7497-88-3

Basic information

• Product Name: 2-methylphenyl propanoate
• Synonyms: 2-Methylphenyl propionate; propanoic acid, 2-methylphenyl ester
• CAS NO: 7497-88-3
• Molecular Formula: C₁₀H₁₂O₂
• Molecular Weight: 164.2011
• Mol File: 7497-88-3.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 226.9°C at 760 mmHg
• Flash Point: 89.3°C
• Density: 1.027g/cm³
• Vapor Pressure: 0.0799mmHg at 25°C
• Refractive Index: 1.5
• CAS DataBase Reference: 2-methylphenyl propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methylphenyl propanoate(7497-88-3)
• EPA Substance Registry System: 2-methylphenyl propanoate(7497-88-3)

Safety Data

• Hazardous Substances Data: 7497-88-3(Hazardous Substances Data)

Usage

General Description

2-methylphenyl propanoate, also known as isobutyrophenone or 2-methylphenyl propionate, is an organic compound with the chemical formula C11H14O2. It is a colorless liquid with a sweet, fruity odor, and is commonly used as a flavoring agent in the food and beverage industry. It is also used in the production of perfumes and as a fragrance ingredient. 2-methylphenyl propanoate is synthesized through the esterification of 2-methylphenol and propanoic acid, and it is considered safe for use in food products when used in accordance with good manufacturing practices.

Upstream product

• 79-03-8 propionyl chloride 
• 95-48-7 ortho-cresol 
• 802294-64-0 propionic acid 
• 3338-15-6 1-(2-hydroxy-3-methyl-phenyl)-propan-1-one 
• 74-85-1 ethene 

Downstream Products

• 3338-15-6 1-(2-hydroxy-3-methyl-phenyl)-propan-1-one 
• 940-04-5 1-(4-hydroxy-3-methylphenyl)propan-1-one 
• 1243389-08-3 ethyl 2-bromo-6-methylbenzoate 
• 773139-06-3 ethyl 2-chloro-6-methylbenzoate 
• 1268705-48-1 (E)-2-(2-methyl-4-(1-(((5-methyl-2-(p-tolyl)oxazol-4-yl)methoxy)imino)propyl)phenoxy)acetic acid 
• 1268705-41-4 (E)-2-(2-methyl-4-(1-(((5-methyl-2-phenyloxazol-4-yl)methoxy)imino)propyl)phenoxy)acetic acid 
• 1268705-35-6 (E)-ethyl 2-(2-methyl-4-(1-(((5-methyl-2-(p-tolyl)oxazol-4-yl)methoxy)imino)propyl)phenoxy)acetate 
• 1268705-28-7 (E)-ethyl 2-(2-methyl-4-(1-(((5-methyl-2-phenyloxazol-4-yl)methoxy)imino)propyl)phenoxy)acetate 
• 1268705-22-1 (E)-2-(2-methyl-4-(1-(((4-methyl-2-(4-(trifluoromethyl)phenyl)thiazol-5-yl)methoxy)imino)propyl)phenoxy)acetic acid 
• 1268705-15-2 (E)-ethyl 2-(2-methyl-4-(1-(((4-methyl-2-(4-(trifluoromethyl)phenyl)thiazol-5-yl)methoxy)imino)propyl)phenoxy)acetate 
• 1268705-04-9 (E)-ethyl 2-(4-(1-(hydroxyimino)propyl)-2-methylphenoxy)acetate 
• 1268704-95-5 ethyl 2-(2-methyl-4-propionylphenoxy)acetate 
• 70339-98-9 1-propionoxy-2-bromomethylbenzene 

Relevant articles and documents

TETRAZOLINONE COMPOUND AND APPLICATION OF SAME

A tetrazolinone compound represented by formula (1): wherein R1 represents a C1-C3 alkyl group optionally having a fluorine atom, etc.; R2 and R4 represents a hydrogen atom, etc.; R3 represents a hydrogen atom,

TETRAZOLINONE COMPOUND AND APPLICATIONS THEREOF

Disclosed is a tetrazolinone compound having a high pest control effect and represented by the formula (1): wherein R1, R2, R3, and R11 each represent a halogen atom, a C1-C6 alkyl group, or the like; R4 and R5 each represent a hydrogen atom, a halogen atom, a C1-C3 alkyl group, or the like; R6 represents a C1-C3 alkyl group which may have a halogen atom(s) or the like; R7, R8, and R9 each represent a hydrogen atom, a halogen atom, or the like; R10 represents a C1-C3 alkyl group or the like; R12 represents a C1-C6 alkyl group, a C3-C6 cycloalkyl group, or the like, and R13 represents a C1-C6 alkyl group, a C2-C6 alkenyl group, or the like.

Therapeutically useful 1-phenyl-2-piperidinoalkanol derivatives

Compounds of the formula: STR1 wherein R1 is hydrogen, halogen, trifluoromethyl, alkyl, hydroxyl, alkyoxy, benzyloxy, alkanoyloxy, or benzoyloxy, or when R2 is hydroxyl or methoxy in the 4-position and R3 is hydrogen, R1 may also represent hydroxymethyl carbamoyl or alkoxycarbonyl, R2 is hydrogen, halogen, alkyl, hydroxyl, or alkoxy, R3 is hydrogen or alkyl, R4 is alkyl (in which case the compounds are (±)-erythro) or when R3 represents hydrogen, R4 may also be hydrogen, and R5 is hydrogen, halogen, alkyl, alkoxy, or three methoxy groups in the 3-, 4- and 5-positions and pharmaceutically acceptable acid addition salts thereof, with the exclusion of compounds wherein: (a) one of R1 and R2 is in the 4-position and is hydroxyl, alkoxy or benzyloxy, the other is in the 3-position and is hydrogen, hydroxyl, alkoxy or benzyloxy, and R3 and R5 are hydrogen and wherein: (b) R1 is in the 4-position and is halogen, R4 is methyl and R2, R3 and R5 are hydrogen, are useful as medicaments.