24623-61-8 Usage
Description
2-hydroxy-3,5-dimethylbenzaldehyde is an organic compound with the molecular formula C7H8O2. It is a derivative of benzaldehyde, containing two methyl groups and a hydroxyl group on the aromatic ring. 2-hydroxy-3,5-dimethylbenzaldehyde has a white crystalline appearance and a characteristic almond-like odor. It is considered to be a relatively stable compound under normal conditions.
Uses
Used in Pharmaceutical Industry:
2-hydroxy-3,5-dimethylbenzaldehyde is used as a building block for the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs and medications.
Used in Fragrance Industry:
2-hydroxy-3,5-dimethylbenzaldehyde is used as a fragrance ingredient due to its characteristic almond-like odor. It contributes to the creation of various scents in perfumes, cosmetics, and other fragranced products.
Used in Agricultural Chemicals:
2-hydroxy-3,5-dimethylbenzaldehyde is used in the synthesis of agricultural chemicals. Its properties make it suitable for use in the development of pesticides, herbicides, and other agrochemicals.
Used in Flavoring Agents:
2-hydroxy-3,5-dimethylbenzaldehyde is used as a flavoring agent in the food and beverage industry. Its almond-like odor makes it a valuable component in creating flavors for various products.
Used in Organic Synthesis:
2-hydroxy-3,5-dimethylbenzaldehyde serves as an intermediate in organic synthesis. Its versatile structure allows it to be used in the production of a wide range of organic compounds for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 24623-61-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,6,2 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 24623-61:
(7*2)+(6*4)+(5*6)+(4*2)+(3*3)+(2*6)+(1*1)=98
98 % 10 = 8
So 24623-61-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O2/c1-6-3-7(2)9(11)8(4-6)5-10/h3-5,11H,1-2H3
24623-61-8Relevant articles and documents
Salicylaldimine-aluminum complexes for the facile and efficient ring-opening polymerization of ε-caprolactone
Nomura, Nobuyoshi,Aoyama, Takuji,Ishii, Ryohei,Kondo, Tadao
, p. 5363 - 5366 (2005)
A facile and efficient catalytic system of salicylaldimine-aluminum complexes for the ring-opening polymerization (ROP) of ε-caprolactone (CL) was investigated. The polymerization of Cl was examined at 25 °C in the presence of 1 mol % of benzyl alcohol (B
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Bamberger,Weiler
, p. 361 (1898)
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NOVEL SMALL MOLECULE DRUG CONJUGATES OF GEMCITABINE DERIVATIVES
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Page/Page column 63, (2019/08/26)
Disclosed are compounds having formula (I) or a pharmaceutically acceptable salt, ester, amide, solvate, or stereoisomer thereof, wherein L, Y1, Y2, Y3, Y4, Y5, Z1, Z2, Z3, Z4, Z5, Z6, and Effector are each as defined in the specification; compositions thereof; uses thereof; and methods of use thereof.
A designed protein binding-pocket to control excited-state intramolecular proton transfer fluorescence
Lampkin, Bryan J.,Monteiro, Cecilia,Powers, Evan T.,Bouc, Paige M.,Kelly, Jeffery W.,Vanveller, Brett
supporting information, p. 1076 - 1080 (2019/02/07)
Excited-state intramolecular proton transfer involves a photochemical isomerization and creates the opportunity for the emission of two distinct wavelengths of light from a single fluorophore. The selectivity between these two wavelengths of emission is d