Home > Compound List > Compound details
4940-39-0 molecular structure
click picture or here to close

4-oxo-4H-chromene-2-carboxylic acid

ChemBase ID: 70597
Molecular Formular: C10H6O4
Molecular Mass: 190.15224
Monoisotopic Mass: 190.02660867
SMILES and InChIs

SMILES:
c1(cc(=O)c2ccccc2o1)C(=O)O
Canonical SMILES:
OC(=O)c1cc(=O)c2c(o1)cccc2
InChI:
InChI=1S/C10H6O4/c11-7-5-9(10(12)13)14-8-4-2-1-3-6(7)8/h1-5H,(H,12,13)
InChIKey:
RVMGXWBCQGAWBR-UHFFFAOYSA-N

Cite this record

CBID:70597 http://www.chembase.cn/molecule-70597.html

Collapse All Expand All

NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
4-oxo-4H-chromene-2-carboxylic acid
IUPAC Traditional name
chromone-2-carboxylic acid
4-oxo-4H-chromene-2-carboxylic acid
Synonyms
4-Oxo-4H-1-benzopyran-2-carboxylic acid
4-Oxo-4H-1-Benzopyran-2-carboxylic acid
Chromocarb
Chromocarb
4-Oxo-4H-chromene-2-carboxylic acid
Chromone-2-carboxylic acid
4-Oxo-4H-1-benzopyran-2-carboxylic acid
Chromone-2-carboxylic acid
Chromone-2-carboxylic acid
Atremon
Chromocarb
4-氧代-4H-1-苯并吡喃-2-羧酸
色烯卡
色酮-2-羧酸
4-氧代-4H-1-苯并吡喃-2-羧酸
二氢色原酮-2-甲酸
CAS Number
4940-39-0
EC Number
225-583-0
MDL Number
MFCD00006838
Beilstein Number
146442
Merck Index
142237
PubChem SID
24898061
162036312
24851396
PubChem CID
2741

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 2.2516267  H Acceptors
H Donor LogD (pH = 5.5) -1.7904763 
LogD (pH = 7.4) -2.2228043  Log P 1.2971071 
Molar Refractivity 48.5934 cm3 Polarizability 18.022148 Å3
Polar Surface Area 63.6 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Pharmacology Properties Product Information Bioassay(PubChem)
Melting Point
257 - 259°C expand Show data source
260 °C (dec.)(lit.) expand Show data source
260(dec.)°C expand Show data source
ca 260°C dec. expand Show data source
Hydrophobicity(logP)
1.3 expand Show data source
Storage Warning
IRRITANT expand Show data source
Irritant expand Show data source
RTECS
DJ2476000 expand Show data source
European Hazard Symbols
Irritant Irritant (Xi) expand Show data source
MSDS Link
Download expand Show data source
Download expand Show data source
Download expand Show data source
German water hazard class
3 expand Show data source
Risk Statements
36/37/38 expand Show data source
Safety Statements
26-36 expand Show data source
26-37 expand Show data source
TSCA Listed
false expand Show data source
expand Show data source
GHS Pictograms
GHS07 expand Show data source
GHS Signal Word
Warning expand Show data source
GHS Hazard statements
H315-H319-H335 expand Show data source
GHS Precautionary statements
P261-P305 + P351 + P338 expand Show data source
P261-P305+P351+P338-P302+P352-P321-P405-P501A expand Show data source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves expand Show data source
Target
Others expand Show data source
Gene Information
human ... PTPN1(5770) expand Show data source
Purity
95% expand Show data source
95+% expand Show data source
97% expand Show data source
Salt Data
Free Bse expand Show data source
Certificate of Analysis
Download expand Show data source
Application(s)
Sedative expand Show data source
Spasmolytic agent expand Show data source
Empirical Formula (Hill Notation)
C10H6O4 expand Show data source

DETAILS

DETAILS

MP Biomedicals MP Biomedicals Sigma Aldrich Sigma Aldrich
MP Biomedicals - 02156018 external link
(Chromocarb; Chromone-2-carboxylic acid)
Sigma Aldrich - 189782 external link
Packaging
5 g in glass bottle

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • • Aldrich Library of 13C and 1H FT NMR Spectra, 1992, 2, 1176C, (nmr)
  • • Aldrich Library of FT-IR Spectra, 1st edn., 1985, 2, 245C, (ir)
  • • Ruhemann, S. et al., J.C.S., 1900, 77, 1179; 1901, 79, 470, (synth)
  • • Zagorevskii, V.A. et al., Zh. Obshch. Khim., 1963, 33, 2469; Chem. Heterocycl. Compd. (Engl. Transl.), 1967, 3, 786, (synth)
  • • Tronche, P. et al., Ann. Pharm. Fr., 1965, 23, 573, (derivs)
  • • Barker, G. et al., Org. Mass Spectrom., 1971, 5, 857, (ms)
  • • Griffiths, P.J.F. et al., Spectrochim. Acta A, 1972, 28, 707, (uv)
  • • Ellis, G.P. et al., Prog. Med. Chem., 1973, 9, 65, (rev)
  • • Neuman, M., Drugs of Today (Barcelona), 1977, 13, 359, (rev, pharmacol)
  • • Bevan, P.S. et al., J.C.S. Perkin 1, 1981, 9, 2552, (synth, derivs)
  • • Payard, M. et al., Eur. J. Med. Chem. (Chim. Ther.), 1985, 20, 117, (synth, activity)
  • • Smith, D.A. et al., Drug Metab. Rev., 1986, 16, 365, (rev, metab)
  • • Martindale, The Extra Pharmacopoeia, 30th edn., Pharmaceutical Press, 1993, 1352
  • Searching...Please wait...

PATENTS

PATENTS

PubChem iconPubChem Patent Google Patent Search IconGoogle Patent

INTERNET

INTERNET

Baidu iconBaidu google iconGoogle