105655-99-0 Usage
Uses
Used in Pharmaceutical Industry:
(5R-(5alpha,5abeta,8aalpha,9beta))-9-((2-Deoxy-2-(dimethylamino)-4,6-O-ethylidene-beta-D-glucopyranosyl)oxy)-5,8,8a,9-tetrahydro-5-(4-hydroxy-3,5-dimethoxyphenyl)furo[3',4':6,7]naphtho[2,3-d]-1,3-dioxol-6(5aH)-one is used as a potential pharmaceutical compound for its unique structure and possible biological activities, which may contribute to the development of new drugs and therapies.
Used in Research and Development:
In the field of organic chemistry and medicinal chemistry, (5R-(5alpha,5abeta,8aalpha,9beta))-9-((2-Deoxy-2-(dimethylamino)-4,6-O-ethylidene-beta-D-glucopyranosyl)oxy)-5,8,8a,9-tetrahydro-5-(4-hydroxy-3,5-dimethoxyphenyl)furo[3',4':6,7]naphtho[2,3-d]-1,3-dioxol-6(5aH)-one serves as a subject for research and development, allowing scientists to explore its properties, potential applications, and interactions with biological systems. Its unique structure may provide insights into the design of new molecules with specific therapeutic effects.
Used in Natural Product Chemistry:
As a natural product found in plants, (5R-(5alpha,5abeta,8aalpha,9beta))-9-((2-Deoxy-2-(dimethylamino)-4,6-O-ethylidene-beta-D-glucopyranosyl)oxy)-5,8,8a,9-tetrahydro-5-(4-hydroxy-3,5-dimethoxyphenyl)furo[3',4':6,7]naphtho[2,3-d]-1,3-dioxol-6(5aH)-one is used in the study of natural product chemistry to understand its role in plants and its potential applications in various industries, such as pharmaceuticals, cosmetics, and agriculture.
Check Digit Verification of cas no
The CAS Registry Mumber 105655-99-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,6,5 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 105655-99:
(8*1)+(7*0)+(6*5)+(5*6)+(4*5)+(3*5)+(2*9)+(1*9)=130
130 % 10 = 0
So 105655-99-0 is a valid CAS Registry Number.
105655-99-0Relevant articles and documents
The Catalytically Lignan-Activation-Based Approach for the Synthesis of (epi)-Podophyllotoxin Derivatives
Wan, Jun-Hao,Hu, Yang,Liu, Hui,Tu, Yuan-Hong,He, Zhong-Yi,Sun, Jian-Song
, p. 5652 - 5662 (2017/06/07)
Under the effect of a catalytic amount of Au(I) complex, 4-O-(2-cyclopropylethynyl)benzoyl-(epi)-podophyllotoxins, easily prepared via dehydrative condensation between (epi)-podophyllotoxin and ortho-cyclopropylethynylbenzoic acid, could efficiently coupl
Preparation method of podophyllotoxin 4-OH derivative
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Paragraph 0099-0101; 0125-0128, (2017/08/29)
The invention provides a preparation method of a podophyllotoxin 4-OH derivative. A podophyllotoxin 4-OH derivative 1 shown in the specification can be prepared from a compound 2 and a compound 3 through glycosylation , wherein R1 is a common hydroxyl pro
Etoposide: a new approach to the synthesis of 4-O-(2-amino-2-deoxy-4,6-O-ethylidene-β-D-glucopyranosyl)-4'-O-demethyl-4-epipodophyllotoxin
Kolar, Cenek,Dehmel, Konrad,Wolf, Heinz
, p. 219 - 231 (2007/10/02)
Synthesis of 3-O-acetyl-2-benzyloxycarbonylamino-2-deoxy-4,6-O-ethylidene-α-(7α) and -β-D-glucopyranose (7β) and their 3-O-chloroacetyl analogues (11α and 11β) are described.Condensation (BF3-etherate, ethyl acetate, -20 deg C) of 7α with 4'-O-benzyloxyca
Syntheses of All Four Possible Diastereomers of Etoposide and Its Aminoglycosidic Analogues via Optical Resolution of (+/-)-Podophyllotoxin by Glycosidation with D- and L-Sugars
Saito, Hitoshi,Nishimura, Yoshio,Kondo, Shinichi,Umezawa, Hamao
, p. 799 - 802 (2007/10/02)
Syntheses of all four possible diastereomers of etoposide and its aminoglycosidic analogues have been achieved via optical resolution of (+/-)-podophyllotoxin by glycosidation with D- and L-sugars.
