Cas 85915-65-7,(3S,4S)-3,4-trans-4-<(3S)-2',7-dihydroxy-4'-methoxyisoflavan-6-yl>-2',7-dihydroxy-4'-methoxyisoflavan

85915-65-7

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Basic information

Product Name: (3S,4S)-3,4-trans-4-<(3S)-2',7-dihydroxy-4'-methoxyisoflavan-6-yl>-2',7-dihydroxy-4'-methoxyisoflavan
Synonyms:
CAS NO:85915-65-7
Molecular Formula:
Molecular Weight: 542.585
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: (3S,4S)-3,4-trans-4-<(3S)-2',7-dihydroxy-4'-methoxyisoflavan-6-yl>-2',7-dihydroxy-4'-methoxyisoflavan(CAS DataBase Reference)
NIST Chemistry Reference: (3S,4S)-3,4-trans-4-<(3S)-2',7-dihydroxy-4'-methoxyisoflavan-6-yl>-2',7-dihydroxy-4'-methoxyisoflavan(85915-65-7)
EPA Substance Registry System: (3S,4S)-3,4-trans-4-<(3S)-2',7-dihydroxy-4'-methoxyisoflavan-6-yl>-2',7-dihydroxy-4'-methoxyisoflavan(85915-65-7)

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: 85915-65-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 85915-65-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,9,1 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 85915-65:
(7*8)+(6*5)+(5*9)+(4*1)+(3*5)+(2*6)+(1*5)=167
167 % 10 = 7
So 85915-65-7 is a valid CAS Registry Number.

85915-65-7Upstream product

85915-65-7Downstream Products

85929-32-4 (3S,4S)-3,4-trans-2',4',7-trimethoxy-4-<(3S)-3',4',7-trimethoxyisoflavan-6-yl>isoflavan

85915-65-7Relevant 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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