Cas 95541-48-3,(3R,4S,2'R,3'S)-2'-(3,4-Dihydroxy-phenyl)-3-(2-hydroxy-4-methoxy-phenyl)-7-methoxy-3,4,3',4'-tetrahydro-2H,2'H-[4,6']bichromenyl-3',5',7'-triol

95541-48-3

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Basic information

Product Name: (3R,4S,2'R,3'S)-2'-(3,4-Dihydroxy-phenyl)-3-(2-hydroxy-4-methoxy-phenyl)-7-methoxy-3,4,3',4'-tetrahydro-2H,2'H-[4,6']bichromenyl-3',5',7'-triol
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CAS NO:95541-48-3
Molecular Formula:
Molecular Weight: 574.584
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (3R,4S,2'R,3'S)-2'-(3,4-Dihydroxy-phenyl)-3-(2-hydroxy-4-methoxy-phenyl)-7-methoxy-3,4,3',4'-tetrahydro-2H,2'H-[4,6']bichromenyl-3',5',7'-triol(CAS DataBase Reference)
NIST Chemistry Reference: (3R,4S,2'R,3'S)-2'-(3,4-Dihydroxy-phenyl)-3-(2-hydroxy-4-methoxy-phenyl)-7-methoxy-3,4,3',4'-tetrahydro-2H,2'H-[4,6']bichromenyl-3',5',7'-triol(95541-48-3)
EPA Substance Registry System: (3R,4S,2'R,3'S)-2'-(3,4-Dihydroxy-phenyl)-3-(2-hydroxy-4-methoxy-phenyl)-7-methoxy-3,4,3',4'-tetrahydro-2H,2'H-[4,6']bichromenyl-3',5',7'-triol(95541-48-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 95541-48-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 95541-48-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,5,4 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 95541-48:
(7*9)+(6*5)+(5*5)+(4*4)+(3*1)+(2*4)+(1*8)=153
153 % 10 = 3
So 95541-48-3 is a valid CAS Registry Number.

95541-48-3Upstream product

95541-48-3Downstream Products

95541-50-7 (3R,4S)-3,4-trans-4-<(2R,3S)-2,3-trans-3-acetoxy-3',4',5,7-tetramethoxyflavan-6-yl>-2',3',7-trimethoxyisoflavan

95541-48-3Relevant academic research and scientific papers

Synthesis of Isoflavanoid Oligomers Using a Pterocarpan as Inceptive Electrophile

Bezuidenhoudt, Barend C. B.,Brandt, Edward V.,Roux, David G.

, p. 2767 - 2778 (2007/10/02)

(3S)-2',7-Dihydroxy-4'-methoxyisoflavan serves as bifunctional nucleophile at C-5' and C-6, when condensed with the carbocation generated at C-11a of its (6aS,11aS)-3-hydroxy-9-methoxypterocarpan analogue under mild acid conditions or by photolysis, to fo

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