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548-77-6

Basic Information
CAS No.: 548-77-6
Name: Tectorigenin
Article Data: 10
Molecular Structure:
Molecular Structure of 548-77-6 (Tectorigenin)
Formula: C16H12O6
Molecular Weight: 300.268
Synonyms: Tectoridin;5-18-05-00311 (Beilstein Handbook Reference);Tectorigenine;5,7-dihydroxy-3-(4-hydroxyphenyl)-6-methoxy-chromen-4-one;4,5,7-Trihydroxy-6-methoxyisoflavone;K 251T;4H-1-Benzopyran-4-one,5,7-dihydroxy-3- (4-hydroxyphenyl)-6-methoxy-;
Density: 1.512 g/cm3
Melting Point: 225-226°
Boiling Point: 601.506 °C at 760 mmHg
Flash Point: 230.135 °C
PSA: 100.13000
LogP: 2.58540
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Specification

The Tectorigenin, with the CAS registry number 548-77-6, is also known as 4,5,7-Trihydroxy-6-methoxyisoflavone. This chemical's molecular formula is C16H12O6 and molecular weight is 300.26. What's more, its systematic name is 5,7-Dihydroxy-3-(4-hydroxyphenyl)-6-methoxy-4H-chromen-4-one. Its classification code is Mutation data. Tectorigenin is an O-methylated isoflavone, a type of flavonoid. It can be isolated from leopard lily (Belamcanda chinensis), in Iris unguicularis or Pueraria thunbergiana.

Physical properties of Tectorigenin are: (1)ACD/LogP: 2.838; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 2.78; (4)ACD/LogD (pH 7.4): 1.65; (5)ACD/BCF (pH 5.5): 74.05; (6)ACD/BCF (pH 7.4): 5.45; (7)ACD/KOC (pH 5.5): 730.25; (8)ACD/KOC (pH 7.4): 53.76; (9)#H bond acceptors: 6; (10)#H bond donors: 3; (11)#Freely Rotating Bonds: 5; (12)Polar Surface Area: 96.22 Å2; (13)Index of Refraction: 1.697; (14)Molar Refractivity: 76.53 cm3; (15)Molar Volume: 198.565 cm3; (16)Polarizability: 30.339×10-24cm3; (17)Surface Tension: 72.8 dyne/cm; (18)Density: 1.512 g/cm3; (19)Flash Point: 230.135 °C; (20)Enthalpy of Vaporization: 92.805 kJ/mol; (21)Boiling Point: 601.506 °C at 760 mmHg; (22)Vapour Pressure: 0 mmHg at 25°C.

Preparation of Tectorigenin: this chemical can be prepared by 5,7-dihydroxy-6-methoxy-3-(4-methoxy-phenyl)-chromen-4-one at the temperature of - 70 °C. This reaction will need reagent boron tribromide and solvent H2Cl2 with the reaction time of 3 hours. The yield is about 40%.

Tectorigenin can be prepared by 5,7-dihydroxy-6-methoxy-3-(4-methoxy-phenyl)-chromen-4-one at the temperature of - 70 °C

You can still convert the following datas into molecular structure:
(1)SMILES: O=C\1c3c(O)c(OC)c(O)cc3O/C=C/1c2ccc(O)cc2
(2)Std. InChI: InChI=1S/C16H12O6/c1-21-16-11(18)6-12-13(15(16)20)14(19)10(7-22-12)8-2-4-9(17)5-3-8/h2-7,17-18,20H,1H3
(3)Std. InChIKey: OBBCRPUNCUPUOS-UHFFFAOYSA-N

The toxicity data is as follows:  

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intraperitoneal 3gm/kg (3000mg/kg) BEHAVIORAL: ALTERED SLEEP TIME (INCLUDING CHANGE IN RIGHTING REFLEX)

LUNGS, THORAX, OR RESPIRATION: DYSPNEA

BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)
Nippon Yakurigaku Zasshi. Japanese Journal of Pharmacology. Vol. 64, Pg. 186, 1968.