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Ethyl 1-oxaspiro[2.6]nonane-2-carboxylate is a chemical compound with the molecular formula C10H16O3. It is a cyclic ester derived from the spiro compound class, which consists of a spiro ring system with a seven-membered ring (nonane) and a six-membered ring (oxaspiro). The compound features an ester functional group attached to the oxaspiro ring, with an ethyl group as the alkyl substituent. Ethyl 1-oxaspiro[2.6]nonane-2-carboxylate is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain sedatives and tranquilizers. Its unique structure and properties make it a valuable building block in organic chemistry, allowing for the development of complex molecules with potential therapeutic applications.

6975-19-5

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6975-19-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6975-19-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,7 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6975-19:
(6*6)+(5*9)+(4*7)+(3*5)+(2*1)+(1*9)=135
135 % 10 = 5
So 6975-19-5 is a valid CAS Registry Number.

6975-19-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 1-oxaspiro[2.6]nonane-2-carboxylate

1.2 Other means of identification

Product number -
Other names 3,3-Hexamethylen-glycidsaeure-ethylester

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:6975-19-5 SDS

6975-19-5Downstream Products

6975-19-5Relevant academic research and scientific papers

HClO4·SiO2-mediated improved isomerization of glycidic esters to α-hydroxy-β,γ -unsaturated esters: Application in the formal synthesis of (R)-Baclofen and β-phenyl GABA analogues

Basak, Ranjan,Dharuman, Suresh,Reddy, Y. Suman,Doddi, Venkata Ramana,Vankar, Yashwant D.

supporting information; experimental part, p. 325 - 327 (2012/06/01)

An efficient isomerization of glycidic esters to corresponding allylic alcohols, viz. α-hydroxy-β,γ -unsaturated esters has been brought about using HClO4·SiO2. Five of these allylic alcohols underwent selective SN2' nucleophilic substitution to generate γ-azido-α,β-unsaturated esters which were readily converted to an antispastic drug Baclofen and four other β-phenyl GABA analogues.

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