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1-Oxaspiro[4.5]decan-2-ol, 3-methyl- is a complex organic compound with the molecular formula C10H18O2. It is a cyclic ether with a spiro structure, consisting of a seven-membered ring fused to a five-membered ring, and a hydroxyl group attached to the second carbon of the spiro structure. The 3-methyl group indicates the presence of a methyl substituent at the third carbon of the seven-membered ring. 1-Oxaspiro[4.5]decan-2-ol, 3-methyl- is known for its unique structure and potential applications in the synthesis of various pharmaceuticals and agrochemicals. Due to its specific molecular arrangement, it may exhibit unique chemical properties and reactivity, making it a subject of interest in organic chemistry research.

87746-87-0

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87746-87-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87746-87-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,7,4 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 87746-87:
(7*8)+(6*7)+(5*7)+(4*4)+(3*6)+(2*8)+(1*7)=190
190 % 10 = 0
So 87746-87-0 is a valid CAS Registry Number.

87746-87-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-1-oxaspiro[4.5]decan-2-ol

1.2 Other means of identification

Product number -
Other names -

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

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More Details:87746-87-0 SDS

87746-87-0Relevant academic research and scientific papers

Rhodium catalysed carbonylation of homoallylic alcohols to spiropyrans bearing quaternary centres

Kitsos-Rzychon, Beate,Eilbracht, Peter

, p. 10721 - 10732 (2007/10/03)

A convenient preparation of substituted-spiropyrans via rhodium catalysed hydroformylation of homoallylic alcohols, followed by a condensation sequence to form hemiacetals and 2,2,3,3-tetraalkyl-4[H]- pyrans, is described.

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