97536-45-3 Usage
Chemical Class
Dioxanes
Belongs to a group of chemical compounds that share similar structural features and properties.
Physical State
Colorless liquid
Appears as a transparent, colorless liquid without any visible color.
Odor
Strong
Possesses a potent and noticeable odor.
Solubility
Insoluble in water, soluble in organic solvents
Cannot dissolve in water but can dissolve in certain organic solvents, such as alcohols and ethers.
Usage
Flavoring agent in the food industry
Commonly used to impart flavor in various food products, particularly baked goods and confectionery items.
Application
Perfumes and fragrances
Utilized in the production of perfumes and fragrances due to its pleasant aroma.
Synthesis
Intermediate in the synthesis of other organic compounds
Serves as a starting material or building block in the creation of other organic compounds.
Potential Applications
Pharmaceutical and cosmetic industries
May have possible uses in the development of products in the pharmaceutical and cosmetic sectors.
Safety Precautions
Harmful if ingested, inhaled, or comes into contact with the skin
It is crucial to handle this chemical with care to avoid potential health risks associated with ingestion, inhalation, or skin contact.
Check Digit Verification of cas no
The CAS Registry Mumber 97536-45-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,5,3 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 97536-45:
(7*9)+(6*7)+(5*5)+(4*3)+(3*6)+(2*4)+(1*5)=173
173 % 10 = 3
So 97536-45-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H24O2/c1-10(2)7-6-8-13(5)14-11(3)9-12(4)15-13/h7,11-12H,6,8-9H2,1-5H3
97536-45-3Relevant articles and documents
1,3-dioxane derivatives, method of their synthesis and anti-peptic ulcer agent
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, (2008/06/13)
A series of new 1,3-dioxane derivatives are disclosed. These compounds have an outstanding anti-peptic ulcerative activity and are useful as novel anti-peptic ulcer agents. Such compounds are synthesized by reacting a 1,3-butanediol derivative with suitable ketone.
