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Ketorolac

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Identification
Molecular formula
C17H17NO5
CAS number
74103-06-3
IUPAC name
(4-acetoxy-3-methyl-1-naphthyl) acetate
State
State

At room temperature, the compound is in a solid state and may exist in the form of a powder or small crystals, suitable for pharmaceutical formulations.

Melting point (Celsius)
75.00
Melting point (Kelvin)
348.10
Boiling point (Celsius)
295.80
Boiling point (Kelvin)
568.90
General information
Molecular weight
314.33g/mol
Molar mass
314.3690g/mol
Density
1.2140g/cm3
Appearence

The compound appears as a white to slightly yellow crystalline powder. It is generally odorless and is stable under normal conditions. It should be handled with care as it is used pharmaceutically.

Comment on solubility

Solubility of (4-acetoxy-3-methyl-1-naphthyl) acetate

The solubility of (4-acetoxy-3-methyl-1-naphthyl) acetate can be an interesting topic due to its unique structure and functional groups. This compound is characterized by the presence of the acetoxy and naphthyl moieties, which can significantly influence its solubility behavior in various solvents.

General Solubility Characteristics:

  • Polar Solvents: The compound may exhibit limited solubility in highly polar solvents such as water due to its non-polar naphthyl structure.
  • Non-Polar Solvents: It is likely to be more soluble in non-polar or weakly polar organic solvents like ethanol, acetone, or ether because of its hydrophobic regions.
  • Temperature Influence: The solubility may increase with temperature, making it easier to dissolve in organic solvents as they tend to have reduced intermolecular interactions at higher temperatures.

In summary, (4-acetoxy-3-methyl-1-naphthyl) acetate is anticipated to have variable solubility depending on the solvent's polarity. As a general observation, compounds similar to this one task tend to emphasize the importance of considering both functional group interactions and solvent characteristics to predict solubility adequately.

Interesting facts

Interesting Facts about (4-acetoxy-3-methyl-1-naphthyl) Acetate

(4-acetoxy-3-methyl-1-naphthyl) acetate, a derivative of naphthalene, showcases the fascinating interplay between organic chemistry and molecular functionality. This compound is characterized by its acetoxy group, which plays a critical role in its reactivity and applications. Here are some intriguing aspects of this compound:

  • Structure and Composition: The naphthalene ring structure provides stability and contributes to the interesting chemical behavior of the compound. The presence of both the acetoxy and methyl groups introduces sites for chemical transformations, making it a valuable compound in synthetic organic chemistry.
  • Applications in Synthesis: (4-acetoxy-3-methyl-1-naphthyl) acetate is often utilized as an intermediate in the synthesis of more complex molecules. Its structure allows for selective reactions that can lead to specific functional groups, proving useful in pharmaceutical and materials science research.
  • Biological Activity: Compounds related to naphthalene structures have shown various biological activities, including antibacterial, antifungal, and anti-inflammatory properties. Research into (4-acetoxy-3-methyl-1-naphthyl) acetate may reveal potential therapeutic applications.
  • Solvent Properties: Organic compounds like this naphthalene derivative typically demonstrate unique solvent properties, making them suitable for various extraction and purification processes in organic chemistry labs.
  • Chemical Research: As a subject of chemical studies, (4-acetoxy-3-methyl-1-naphthyl) acetate can be used to explore reaction mechanisms and kinetics. Understanding its reactivity can provide insights into the behavior of similar compounds.

In summary, the study of (4-acetoxy-3-methyl-1-naphthyl) acetate not only enhances our understanding of organic synthesis but also opens doors to potential innovations in biochemistry and pharmaceuticals. The ongoing exploration of such compounds is crucial in developing new materials and understanding complex biological systems.

Synonyms
Acetomenaphthone
Menadiol diacetate
Kapilin
Adaprin
Kapilon
Kayvite
Pafavit
Prokayvit oral
Kativ powder
Davitamon-K
Vitamin K diacetate
Vitavel K
Davitamon-K-oral
Kapathrom
1,4-Diacetoxy-2-methylnaphthalene
1,4-NAPHTHALENEDIOL, 2-METHYL-, DIACETATE
Menadiol di(acetate)
2-Methyl-1,4-naphthohydroquinone diacetate
2-Methyl-1,4-naphthylene diacetate
NSC 403062
DWG8UZD9HT
UNII-DWG8UZD9HT
EINECS 209-352-1
NSC-403062
BRN 1991457
DTXSID4046236
DTXCID2026236
ACETOMENAPHTHONE (MART.)
ACETOMENAPHTHONE [MART.]
209-352-1
Vitamin K4
573-20-6
2-Methylnaphthalene-1,4-diyl diacetate
Acetomenaphtone
MFCD00021469
Acetomenaphtone (JAN)
Acetomenaphthone (Menadiol Diacetate)
2-Methyl-1,4-naphthalenediol diacetate
NCGC00160567-01
Acetomenaphthone 100 microg/mL in Acetonitrile
ACETOMENAPHTONE [JAN]
Acetomenaphthone [BAN]
SMR001550632
Acetomenaphthone [INN:BAN]
2-Methylnaphthalene-1,4-diyldiacetate
Acetomenaphthone, BAN
Vitamin K4 (Standard)
(4-acetyloxy-3-methylnaphthalen-1-yl) acetate
4-(acetyloxy)-2-methylnaphthalen-1-yl acetate
1, 2-methyl-, diacetate
MLS004773967
MLS006010226
SCHEMBL209382
MENADIOL DIACETATE [MI]
CHEMBL1479848
CHEBI:31164
HY-B1508R
RYWSYCQQUDFMAU-UHFFFAOYSA-
1,4-Diacetoxy-3-methyl-naphthalin
HY-B1508
MENADIOL DIACETATE [WHO-DD]
Vitamin K4, >=98% (HPLC)
1, 4-Diacetoxy-2-methylnaphthalene
Tox21_111905
NSC403062
s4779
WLN: L66J BOV1 C1 EOV1
2-Methyl-1,4-naphthoquinol diacetate
AKOS015907780
CCG-267042
CS-8181
AS-12656
CAS-573-20-6
SY054020
4-(Acetyloxy)-2-methyl-1-naphthyl acetate
NS00033687
V0103
(4-acetyloxy-2-methylnaphthalen-1-yl) acetate
4-(Acetyloxy)-2-methyl-1-naphthyl acetate #
4-(acetyloxy)-3-methylnaphthalen-1-yl acetate
D01676
D84089
SBI-0654047.0001
SR-01000883680
SR-01000883680-1
Q27276648
InChI=1/C15H14O4/c1-9-8-14(18-10(2)16)12-6-4-5-7-13(12)15(9)19-11(3)17/h4-8H,1-3H3