132350-33-5 Usage
Physical state
Colorless liquid This compound appears as a colorless liquid in its pure form.
Odor
Fruity and pungent 1-hydroxy-4-methylpentan-3-one has a distinct smell that is both fruity and pungent.
Usage
Flavoring agent It is commonly used as a flavoring agent in food and beverage products to enhance taste and aroma.
Usage
Fragrance ingredient The compound is also used as a fragrance ingredient in perfumes and cosmetics due to its pleasant odor.
Usage
Pharmaceutical production 1-hydroxy-4-methylpentan-3-one is utilized in the production of pharmaceuticals for various applications.
Safety
Relatively safe The compound is considered to be relatively safe for use in its intended applications.
Handling precautions
Handle with care It is important to handle 1-hydroxy-4-methylpentan-3-one with care to avoid any potential risks.
Storage
Cool, dry place The compound should be stored in a cool, dry place to maintain its stability and prevent any potential hazards.
Storage
Away from ignition sources 1-hydroxy-4-methylpentan-3-one should be kept away from sources of ignition to prevent accidents and ensure safe storage.
Check Digit Verification of cas no
The CAS Registry Mumber 132350-33-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,3,5 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 132350-33:
(8*1)+(7*3)+(6*2)+(5*3)+(4*5)+(3*0)+(2*3)+(1*3)=85
85 % 10 = 5
So 132350-33-5 is a valid CAS Registry Number.
132350-33-5Relevant articles and documents
SUBSTITUTED STRAIGHT CHAIN SPIRO DERIVATIVES
-
Page/Page column 107, (2021/06/26)
Provided herein are pharmaceutical agents useful for therapy and/or prophylaxis in a mammal, pharmaceutical composition comprising such compounds, and their use as menin/MLL protein/protein interaction inhibitors, useful for treating diseases such as cancer, including but not limited to leukemia, myelodysplastic syndrome (MDS), and myeloproliferative neoplasms (MPN); and diabetes.
Anionic cascade reactions. One-pot assembly of (Z)-chloro-exo- methylenetetrahydrofurans from β-hydroxyketones
Marko, Istvan E.,Schevenels, Florian T.
supporting information, p. 1319 - 1325 (2013/08/23)
The assembly of (Z)-chloro-exo-methylenetetrahydrofurans by an original and connective anionic cascade sequence is reported. Base-catalysed condensation of β-hydroxyketones with 1,1-dichloroethylene generates, in moderate to good yields, the corresponding
Efficient synthesis of α-(hydroxymethyl) ketones not available through aldol-type processes
Hitchcock,Perron,Martin,Albizati
, p. 1059 - 1061 (2007/10/02)
An efficient synthesis of α-(hydroxymethyl) ketones from β-keto esters has been developed, which is experimentally simple, amenable to large scale production and provides products of high purity without resort to chromatography in most cases. The method is a useful alternative and complement to condensation processes.
