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1-oxaspiro[3.5]nonane is a spiro compound with a unique molecular structure that features a peroxide bridge and a bicyclic structure formed by the fusion of a cyclic ether with a cyclohexane ring. This organic compound is known for its structural versatility and potential biological activity.

185-18-2

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185-18-2 Usage

Uses

Used in Pharmaceutical Industry:
1-oxaspiro[3.5]nonane is used as a building block for the synthesis of various pharmaceutical compounds due to its unique molecular structure and potential biological activity.
Used in Fragrance Industry:
1-oxaspiro[3.5]nonane is used as a component in the creation of fragrances due to its structural versatility and potential to contribute to the development of novel scents.
It is important to handle and dispose of 1-oxaspiro[3.5]nonane properly to minimize health and environmental risks.

Check Digit Verification of cas no

The CAS Registry Mumber 185-18-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,8 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 185-18:
(5*1)+(4*8)+(3*5)+(2*1)+(1*8)=62
62 % 10 = 2
So 185-18-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O/c1-2-4-8(5-3-1)6-7-9-8/h1-7H2

185-18-2SDS

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-Oxaspiro[3.5]nonane

1.2 Other means of identification

Product number -
Other names 3-oxaspiro[3.5]nonane

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:185-18-2 SDS

185-18-2Relevant academic research and scientific papers

Synthesis of 2,2,-Disubstituted Oxetanes from Ketones with S-Methyl-S-(sodiomethyl)-N-(4-tolylsulfonyl)sulfoximine

Welch, Steven C.,Rao, A. S. C. Prakasa,Lyon, John T.,Assercq, Jean-Marie

, p. 252 - 257 (2007/10/02)

A covenient and facile one-step synthesis of 2,2-disubstituted oxetanes from ketones utilizing S-methyl-S-(sodiomethyl)-N-(4-tolylsulfonyl)sulfoxymine in dimethyl sulfoxide is presented.The stereochemistry and chemical reactivity of some 2,2-disubstituted

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