6280-51-9

Basic information

• Product Name: 2-methylphenyl 3-chlorobenzoate
• CAS NO: 6280-51-9
• Molecular Formula: C₁₄H₁₁ClO₂
• Molecular Weight: 246.6889
• Mol File: 6280-51-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 405.3°C at 760 mmHg
• Flash Point: 217.5°C
• Density: 1.226g/cm³
• Vapor Pressure: 8.87E-07mmHg at 25°C
• Refractive Index: 1.587
• CAS DataBase Reference: 2-methylphenyl 3-chlorobenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methylphenyl 3-chlorobenzoate(6280-51-9)
• EPA Substance Registry System: 2-methylphenyl 3-chlorobenzoate(6280-51-9)

Safety Data

• Hazardous Substances Data: 6280-51-9(Hazardous Substances Data)

Upstream product

• 618-46-2 m-Chlorobenzoyl chloride 
• 95-48-7 ortho-cresol 

Downstream Products

• 6280-55-3 3-chlorophenyl-(4-hydroxy-3-methylphenyl)methanone 
• 667891-41-0 ethyl 2-(4-(3-chlorobenzoyl)-2-methylphenoxy)acetate 
• 670221-36-0 2-(4-(3-chlorobenzoyl)-2-methylphenoxy)acetohydrazide 

Relevant articles and documents

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.

Benzophenone-N-ethyl piperidine ether analogues-Synthesis and efficacy as anti-inflammatory agent

A sequence of substituted benzophenone-N-ethyl piperidine ether analogues has been synthesized and evaluated as orally active anti-inflammatory agents with reduced side effects. The anti-inflammatory and ulcerogenic activities of the compounds were compared with naproxen, indomethacin, and phenylbutazone. These analogues showed an interesting anti-inflammatory activity in carrageenan-induced foot pad edema assay. In the air-pouch test, some of the analogues reduced the total number of leukocytes of the exudate, which indicates inhibition of prostaglandin production. Side effects of the compounds were examined on gastric mucosa, in the liver and stomach. None of the compounds illustrated significant side effects compared with standard drugs like indomethacin and naproxen.