10031-88-6 Usage
Uses
Used in the Food Industry:
2-Heptenal, 2-ethylis used as a flavoring agent for its strong, fruity odor, enhancing the taste and aroma of various food products.
Used in the Perfume Industry:
2-Heptenal, 2-ethylis utilized in the production of perfumes, where its distinctive scent contributes to the creation of unique fragrances.
Used in Household Products:
2-Heptenal, 2-ethylserves as a scent in household products, providing a pleasant aroma to everyday items.
Used in Research and Development:
2-Heptenal, 2-ethylis studied for its potential biological and pharmacological properties, such as antimicrobial and antioxidant activities, which may lead to future applications in medicine and healthcare.
Check Digit Verification of cas no
The CAS Registry Mumber 10031-88-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,3 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10031-88:
(7*1)+(6*0)+(5*0)+(4*3)+(3*1)+(2*8)+(1*8)=46
46 % 10 = 6
So 10031-88-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O/c1-3-5-6-7-9(4-2)8-10/h7-8H,3-6H2,1-2H3/b9-7+
10031-88-6Relevant articles and documents
READILY BIODEGRADABLE ALKOXYLATE MIXTURES
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Paragraph 0037-0039; 0043, (2021/05/14)
A mixture of octanols, nonanols and decanols is useful for the preparation of alkoxylates, which alkoxylates may be used as surfactants, which surfactants have surprisingly good biodegradability.
Method for Carrying Out Multiphase Aldol Condensation Reactions to Give Mixed a, beta-Unsaturated Aldehydes
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Paragraph 0058-0061, (2014/02/15)
The invention relates to a continuous method for carrying out a multiphase aldol condensation reaction to obtain mixed α, β-unsaturated aldehydes by reacting a mixture of two aliphatic aldehydes having different numbers of carbon atoms, i.e. 2 to 5, in the molecule in a vertical tubular reactor in a concurrent flow in the presence of an aqueous solution of a basically reacting compound. In said method, the aldehyde mixture is dispersed in the aqueous phase in the form of drops, and the aqueous solution of the basically reacting compound flows through the tubular reactor as a continuous phase in laminar conditions.
