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189509-22-6

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  • SAGECHEM/Ethyl 2-(8-hydroxy-1,4-dioxaspiro[4.5]decan-8-yl)acetate/SAGECHEM/Manufacturer in China

    Cas No: 189509-22-6

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189509-22-6 Usage

General Description

1,4-Dioxaspiro[4.5]decane-8-acetic acid, 8-hydroxy-, ethyl ester is a chemical compound that belongs to the ester class of organic compounds. It is commonly used as a solvent, in the production of pharmaceuticals and as a fragrance. This chemical is known for its ability to dissolve other substances and is often used in industrial applications. It has a molecular formula of C12H20O4 and a molecular weight of 228.28 g/mol. 1,4-Dioxaspiro[4.5]decane-8-acetic acid, 8-hydroxy-, ethyl ester may have potential applications in various industries due to its unique properties and may be subject to regulation in certain jurisdictions due to its chemical nature.

Check Digit Verification of cas no

The CAS Registry Mumber 189509-22-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,5,0 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 189509-22:
(8*1)+(7*8)+(6*9)+(5*5)+(4*0)+(3*9)+(2*2)+(1*2)=176
176 % 10 = 6
So 189509-22-6 is a valid CAS Registry Number.

189509-22-6SDS

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 ethyl 2-(8-hydroxy-1,4-dioxaspiro[4.5]decan-8-yl)acetate

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:189509-22-6 SDS

189509-22-6Relevant articles and documents

An iodine catalyzed metal free domino process for the stereoselective synthesis of oxygen bridged bicyclic ethers

Subba Reddy,Someswarao,Prudhviraju,Reddy, B. Jagan Mohan,Sridhar,Kiran Kumar

supporting information, p. 6737 - 6741 (2015/06/25)

A domino reaction has been developed for the synthesis of oxygen bridged bicyclic ethers through the coupling of 4-(2-hydroxyethyl)cyclohex-3-enols with aldehydes in the presence of 10 mol% of molecular iodine in dichloromethane at 25 °C. This method is h

Synthesis of 13C-labeled possible intermediates in the biosynthesis of phenylethanoid derivatives, cornoside and rengyosides

Kuwajima, Hiroshi,Takai, Yoshitaka,Takaishi, Kiyokazu,Inoue, Kenichiro

, p. 581 - 586 (2007/10/03)

In order to clarify the biosynthetic pathway of C6-C2 unit compounds containing salidroside, cornoside, and rengyosides A and B in oleaceous plants, 13C-labeled putative precursors, 4-hydroxyphenylethanol, salidroside and cornoside, were prepared.

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