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1-Oxaspiro[4.5]decane-4-carboxylic acid, 2-oxo-, ethyl ester is a complex organic compound with the chemical formula C12H18O4. It is a derivative of spiro[4.5]decane, a cyclic structure consisting of a seven-membered ring fused to a five-membered ring. The molecule features a carboxylic acid group at the 4-position of the spiro[4.5]decane core, which is further oxidized to a 2-oxo (keto) group. The ethyl ester functional group is attached to the carboxylic acid, making it an ester derivative. 1-Oxaspiro[4.5]decane-4-carboxylic acid, 2-oxo-, ethyl ester is primarily used in the synthesis of various pharmaceuticals and agrochemicals due to its unique structural properties and potential biological activity.

61858-03-5

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61858-03-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61858-03-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,8,5 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 61858-03:
(7*6)+(6*1)+(5*8)+(4*5)+(3*8)+(2*0)+(1*3)=135
135 % 10 = 5
So 61858-03-5 is a valid CAS Registry Number.

61858-03-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-oxo-1-oxaspiro[4,5]decane-4-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 2-oxo-1-oxaspiro[4.5]decane-4-carboxylate

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

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More Details:61858-03-5 SDS

61858-03-5Relevant academic research and scientific papers

Synthesis and photochromic properties of cycloalkylidene fulgides

Lee, Wei-Woon Wayne,Gan, Leong-Ming,Loh, Teck-Peng

, p. 2473 - 2477 (2007/10/03)

A series of cycloalkylidene fulgides have been synthesized using β,γ-unsaturated diesters, instead of the usual α,β- unsaturated diesters. A study of their photochromic properties revealed that an increase in the cycloalkylidene ring size caused a subsequ

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