38998-17-3 Usage
Description
2,3-Dimethylanisaldehyde, also known as 2,3-dimethyl-4-methoxybenzaldehyde, is an organic compound with the molecular formula C9H10O2. It is a derivative of anisaldehyde, featuring two methyl groups at the 2nd and 3rd positions on the benzene ring and a methoxy group at the 4th position. 2,3-DIMETHYLANISALDEHYDE is known for its distinct chemical properties and potential applications in various industries.
Uses
Used in Chemical Synthesis:
2,3-Dimethylanisaldehyde is used as a key intermediate in the synthesis of various organic compounds, particularly in the preparation of β-aryl-β-ketophosphonates. These compounds are important in the development of pharmaceuticals and agrochemicals, as they can serve as building blocks for the creation of new molecules with potential biological activities.
In the pharmaceutical industry, 2,3-dimethylanisaldehyde is used as a starting material for the synthesis of various drug candidates. Its unique chemical structure allows for the development of novel molecules with potential therapeutic applications.
In the agrochemical industry, 2,3-dimethylanisaldehyde is utilized in the synthesis of new compounds with pesticidal properties. These compounds can be used to develop more effective and environmentally friendly pesticides for crop protection.
Additionally, 2,3-dimethylanisaldehyde can be used in the fragrance and flavor industry due to its distinct aromatic properties. It can be employed in the creation of new scents and flavors for various consumer products.
Check Digit Verification of cas no
The CAS Registry Mumber 38998-17-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,9,9 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 38998-17:
(7*3)+(6*8)+(5*9)+(4*9)+(3*8)+(2*1)+(1*7)=183
183 % 10 = 3
So 38998-17-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O2/c1-7-8(2)10(12-3)5-4-9(7)6-11/h4-6H,1-3H3
38998-17-3Relevant articles and documents
Process for nucleophilic fluoroalkylation of aldehydes
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, (2008/06/13)
Aryl difluoromethyl sulfone adds to alkehydes under phase transfer conditions to give novel substituted alcohols of the general formula wherein R is an aryl, cycloaliphatic, sec- or tert-aliphatic, or heterocyclic group and Ar is an aryl group. The substituted alcohols of formula I are of particular utility as intermediates in the synthesis of a variety of useful end products. For example, the products of formula I may be utilized in desulfonylation reactions, oxidation reactions and fluorination reactions.
