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Chinese factory supply Morin 480-16-0 in stock with high standard
- Molecular Formula: C15H10O7
- Molecular Weight: 302.24
- Appearance/Colour: yellow to brown powder
- Vapor Pressure: 2.94E-17mmHg at 25°C
- Melting Point: 299-300 °C (dec.)(lit.)
- Refractive Index: 1.823
- Boiling Point: 645.5 °C at 760 mmHg
- PKA: 6.30±0.40(Predicted)
- Flash Point: 249.3 °C
- PSA： 131.36000
- Density: 1.799 g/cm3
- LogP: 1.98800
Morin(Cas 480-16-0) Usage
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Safety Profile |
Moderately toxic by intraperitoneal route. Mutation data reported. When heated to decomposition it emits acrid smoke and irritating fumes. |
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Purification Methods |
Stir morin at room temperature with ten times its weight of absolute EtOH, then leave overnight to settle. Filter it off, and evaporate under a heat lamp to one-tenth its volume. An equal volume of water is added, and the precipitated morin is filtered off, dissolved in the minimum amount of EtOH and again precipitated with an equal volume of water. The precipitate is filtered off, washed with water and dried at 110o for 1hour (yield ca 2.5%.). [Perkins & Kalkwarf Anal Chem 28 1989 1956.] It complexes with W and Zr. [Beilstein 18 H 239, 18 III/IV 3468, 18/5 V 492.] |
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Definition |
ChEBI: A pentahydroxyflavone that is 7-hydroxyflavonol bearing three additional hydroxy substituents at positions 2' 4' and 5. |
InChI:InChI=1/C15H10O7/c16-6-1-2-8(9(18)3-6)15-14(21)13(20)12-10(19)4-7(17)5-11(12)22-15/h1-5,16-19,21H
480-16-0 Relevant articles
SYNTHESIS OF MORIN AND MORIN DERIVATIVES
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Paragraph 0039, (2020/11/24)
The invention relates to a method for di...
The total synthesis of (±)-sanggenol F
Sheng, Xiao,Jia, Xin-Yu,Tang, Fei,Wang, Yang,Hou, Ai-Jun
, p. 3485 - 3491 (2017/06/01)
A concise and efficient total synthesis ...
Pharmacophore and docking-based hierarchical virtual screening for the designing of aldose reductase inhibitors: Synthesis and biological evaluation
Vyas, Bhawna,Singh, Manjinder,Kaur, Maninder,Silakari, Om,Bahia, Malkeet Singh,Singh, Baldev
, p. 609 - 626 (2016/03/08)
A set of 54 studied flavonoid inhibitors...
Flavonol glycosides from muehlenbeckia platyclada and their anti-inflammatory activity
Yen, Chiao-Ting,Hsieh, Pei-Wen,Hwang, Tsong-Long,Lan, Yu-Hsuan,Chang, Fang-Rong,Yang-Chang
experimental part, p. 280 - 282 (2009/10/15)
A new flavonol, morin-3-O-α-rhamnopyrano...
480-16-0 Process route
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1173997-99-3
morin 3-O-α-L-rhamnopyranoside
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3615-41-6,478518-52-4
L-Rhamnose
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-
480-16-0
morin
Conditions
| Conditions | Yield |
|---|---|
|
With
hydrogenchloride; water;
at 85 ℃;
for 2h;
|
-
-
84757-50-6
2-(2,4-dimethoxyphenyl)-3-hydroxy-5,7-dimethoxy-4H-chromen-4-one
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-
480-16-0
morin
Conditions
| Conditions | Yield |
|---|---|
|
With
pyridine hydrochloride;
at 220 ℃;
for 0.25h;
Sealed tube;
|
93%
|
|
With
hydrogen bromide; acetic acid;
In
water;
for 24h;
Inert atmosphere;
Reflux;
|
65%
|
480-16-0 Upstream products
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1173997-99-3
morin 3-O-α-L-rhamnopyranoside
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480-66-0
2,4,6-trihydroxyacetophenone
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95-01-2
2,4-Dihydroxybenzaldehyde
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84757-50-6
2-(2,4-dimethoxyphenyl)-3-hydroxy-5,7-dimethoxy-4H-chromen-4-one
480-16-0 Downstream products
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7555-80-8
pentamethyl morin
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79400-75-2
morin-5'-sulfonic acid
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89-86-1
4-hydroxysalicylic acid
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144-62-7
oxalic acid
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