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CAS

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6281-05-6

1,1,3-trimethoxyhexane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

6281-05-6

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6281-05-6 Usage

Family

Aliphatic alcohols

Structure

Six-carbon chain with three methoxy (CH3O) groups attached to the first, first, and third carbon atoms

Usage

Reagent in chemical synthesis and solvent in various industrial applications

Appearance

Clear, colorless liquid

Odor

Faint, sweet

Health hazards

Not known to pose significant health hazards, but proper precautions should be taken when handling and storing the compound

Check Digit Verification of cas no

The CAS Registry Mumber 6281-05-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,8 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6281-05:
(6*6)+(5*2)+(4*8)+(3*1)+(2*0)+(1*5)=86
86 % 10 = 6
So 6281-05-6 is a valid CAS Registry Number.

6281-05-6SDS

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 1,1,3-trimethoxyhexane

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:6281-05-6 SDS

6281-05-6Downstream Products

6281-05-6Relevant articles and documents

Relative Reactivities of Acetals and Orthoesters in Lewis Acid Catalyzed Reactions with Vinyl Ethers. A Systematic Investigation of the Synthetic Potential of Acetals and Orthoesters in Electrophilic Alkoxyalkylations of Enol Ethers

Brueggen, Uwe von der,Lammers, Roswitha,Mayr, Herbert

, p. 2920 - 2925 (2007/10/02)

The relative reactivities of acetals and orthoesters in BF3OEt2-catalyzed reactions with methyl vinyl ether (-78 deg C, CH2Cl2) have been determined by competition experiments.A reactivity increase by 5 orders of magnitude was found in the series: saturated acetals rel values of the para-substituted benzaldehyde acetals follow a Hammett ? correlation (ρ = -4.6).Whereas the krel values of the aldehyde acetals are correlated with the corresponding rate constants of acid-catalyzed hydrolyses, ketals and orthoesters devaite from this correlation.It is concluded that the krel listing in Scheme II can be used to predict the results of Lewis acid catalyzed additions of acetals and orthoesters toward vinyl ethers: The formation of 1:1 addition products may only be expected, if the relevant functional group of the reactants is listed below the functional group of the potential 1:1 products.

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