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71617-17-9

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71617-17-9 Usage

Group

Allyl ethers

Functionality

Carbon compounds containing an ether group with an allyl substituent

Common use

Crosslinking agent in the production of polymers, resins, and adhesives

Application

Chemical intermediate in the synthesis of other organic compounds

Industrial use

Widely used in the manufacturing of various industrial products and materials

Reactivity

Versatile

Stability

High

Toxicity

Low

Compatibility

Compatible with other chemicals

Popularity

Popular choice in the chemical industry

Check Digit Verification of cas no

The CAS Registry Mumber 71617-17-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,6,1 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 71617-17:
(7*7)+(6*1)+(5*6)+(4*1)+(3*7)+(2*1)+(1*7)=119
119 % 10 = 9
So 71617-17-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H26O2/c1-4-7-8-9-10-11-14(15-12-5-2)16-13-6-3/h5-6,14H,2-4,7-13H2,1H3

71617-17-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-bis(prop-2-enoxy)octane

1.2 Other means of identification

Product number -
Other names 1,1-Bis(allyloxy)octane

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:71617-17-9 SDS

71617-17-9Downstream Products

71617-17-9Relevant articles and documents

METHOD FOR PRODUCING 2-ALLYLCARBOXYLIC ACID COMPOUND

-

Page/Page column 19, (2008/06/13)

Disclosed is a method for commercially advantageously producing a 2-allylcarboxylic acid with high yield. Specifically disclosed is a method for producing a 2-allylcarboxylic acid compound which is characterized by the process wherein a compound represented by the formula (I) below is reacted in the presence of an acid catalyst and an allyl alcohol, thereby obtaining a 2-allylcarbonyl compound represented by the formula (II) below, and then the thus-obtained 2-allylcarbonyl compound is converted into a 2-allylcarboxylic acid represented by the formula (III) below. [Chemical formula 1] (I) [Chemical formula 2] (II) [Chemical formula 3] (III) (In the above formulae, bonds shown by solid and dotted lines represent a single bond or a double bond; X represents a formyl group, a dialkoxymethyl group or a trialkoxymethyl group; and Y represents a hydrogen atom or an alkoxy group.)

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