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6,7-Epoxyspiro[4.5]decane is a unique organic compound characterized by its molecular formula C10H16O and a molecular weight of 152.24 g/mol. It features a spiro structure, which is a type of organic compound where two rings are connected by a common atom. In this case, the spiro structure is further defined by the presence of an epoxy group, which is an oxygen atom bonded to two carbon atoms, forming a three-membered ring. 6,7-Epoxyspiro[4.5]decane is of interest in organic chemistry due to its potential applications in the synthesis of various complex molecules and its structural properties. It is also known for its role in the formation of certain natural products and its potential use as an intermediate in the production of pharmaceuticals and other specialty chemicals.

187-24-6

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187-24-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 187-24-6 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 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 187-24:
(5*1)+(4*8)+(3*7)+(2*2)+(1*4)=66
66 % 10 = 6
So 187-24-6 is a valid CAS Registry Number.

187-24-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name spiro[7-oxabicyclo[4.1.0]heptane-5,1'-cyclopentane]

1.2 Other means of identification

Product number -
Other names 6,7-Epoxy-spiro<4,5>decan

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:187-24-6 SDS

187-24-6Upstream product

187-24-6Relevant academic research and scientific papers

Fragmentation of nitrone triflates to 9-membered rings

Murphy, John A.,Mahesh, Mohan,McPheators, Gary,Vijaya Anand,McGuire, Thomas M.,Carlinga, Robert,Kennedy, Alan R.

, p. 3233 - 3236 (2007)

A new fragmentative rearrangement of nitrone derivatives to form 9-membered rings is reported. The fragmentations are triggered when nitrones are treated with triflic anhydride; a C-C bond antiperiplanar to the cleaving N-O bond is activated either by an oxygen lone pair or by an electron-rich aromatic ring. In the former case, further cyclization of the 9-membered intermediate leads to a rearranged condensed ring system, but when triggered by arenes, 9-membered ring amides are isolated.

Novel Catalytic Kinetic Resolution of Racemic Epoxides to Allylic Alcohols

Gayet, Arnaud,Bertilsson, Sophie,Andersson, Pher G.

, p. 3777 - 3779 (2007/10/03)

(Matrix Presented) The kinetic resolution of racemic epoxides via catalytic enantioselective rearrangement to allylic alcohols was investigated. Using the Li-salt of (1S,3R,4R)-3-(pyrrolidinyl)methyl-2-azabicyclo [2.2.1] heptane 1 as catalyst allowed both

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