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3,3-Dimethyl-1-oxaspiro[3,5]nonan-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22741-15-7

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22741-15-7 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 60, p. 758, 1995 DOI: 10.1021/jo00108a052

Check Digit Verification of cas no

The CAS Registry Mumber 22741-15-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,7,4 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 22741-15:
(7*2)+(6*2)+(5*7)+(4*4)+(3*1)+(2*1)+(1*5)=87
87 % 10 = 7
So 22741-15-7 is a valid CAS Registry Number.

22741-15-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3-dimethyl-1-oxaspiro[3.5]nonan-2-one

1.2 Other means of identification

Product number -
Other names 3,3-dimethyloxetan-2-one-4-spirocyclohexane

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:22741-15-7 SDS

22741-15-7Relevant academic research and scientific papers

Synthesis of α,α,β,β-Tetrasubstituted β-Lactones from Ketones, Ethyl α-Bromoisobutyrate, and Indium or Zinc. Factors Influencing the β-Lactone Formation in the Electrochemical and the Classical Procedure of the Reformatsky Reaction

Schick, Hans,Ludwig, Ralf,Schwarz, Karl-Heinz,Kleiner, Katharina,Kunath, Annamarie

, p. 3161 - 3164 (2007/10/02)

An efficient synthesis of α,α,β,β-tetrasubstituted β-lactones is achieved by an electrochemically supported Reformatsky reaction of aliphatic and aromatic ketones with ethyl α-bromoisobutyrate at a sacrificial indium anode.Under these conditions, in most

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