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Exo-3,3-Dimethyl-2-norbornanol is a bicyclic organic compound with the molecular formula C10H18O. It is a secondary alcohol, featuring a hydroxyl group (-OH) attached to a carbon atom in the norbornane ring structure. The compound is characterized by two methyl groups (-CH3) attached to the third carbon of the norbornane ring, and the hydroxyl group is positioned at the second carbon. This exo-isomer is one of the two possible isomers of 3,3-dimethyl-2-norbornanol, with the other being the endo-isomer. The exo-isomer is named as such because the hydroxyl group is positioned on the exterior side of the molecule when viewed from the perspective of the norbornane ring. exo-3,3-Dimethyl-2-norbornanol is of interest in organic chemistry due to its unique stereochemistry and potential applications in the synthesis of various pharmaceuticals and fragrances.

515-28-6

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515-28-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 515-28-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,1 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 515-28:
(5*5)+(4*1)+(3*5)+(2*2)+(1*8)=56
56 % 10 = 6
So 515-28-6 is a valid CAS Registry Number.

515-28-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3,4,4-tetrafluoro-2-(trifluoromethyl)-1,2-oxazetidine

1.2 Other means of identification

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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

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More Details:515-28-6 SDS

515-28-6Relevant academic research and scientific papers

Deamination Reactions, 40. Decomposition of 3,3-, 5,5-, and 7,7-Dimethyl-2-norbornanediazonium Ions

Kirmse, Wolfgang,Brandt, Sigrid

, p. 2510 - 2523 (2007/10/02)

gem.-Dimethylnorbornyl cations (3, 5) were generated by decomposition of optically active diazonium ion precursors. 6,1- and 6,2-H shifts were detected by structural isomerization and racemization, respectively.Product distributions and optical activities were profoundly affected by the polarity of the solvent.In weakly polar solvents, substitution reactions were associated with much less racemization than hydrogen shifts.Our observations are incompatible with equilibrating open ions but are reasonably explained in terms of unsymmetrical ion pairs.

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