selective conditions.In addition to the obvious advantages offered by heterogeneous catalysis, the present method results very useful when the presence of a weakly-acidic function chemically bonded on the catalyst surface (alkyl ammonium salt) is necessary (compounds which contains functions unstable in acidic media).

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