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3-Heptanone, 5-ethyl-5-hydroxy-4-methyl-, also known as 5-ethyl-5-hydroxy-4-methyl-3-heptanone, is an organic compound with the molecular formula C10H20O2. It is a ketone derivative, characterized by the presence of a carbonyl group (C=O) attached to a carbon atom in a heptane chain. The compound features a hydroxyl group (-OH) and an ethyl group (-CH2CH3) at the 5th carbon position, as well as a methyl group (-CH3) at the 4th carbon position. This specific arrangement of functional groups and substituents gives 3-heptanone, 5-ethyl-5-hydroxy-4-methyl- its unique chemical properties and potential applications in various fields, such as pharmaceuticals, fragrances, and chemical synthesis.

3677-86-9

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3677-86-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3677-86-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,7 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3677-86:
(6*3)+(5*6)+(4*7)+(3*7)+(2*8)+(1*6)=119
119 % 10 = 9
So 3677-86-9 is a valid CAS Registry Number.

3677-86-9SDS

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 5-ethyl-5-hydroxy-4-methylheptan-3-one

1.2 Other means of identification

Product number -
Other names 3-Heptanone,5-ethyl-5-hydroxy-4-methyl

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:3677-86-9 SDS

3677-86-9Relevant academic research and scientific papers

Synthesis of allenic diols by samarium, diiodide-promoted coupling between alkynyloxiranes and ketones

Aurrecoechea, Jose M.,Alonso, Eva,Solay, Monica

, p. 3833 - 3850 (2007/10/03)

The SmI2-mediated reductive coupling between alkynyloxiranes and ketones provides a new route to 2,3-pentadiene-1,5-diols. The preferred stereochemistry observed in the coupling products is the result of the new C- C bond forming anti with respect to the opening epoxide ring. Yields and diastereoselectivities are dependent on the alkynyloxirane substitution pattern.

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