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5-Hexen-3-ol, also known as leaf alcohol, is a naturally occurring organic compound with the chemical formula C6H12O. It is a colorless liquid with a strong, green, leafy odor, and is an important component in the fragrance industry. This unsaturated alcohol is found in various fruits, vegetables, and flowers, contributing to their distinct aromas. 5-Hexen-3-ol is produced through the enzymatic oxidation of linoleic acid in plants, and it plays a crucial role in plant defense mechanisms against herbivores and pathogens. In addition to its natural occurrence, 5-Hexen-3-ol is also synthesized industrially for use in perfumes, cosmetics, and food flavorings, where it helps recreate the fresh, green scent of nature.

688-99-3

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688-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 688-99-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,8 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 688-99:
(5*6)+(4*8)+(3*8)+(2*9)+(1*9)=113
113 % 10 = 3
So 688-99-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O/c1-3-5-6(7)4-2/h3,6-7H,1,4-5H2,2H3

688-99-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name hex-5-en-3-ol

1.2 Other means of identification

Product number -
Other names Aethyl-allyl-carbinol

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:688-99-3 SDS

688-99-3Relevant academic research and scientific papers

Chromium-Catalyzed Production of Diols From Olefins

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Paragraph 0111, (2021/03/19)

Processes for converting an olefin reactant into a diol compound are disclosed, and these processes include the steps of contacting the olefin reactant and a supported chromium catalyst comprising chromium in a hexavalent oxidation state to reduce at least a portion of the supported chromium catalyst to form a reduced chromium catalyst, and hydrolyzing the reduced chromium catalyst to form a reaction product comprising the diol compound. While being contacted, the olefin reactant and the supported chromium catalyst can be irradiated with a light beam at a wavelength in the UV-visible spectrum. Optionally, these processes can further comprise a step of calcining at least a portion of the reduced chromium catalyst to regenerate the supported chromium catalyst.

A MEERWEIN-PONNDORF-VERLEY TYPE REDUCTION OF α,β UNSATURATED KETONES TO ALLYLIC ALCOHOLS CATALYZED BY MgO

Kaspar, J.,Trovarelli, A.,Lenarda, M.,Graziani, M.

, p. 2705 - 2706 (2007/10/02)

Allylic alcohols are obtained with an unprecedented simple method by chemoselective hydrogen transfer reduction of α,β unsaturated ketones catalyzed by MgO.

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