3609-53-8 Usage
Description
METHYL 4-ACETYLBENZOATE, also known as an aromatic ketone, is a chemical compound derived from 4-bromoacetophenone. It is characterized by its white to pale yellow amorphous powder appearance and is utilized in various chemical syntheses and pharmaceutical applications.
Uses
Used in Pharmaceutical Industry:
METHYL 4-ACETYLBENZOATE is used as an intermediate compound for the synthesis of various pharmaceutical agents. Its versatile chemical structure allows it to be a key component in the development of new drugs and therapeutics.
Used in the Synthesis of 4-Methoxycarbonyl-α-Oxo-Benzeneacetic Acid:
METHYL 4-ACETYLBENZOATE serves as a crucial starting material in the preparation of 4-methoxycarbonyl-α-oxo-benzeneacetic acid, which has potential applications in the pharmaceutical industry.
Used in the Synthesis of Methyl 4-(2-(2-Methylimidazo[1,2-a]pyridin-3-yl)-2-Oxoacetyl)Benzoate:
METHYL 4-ACETYLBENZOATE is used as a building block in the synthesis of methyl 4-(2-(2-methylimidazo[1,2-a]pyridin-3-yl)-2-oxoacetyl)benzoate, which may have potential applications in various fields.
Used in the Preparation of Trisubstituted Pyrazoles:
METHYL 4-ACETYLBENZOATE is used as a key component in the preparation of trisubstituted pyrazoles, which are novel hepatitis C virus entry inhibitors. These inhibitors have potential therapeutic applications in the treatment of hepatitis C.
Check Digit Verification of cas no
The CAS Registry Mumber 3609-53-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,0 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3609-53:
(6*3)+(5*6)+(4*0)+(3*9)+(2*5)+(1*3)=88
88 % 10 = 8
So 3609-53-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H10O3/c1-7(11)8-3-5-9(6-4-8)10(12)13-2/h3-6H,1-2H3
3609-53-8Relevant articles and documents
Reaction of naphthalene-2,3-dicarbaldehyde with cyanide; a unique oxidative condensation product
McGill, Colin M.,Swearingen, Kristian E.,Drew, Kelly L.,Rasley, Brian T.,Green, Thomas K.
, p. 475 - 481 (2005)
Naphthalene-2,3-dicarbaldehyde (NDA), a reagent used for the fluorescent detection of amino acids in the presence of cyanide, self-condenses in the presence of cyanide ion and methanol at room temperature to yield a unique crystalline product 2, 15-hydroxybenzo[g]benzo[6,7]isochromeno[4,3-c]isochromen- 7(15H)-one. The product is proposed to result from facile air oxidation of NDA to a methyl ester in combination with benzoin condensation. Product 2 does not to form in the absence of air. The gHMBC spectrum of 2 distinguishes it from a possible alternative isomeric condensation product.
Visible light-mediated, high-efficiency oxidation of benzyl to acetophenone catalyzed by fluorescein
Geng, Haoxing,Liu, Xin,Zhu, Qing
supporting information, (2021/12/20)
An environmentally friendly aerobic oxidation of benzyl C(sp3)-H bonds to ketones via selective oxidation catalysis was developed. Fluorescein is an efficient photocatalyst with excellent chemical selectivity. The reaction has a wide substrate scope, and a successful gram-scale experiment demonstrated its potential industrial utility.
Novel Bortezomib prodrug and the use thereof
-
Paragraph 0088; 0090-0092; 0094-0096, (2021/07/20)
A compound of formula 1 of the invention. The optical isomer or a pharmaceutically acceptable salt thereof is a composition for bone targeting drug delivery by covalently linking a bone directional ligand binding to bone to bortezomib to overcome the tech
