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

79553-86-9

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79553-86-9 Usage

Physical state

Clear, colorless liquid

Solubility

Insoluble in water

Common uses

a. Solvent in paints, coatings, and adhesives
b. Intermediate in the synthesis of various organic compounds

Known for

a. High solvency power
b. Low volatility

Industrial applications

Preferred choice due to its properties

Safety precautions

Handle with care and follow proper safety measures when working with it

Check Digit Verification of cas no

The CAS Registry Mumber 79553-86-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,5,5 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 79553-86:
(7*7)+(6*9)+(5*5)+(4*5)+(3*3)+(2*8)+(1*6)=179
179 % 10 = 9
So 79553-86-9 is a valid CAS Registry Number.

79553-86-9SDS

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 1,1,1-triethoxyhexane

1.2 Other means of identification

Product number -
Other names Aethyl-orthocaproat

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:79553-86-9 SDS

79553-86-9Upstream product

79553-86-9Downstream Products

79553-86-9Relevant academic research and scientific papers

Synthesis method of crude carboxylic ester (by machine translation)

-

Paragraph 0021; 0022, (2020/08/09)

The method is characterized in that the carboxylic ester and the ether are prepared by reacting a carboxylic ester with an ether at a certain temperature under the catalysis of a catalyst at a certain pressure for a certain time. (by machine translation)

Process for preparation of adjacently disubstituted ketones

-

, (2008/06/13)

A novel 7-hydroxyprostaglandin E1, or a stereoisomer thereof, or a protected derivative thereof, having the following formula: STR1 wherein R8 represents H, CH3 or C2 H5, R9 represents H or CH3, R10 and R11 are identical or different, and each represents H, tetrahydropyranyl or t-butyldimethylsilyl. Also provided is a process for producing an adjacently disubstituted ketone including the above compounds, i.e. 7-oxoprostaglandin, etc. which comprises reacting an α,β-unsaturated carbonyl compound with a cuprous salt and an organolithium compound in an aprotic inert organic medium in the presence of trialkylphosphine, the amounts of said cuprous salt and said organolithium compound being substantially equimolar, and reacting the product with a protected acetal derivative of an organic carbonyl compound or an aldehyde in the presence of a Lewis acid, if necessary, followed by reacting the product with a proton donor.

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