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Diallyl ketone, with the chemical formula C6H10O, is a colorless to yellowish liquid characterized by a strong, onion-like odor. It is a chemical compound known for its pungent, garlic-like taste and odor, which makes it a popular ingredient in the flavoring industry.

53859-89-5

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53859-89-5 Usage

Uses

Used in Flavoring Industry:
Diallyl ketone is used as a flavoring agent for its distinctive garlic-like taste and odor, enhancing the flavor profiles of various food and beverages.
Used in Alcoholic Beverages Production:
In the alcoholic beverages industry, diallyl ketone serves as a flavor additive, contributing to the unique taste and aroma of certain products.
Used in Perfumes and Cosmetics:
Diallyl ketone is utilized as a fragrance component in perfumes and cosmetics, adding depth and complexity to scent formulations.
However, due to its toxic nature when ingested or inhaled in large amounts, and its potential carcinogenic and mutagenic properties, it is crucial to handle and use diallyl ketone with caution, adhering to safety regulations to mitigate risks of skin, eye, and respiratory system irritation.

Check Digit Verification of cas no

The CAS Registry Mumber 53859-89-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,8,5 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53859-89:
(7*5)+(6*3)+(5*8)+(4*5)+(3*9)+(2*8)+(1*9)=165
165 % 10 = 5
So 53859-89-5 is a valid CAS Registry Number.

53859-89-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name vinylmethyl ketone

1.2 Other means of identification

Product number -
Other names 1,6-heptadien-4-one

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:53859-89-5 SDS

53859-89-5Relevant academic research and scientific papers

Perfluoroalkylated Calix[4]pyrroles: Fluoride Ion Extraction from an Aqueous Medium

Maji, Sinchan,Mandal, Debaprasad

supporting information, p. 2369 - 2373 (2017/09/06)

Octaalkenyl calix[4]pyrrole ((CH2=CH(CH2)2)8C4P) is highly useful for the postfunctionalization of different calix[4]pyrroles with desired functionalities. Functionalization with perfluoroalkyl chains [CF3(CF2)n; Rfn] gave perfluoroalkyl calix[4]pyrroles (Rfn(CH2)4)8C4P; n=6, 8), having >60 % fluorine content, which created a hydrophobic environment inside the calix[4]pyrrole cavity and recognized fluoride and chloride ions in solution as well as in the solid state. The fluoride ion is extracted efficiently from aqueous CsF and TBAF solutions by using (Rf6(CH2)4)8C4P, as droplets. The fluorinated chain generated a hydrophobic environment which broke the hydration shell associated with the anion and separated out fluoride ions as droplets from aqueous medium. Furthermore, the fluoride ions competitively replaced chloride ions from the (Rf6(CH2)4)8C4P cavity.

INDOLE CARBOXAMIDES AS IKK2 INHIBITORS

-

Page/Page column 98, (2008/12/04)

The invention is directed to novel indole carboxamide compounds. Specifically, the invention is directed to compounds according to formula (I): wherein R1, R2, R3, R4, and m are as defined herein. The compounds of the invention are inhibitors of IKK2 and can be useful in the treatment of disorders associated with inappropriate IKK2 (also known as IKKβ) activity, such as rheumatoid arthritis, asthma, rhinitis, and COPD (chronic obstructive pulmonary disease). Accordingly, the invention is further directed to pharmaceutical compositions comprising a compound of the invention. The invention is still further directed to methods of inhibiting IKK2 activity and treatment of disorders associated therewith using a compound of the invention or a pharmaceutical composition comprising a compound of the invention.

Concise assembly of the polycyclic frameworks associated with the hapalindole and fischerindole alkaloids

Banwell, Martin G.,Ma, Xinghua,Taylor, Rebecca M.,Willis, Anthony C.

, p. 4959 - 4961 (2007/10/03)

Reaction of N-methylindole (4) with 6,6-dibromobicyclo[3.1.0]hexane (5) in the presence of silver tetrafluoroborate affords conjugate 7 in 67% yield. This product can be readily elaborated to compounds 12b and 13b which embody the polycyclic frameworks as

THERAPEUTICALLY USEFUL 2-AMINOTETRALIN DERIVATIVES

-

, (2008/06/13)

This invention is therapeutically useful 2-aminotetralins and pharmaceutically acceptable acid addition salts thereof of the formula STR1 R, R 1 to R 5 and p are as defined in the specification, these compounds are useful to treat central nervous system disorders, hypertension, diabetes, sexual impotency and to control appetite.

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