60102-29-6 Usage
Uses
Used in Pharmaceutical Industry:
2-[(R)-3,4-Dihydro-7-methoxy-2H-1-benzopyran-3-yl]-5-methoxyphenol is used as a potential pharmaceutical compound for its potential involvement in various chemical reactions and interactions. The complex molecular structure of this organic compound may offer unique properties that could be harnessed for the development of new drugs or therapeutic agents.
Used in Chemical Research:
2-[(R)-3,4-Dihydro-7-methoxy-2H-1-benzopyran-3-yl]-5-methoxyphenol is used as a subject of study in chemical research to explore its reactivity, solubility, and other properties. Understanding these characteristics can provide insights into how 2-[(R)-3,4-Dihydro-7-methoxy-2H-1-benzopyran-3-yl]-5-methoxyphenol might be synthesized, modified, or utilized in various applications, including but not limited to the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 60102-29-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,1,0 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 60102-29:
(7*6)+(6*0)+(5*1)+(4*0)+(3*2)+(2*2)+(1*9)=66
66 % 10 = 6
So 60102-29-6 is a valid CAS Registry Number.
60102-29-6Relevant academic research and scientific papers
A general asymmetric route to enantio-enriched isoflavanes via an organocatalytic annulation of o-quinone methides and aldehydes
Zhang, Jian,Zhang, Shuangzhan,Yang, Huixin,Zhou, Ding,Yu, Xueting,Wang, Wei,Xie, Hexin
supporting information, p. 2407 - 2411 (2018/05/24)
Reported herein is a general approach to optically active isoflavanes based on a chiral amine-catalyzed [4 + 2] asymmetric annulation of o-quinone methides and aldehydes. A number of naturally occurring isoflavanes, including equol, sativan, isosativan, v
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
