Acetomenaphthone

A summary of the most common chemical descriptors (InChI Key and SMILES codes) for Acetomenaphthone are summarized together with 3D and 2D structures and relevant physico-chemical properties.

What is the Acetomenaphthone?

The molecule Acetomenaphthone presents a molecular formula of C16H14F3N3OS and its IUPAC name is (4-acetyloxy-3-methylnaphthalen-1-yl) acetate.

Acetomenaphthone is a molecule that consists of a benzene ring with a ketone group attached to it. The ketone group makes this molecule a good candidate for use as a solvent or as a reagent in organic synthesis..

3D structure

Cartesian coordinates

Geometry of Acetomenaphthone in x, y and z coordinates (Å units) to copy/paste elsewhere. Generated with Open Babel software.

2D drawing

 

Acetomenaphthone RZSYMONMXLYBMJ-UHFFFAOYSA-N chemical compound 2D structure molecule svg
Acetomenaphthone

 

Molecule descriptors

 
IUPAC name(4-acetyloxy-3-methylnaphthalen-1-yl) acetate
InChI codeInChI=1S/C16H14F3N3OS/c1-10-13(23-9-16(17,18)19)7-8-20-14(10)15-21-11-5-3-4-6-12(11)22(15)24-2/h3-8H,9H2,1-2H3
InChI KeyRZSYMONMXLYBMJ-UHFFFAOYSA-N
SMILESCSn1c(-c2nccc(OCC(F)(F)F)c2C)nc2ccccc21

Other names (synonyms)

IUPAC nomenclature provides a standardized method for naming chemical compounds. Although this system is widely used in chemistry, many chemical compounds have also other names commonly used in different contexts. These synonyms can come from a variety of sources and are used for a variety of purposes.

One common source of synonyms for chemical compounds is the common or trivial names, assigned on the basis of appearance, properties, or origin of the molecule.

Another source of synonyms are historical or obsolete names employed in the past, however replaced nowadays by more modern or standardized names.

In addition to common and historical names, chemical compounds may also have synonyms that are specific to a particular field or industry.

  • (4-acetyloxy-2-methylnaphthalen-1-yl) acetate
  • (4-acetyloxy-3-methylnaphthalen-1-yl) acetate
  • 1, 2-methyl-, diacetate
  • 1, 4-Diacetoxy-2-methylnaphthalene
  • 1,4-Diacetoxy-2-methylnaphthalene
  • 1,4-Diacetoxy-3-methyl-naphthalin
  • 1,4-NAPHTHALENEDIOL, 2-METHYL-, DIACETATE
  • 1,4-Naphthalenediol,2-methyl-,diacetate
  • 2-Methyl-1,4-naphthalenediol diacetate
  • 2-Methyl-1,4-naphthohydroquinone diacetate
  • 2-Methyl-1,4-naphthoquinol diacetate
  • 2-Methyl-1,4-naphthylene diacetate
  • 2-Methylnaphthalene-1,4-diyl diacetate
  • 2-Methylnaphthalene-1,4-diyldiacetate
  • 4-(Acetyloxy)-2-methyl-1-naphthyl acetate
  • 4-(Acetyloxy)-2-methyl-1-naphthyl acetate #
  • 4-(acetyloxy)-2-methylnaphthalen-1-yl acetate
  • 573-20-6
  • A831392
  • AS-12656
  • Acetomenadione
  • Acetomenaphthone
  • Acetomenaphthone (Menadiol Diacetate)
  • Acetomenaphthone, BAN
  • Acetomenaphtone
  • Acetomenaphtone (JAN)
  • Adaprin
  • BRN 1991457
  • CCG-267042
  • CS-8181
  • D01676
  • D84089
  • DSSTox_CID_26236
  • DSSTox_GSID_46236
  • DSSTox_RID_81463
  • DWG8UZD9HT
  • Davitamon-K
  • Davitamon-K-oral
  • FT-0632415
  • HY-B1508
  • Kapathrom
  • Kapilin
  • Kapilon
  • Kativ powder
  • Kayvite
  • MFCD00021469
  • MLS004773967
  • MLS006010226
  • Menadiol Acetate,(S)
  • Menadiol di(acetate)
  • Menadiol diacetate
  • NCGC00160567-01
  • NSC 403062
  • NSC-403062
  • NSC403062
  • Pafavit
  • Prokayvit oral
  • Q-200582
  • Q27276648
  • RYWSYCQQUDFMAU-UHFFFAOYSA-
  • SMR001550632
  • SR-01000883680
  • SR-01000883680-1
  • V0103
  • Vitamin K diacetate
  • Vitamin K4
  • Vitavel K
  • WLN: L66J BOV1 C1 EOV1
  • s4779

Reference codes for other databases

There exist several different chemical codes commonly used in orded to identify molecules:
  • ZINC867
  • CAS-573-20-6
  • UNII-DWG8UZD9HT
  • AKOS015907780
  • DTXSID4046236
  • CHEMBL1479848
  • CHEBI:31164
  • Tox21_111905
  • EINECS 209-352-1
  • SCHEMBL209382

Physico-Chemical properties

IUPAC name(4-acetyloxy-3-methylnaphthalen-1-yl) acetate
Molecular formulaC16H14F3N3OS
Molecular weight353.362
Melting point (ºC)
Boiling point (ºC)
Density (g/cm3)
Molar refractivity88.27
LogP4.5
Topological polar surface area65.2

LogP and topological polar surface area (TPSA) values were estimated using Open Babel software.

The n-octanol/water partition coeficient (Kow) data is applied in toxicology and drug research. Kow values are used, to guess the environmental fate of persistent organic pollutants. High partition coefficients values, tend to accumulate in the fatty tissue of organisms. Molecules with a log(Kow) (or LogP) greater than 5 are considered to bioaccumulate.

TPSA values are the sum of the surface area over all polar atoms or molecules, mainly oxygen and nitrogen, also including hydrogen atoms.

In medicinal chemistry, TPSA is used to assess the ability of a drug to permeabilise cells.

For molecules to penetrate the blood-brain barrier (and act on receptors in the central nervous system), TPSA values below 90 Å2 are required. Thus, molecules with a polar surface area greater than 140 Å2 tend to be poorly permeable to cell membranes.