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ChemicalBook--->CAS DataBase List--->13241-32-2

13241-32-2

13241-32-2 Structure

13241-32-2 Structure
IdentificationBack Directory
[Name]

NEOERIOCITRIN
[CAS]

13241-32-2
[Synonyms]

C09805
NEOERIOCITRIN
NEOERIOCITRIN WITH HPLC
ERIODICTYOL-7-NEOHESPERIDOSIDE
ERIODICTYOL-7-O-NEOHESPERIDOSIDE
Neoeriocitrin, froM Citrus nobilis
ERIODICTYOL-7-NEOHESPERIDOSIDE hplc
(s)-3',4',5,7-tetrahydroxyflavanone-7-[2-o-(α-l-rhamnopyranosyl)-β-d-glucopyranoside]
(S)-3',4',5,7-TETRAHYDROXYFLAVANONE-7-[2-O-(ALPHA-L-RHAMNOPYRANOSYL)-BETA-D-GLUCOPYRANOSIDE]
(S)-7-[[2-O-(6-Deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-2-(3,4-dihydroxyphenyl)-2,3-dihydro-5-hydroxy-4H-1-benzopyran-4-one
4H-1-Benzopyran-4-one,7-[[2-O-(6-deoxy-a-L-mannopyranosyl)-b-D-glucopyranosyl]oxy]-2-(3,4-dihydroxyphenyl)-2,3-dihydro-5-hydroxy-,(2S)-
4H-1-Benzopyran-4-one, 7-[[2-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-2-(3,4-dihydroxyphenyl)-2,3-dihydro-5-hydroxy-, (2S)-
(S)-7-[[2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl]oxy]-2-(3,4-dihydroxyphenyl)-2,3-dihydro-5-hydroxy-4H-benzopyran-4-one
7-[[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyl-2-oxanyl)oxy]-2-oxanyl]oxy]-2-(3,4-dihydroxyphenyl)-5-hydroxy-3,4-dihydro-2H-1-benzopyran-4-one
[EINECS(EC#)]

236-215-3
[Molecular Formula]

C27H32O15
[MDL Number]

MFCD00017474
[MOL File]

13241-32-2.mol
[Molecular Weight]

596.53
Chemical PropertiesBack Directory
[Melting point ]

277°C
[Boiling point ]

960.7±65.0 °C(Predicted)
[density ]

1.73±0.1 g/cm3 (20 ºC 760 Torr)
[storage temp. ]

Store at -20°C
[solubility ]

Soluble in methanol;
[form ]

powder
[pka]

7.14±0.40(Predicted)
[color ]

White
[Water Solubility ]

insoluble in water
[BRN ]

1696764
[LogP]

2.130 (est)
Safety DataBack Directory
[WGK Germany ]

3
[F ]

10-21
[HS Code ]

29389090
Hazard InformationBack Directory
[Chemical Properties]

Off white powder
[Definition]

ChEBI: A flavanone glycoside that is eriodictyol substituted by a 2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl residue at position 7 via a glycosidic linkage.
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