2-Biphenylcarboxylic acid
2-Biphenylcarboxylic acid
  • CAS No.:947-84-2
Other grades of this product :
2-Biphenylcarboxylic acid Basic information
Product Name:2-Biphenylcarboxylic acid
Synonyms:O-PHENYLBENZOIC ACID;TIMTEC-BB SBB007790;RARECHEM AL BE 0859;[1,1’-Biphenyl]-2-carboxylicacid;LABOTEST-BB LT0;2-Biphenylcarboxylic acid2;-Methoxyphenyl)proanol-methyl-d3;-Aminobenzyl)thio]cellobiose
CAS:947-84-2
MF:C13H10O2
MW:198.22
EINECS:213-432-1
Product Categories:Biphenyl series;Biphenyl derivatives;Benzene derivatives;Organic acids
Mol File:947-84-2.mol
2-Biphenylcarboxylic acid Chemical Properties
Melting point 111-113 °C(lit.)
Boiling point 199 °C10 mm Hg(lit.)
density 1.1184 (rough estimate)
refractive index 1.5954 (estimate)
Fp 343-344°C
storage temp. Sealed in dry,Room Temperature
form Crystalline Powder
pka3.46(at 25℃)
color White to beige
Water Solubility insoluble
BRN 974075
InChIKeyILYSAKHOYBPSPC-UHFFFAOYSA-N
CAS DataBase Reference947-84-2(CAS DataBase Reference)
NIST Chemistry Reference2-Biphenylcarboxylic acid(947-84-2)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36-37/39-37
WGK Germany 3
HazardClass IRRITANT
HS Code 29163900
MSDS Information
ProviderLanguage
2-Phenylbenzoic acid English
ACROS English
SigmaAldrich English
ALFA English
2-Biphenylcarboxylic acid Usage And Synthesis
Chemical Properties2-Biphenylcarboxylic acid is White powder
Uses2-Biphenylcarboxylic acid is used in the preparation of neuropeptide FF receptor antagonists. In addition it is used in the synthesis of disubstituted piperidines as orexin receptor antagonists.
UsesIt is used as a pharmaceutical intermediate. he reaction of 2?-substituted biphenyl-2-carboxylic acids (where the 2?-substituent is H, CO2H, NO2, Cl, OMe, or CO2Me) with lead tetra-acetate in refluxing benzene solution, under a nitrogen atmosphere, affords 3,4-benzocoumarin as a major organic product.
Synthesis Reference(s)The Journal of Organic Chemistry, 43, p. 447, 1978 DOI: 10.1021/jo00397a015
Purification MethodsCrystallise the acid from *C6H6/pet ether or aqueous EtOH. [Beilstein 9 IV 2472.]

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