107585-77-3 Usage
Description
4'-Demethyl-3,9-dihydroeucomin is a chemical compound belonging to the class of organic compounds known as indolizidines. Indolizidines are polycyclic compounds characterized by an indolizidine moiety, which consists of a bicyclic system with a three-membered ring and a pyrrole fused together. Although specific information about the properties, uses, and potential hazards of 4'-Demethyl-3,9-dihydroeucomin is limited, it is likely to share some characteristics common to indolizidines due to its structure.
Uses
Due to the limited information available on 4'-Demethyl-3,9-dihydroeucomin, its specific applications are not well-documented. However, based on its classification as an indolizidine, it may have potential uses in various industries, such as:
Used in Pharmaceutical Industry:
4'-Demethyl-3,9-dihydroeucomin could be used as a pharmaceutical compound for [application reason], given its indolizidine structure, which may offer specific biological activities or therapeutic properties.
Used in Chemical Research:
In the field of chemical research, 4'-Demethyl-3,9-dihydroeucomin may serve as a subject of study for understanding the properties and behavior of indolizidines, contributing to the development of new compounds or applications.
Used in Material Science:
4'-Demethyl-3,9-dihydroeucomin might be utilized in material science for [application reason], potentially due to its structural features that could influence its physical or chemical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 107585-77-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,5,8 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 107585-77:
(8*1)+(7*0)+(6*7)+(5*5)+(4*8)+(3*5)+(2*7)+(1*7)=143
143 % 10 = 3
So 107585-77-3 is a valid CAS Registry Number.
107585-77-3Relevant articles and documents
Chemistry of Homoisoflavonoids: Synthesis of Polyhydroxy 3-Benzylchromones and 3-Benzylchroman-4-ones without Protection and Deprotection of Hydroxyl Groups and a Convenient Preparation of Benzylidenechroman-4-ones
Sathyanarayana, S.,Krishnamurty, H. G.
, p. 899 - 901 (2007/10/02)
Catalytic transfer hydrogenation of hydroxyflavanones gives hydroxydihydrochalcones.These dihydrochalcones are converted into hydroxyhomoisoflavones and homoisoflavanones without protection and deprotection of hydroxyl groups.The condensation between chromanones and aryl aldehydes in the presence of dry p-toluenesulfonic acid in benzene or toluene gives benzylidenechromanones in good yields.The method is far superior to all other existing procedures.
