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3-Octanone, 6-hydroxy-, also known as 6-Hydroxy-3-octanone or Capricin, is a natural organic compound with the chemical formula C8H16O2. It is a ketone derivative with a hydroxyl group attached to the sixth carbon atom in an octane chain. 3-Octanone, 6-hydroxy- is found in various plants, particularly in the essential oils of mint and basil, and is known for its pleasant, minty aroma. Capricin is used in the food and fragrance industries as a flavoring agent and a scent component. It is also recognized for its potential anti-inflammatory and antimicrobial properties, which are subjects of ongoing research.

112945-36-5

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112945-36-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112945-36-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,9,4 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 112945-36:
(8*1)+(7*1)+(6*2)+(5*9)+(4*4)+(3*5)+(2*3)+(1*6)=115
115 % 10 = 5
So 112945-36-5 is a valid CAS Registry Number.

112945-36-5SDS

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 6-hydroxyoctan-3-one

1.2 Other means of identification

Product number -
Other names 3-Octanone,6-hydroxy

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:112945-36-5 SDS

112945-36-5Upstream product

112945-36-5Downstream Products

112945-36-5Relevant academic research and scientific papers

Oxazaborolidine-catalysed reduction of alk-2-ene-1,4-diones. A convenient access to chiral 1,4-diols

Bach, Jordi,Berenguer, Ramon,Garcia, Jordi,Lopez, Marta,Manzanal, Judith,Vilarrasa, Jaume

, p. 14947 - 14962 (1998)

An efficient method for the preparation of C2-symmetric, chiral alk-2- ene-1,4-diols (4) has been achieved, based on the borane-mediated reduction of symmetric alk-2-ene-1,4-diones (2) in the presence of oxazaborolidine (R)- 1. In general, the presence of the double bond in 2 has been beneficial (compared with the related saturated 1,4-diketones 3) not only as far as the stereoselectivity in the reduction step is concerned, but also because it allowed us to remove meso-4 by chomatography and/or to improve the stereochemical purity of several resulting mixtures of diols 4 by Sharpless' epoxidation. Enantioenricbed compounds 4 have been readily reduced to saturated diols with negligible loss of optical purity.

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