MDL | MFCD00020256 |
InChIKey | FRMWBRPWYBNAFB-UHFFFAOYSA-M |
Inchi | InChI=1S/C7H6O3.K/c8-6-4-2-1-3-5(6)7(9)10;/h1-4,8H,(H,9,10);/q;+1/p-1 |
SMILES | C([O-])(=O)C1=CC=CC=C1O.[K+] |
LogP | -0.24430 |
PSA | 60.36000 |
熔点 | 249-255°C |
精确分子量 | 175.98800 |
EINECS | 209-421-6 |
1.
Index of subjects
J. Chem. Soc. Abstr. 1910 98 ii1267
2.
A critical review of the production of hydroxyaromatic carboxylic acids as a sustainable method for chemical utilisation and fixation of CO2
Omar Mohammad,Jude A. Onwudili,Qingchun Yuan RSC Sustain. 2023 1 404
3.
CCCX.—Use of the salts of the arylsulphonhalogenoamides in the estimation and iodination of phenols
Elwyn Roberts J. Chem. Soc. Trans. 1923 123 2707
4.
Comparison of complex formation by thallium(I) and potassium salts of potentially chelating anions
N. S. Poonia,Mary R. Truter J. Chem. Soc. Dalton Trans. 1972 1791
5.
128. Conductimetric studies in ketonic solvents. Part III. Alkali iodides and salicylates in ethyl methyl ketone and acetophenone
S. R. C. Hughes J. Chem. Soc. 1957 634
6.
639. Mechanism of the Kolbe–Schmitt reaction. Part II. Influence of the alkali metal
S. E. Hunt,J. Idris Jones,A. S. Lindsey,D. C. Killoh,H. S. Turner J. Chem. Soc. 1958 3152
7.
Thermodynamic and kinetic implications involved in the titration of polyfunctional acids by catalytic thermometric titrimetry
Oswaldo E. S. Godinho,Helena S. Nakatani,Ivo M. Raimundo,Luiz M. Aleixo,Graciliano de Oliveira Neto Analyst 1991 116 947
8.
Carboxylations of alkali metal phenoxides with carbon dioxide
Yoshio Kosugi,Yoshio Imaoka,Fumisato Gotoh,Mohammad A. Rahim,Yoshihisa Matsui,Kinya Sakanishi Org. Biomol. Chem. 2003 1 817
9.
The diffusion potentials and ionic mobilities of benzoates and salicylates, and their modification by a membrane of parchment paper
Edmund Brydges Rudhall Prideaux,William Ernest Crooks Trans. Faraday Soc. 1924 20 37
10.
296. The electrical conductivity of uni-univalent salts in acetone
J. F. J. Dippy,H. O. Jenkins,J. E. Page J. Chem. Soc. 1939 1386
PubChemId | 23664627 |
SMILES
[K+].O=C([O-])C1C(O)=CC=CC=1