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3-methyl-6-phenylhexan-3-ol is an organic compound with the molecular formula C13H20O. It is a colorless liquid with a distinct aromatic odor. 3-methyl-6-phenylhexan-3-ol is characterized by a hexane backbone, with a methyl group attached to the third carbon and a phenyl group attached to the sixth carbon. The hydroxyl group is also attached to the third carbon, making it an alcohol. 3-methyl-6-phenylhexan-3-ol is used in the synthesis of various pharmaceuticals, fragrances, and other chemical products due to its unique structure and properties. It is typically synthesized through various chemical reactions, such as the reduction of corresponding ketones or the addition of phenyl groups to alkenes.

5406-61-1

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5406-61-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5406-61-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,0 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5406-61:
(6*5)+(5*4)+(4*0)+(3*6)+(2*6)+(1*1)=81
81 % 10 = 1
So 5406-61-1 is a valid CAS Registry Number.

5406-61-1SDS

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-methyl-6-phenylhexan-3-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:5406-61-1 SDS

5406-61-1Downstream Products

5406-61-1Relevant academic research and scientific papers

Samarium diiodide mediated ketyl-aryl coupling reactions - Influence of substituents and trapping experiments

Wefelscheid, Ulrike K.,Berndt, Mathias,Reissig, Hans-Ulrich

experimental part, p. 3635 - 3646 (2009/06/06)

This comprehensive study describes the influence of substituents at the aryl moiety on SmI2-mediated intramolecular ketyl-aryl coupling reactions. Differently substituted γ-aryl ketones were employed as precursors, which were directly prepared

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