76646-42-9 Usage
Uses
Used in Food Industry:
3-HYDROXYMETHYL-4-METHOXY-BENZALDEHYDE is used as a flavoring agent for its sweet, floral aroma with a hint of almond. It is incorporated into various food products to enhance their taste and aroma, making it a valuable ingredient in the culinary world.
Used in Cosmetic Industry:
In the cosmetic industry, 3-HYDROXYMETHYL-4-METHOXY-BENZALDEHYDE serves as a fragrance component. Its pleasant and distinctive scent makes it a popular choice for adding fragrance to a wide range of cosmetic products, such as perfumes, lotions, and creams.
Used in Pharmaceutical Industry:
3-HYDROXYMETHYL-4-METHOXY-BENZALDEHYDE has been studied for its potential biological activities, including antimicrobial and antioxidant properties. These properties make it a versatile chemical that can be utilized in the development of pharmaceutical products for various therapeutic applications.
Used in Research and Development:
Due to its unique chemical structure and potential biological activities, 3-HYDROXYMETHYL-4-METHOXY-BENZALDEHYDE is also used in research and development settings. Scientists and researchers explore its properties and applications to discover new uses and improve existing products in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 76646-42-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,6,4 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 76646-42:
(7*7)+(6*6)+(5*6)+(4*4)+(3*6)+(2*4)+(1*2)=159
159 % 10 = 9
So 76646-42-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O3/c1-12-9-3-2-7(5-10)4-8(9)6-11/h2-5,11H,6H2,1H3
76646-42-9Relevant academic research and scientific papers
Alkylation of NH-, OH-, and SH-acids in the presence of potassium carbonate: 1. Functionalization of chloromethyl group of alkoxy-substituted aromatic aldehydes
Khachatryan,Razinov,Kolotaev,Belus?,Matevosyan
, p. 395 - 404 (2015/10/29)
An easily scalable, economocal, and more safe method for the preparation of 3-chloromethyl-4-methoxybenzaldehyde was developed. The latter was subjected to reactions with NH-, OH-, and SH-acids in the presence of potassium carbonate to obtain new aromatic aldehydes in high yields.
