49855-12-1 Usage
Uses
Used in Pharmaceutical Industry:
[1]Benzopyrano[3,4-b][1]benzopyran-12(6H)-one, 6a,12a-dihydro-9-hydroxy-2,3-dimethoxy-8-(3-methyl-2-butenyl)-, cisis used as a potential pharmaceutical compound for its unique molecular structure and properties. [1]Benzopyrano[3,4-b][1]benzopyran-12(6H)-one,
6a,12a-dihydro-9-hydroxy-2,3-dimethoxy-8-(3-methyl-2-butenyl)-, cis-'s specific functional groups and stereochemistry may allow it to interact with biological targets in novel ways, potentially leading to the development of new drugs for various medical conditions.
Used in Agrochemical Industry:
In the agrochemical industry, [1]Benzopyrano[3,4-b][1]benzopyran-12(6H)-one, 6a,12a-dihydro-9-hydroxy-2,3-dimethoxy-8-(3-methyl-2-butenyl)-, cismay be utilized as a starting material or intermediate in the synthesis of new agrochemicals. Its unique structure could provide novel modes of action or selectivity for pest control, crop protection, or other agricultural applications.
Used in Chemical Research:
[1]Benzopyrano[3,4-b][1]benzopyran-12(6H)-one, 6a,12a-dihydro-9-hydroxy-2,3-dimethoxy-8-(3-methyl-2-butenyl)-, ciscan also be used in chemical research as a model compound for studying the properties and reactivity of complex organic molecules. Its unique structure may provide insights into new reaction mechanisms, synthetic strategies, or the development of new catalysts and reagents for organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 49855-12-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,8,5 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 49855-12:
(7*4)+(6*9)+(5*8)+(4*5)+(3*5)+(2*1)+(1*2)=161
161 % 10 = 1
So 49855-12-1 is a valid CAS Registry Number.
49855-12-1Relevant academic research and scientific papers
The Stereospecific Generation of Chirally Labelled Benzylic Centres in o-Prenylphenols: 1'-R- and 1'-S-3H>-Rotenonic Acid
Bhandari, Prabha,Crombie, Leslie,Harper, Mark H.,Sanders, M.,Whiting, Donald A.
, p. 981 - 982 (2007/10/02)
The problem of generating rot-2'-enonic acid stereospecifically with tritium in the 1'-R- and 1'-S-benzylic positions of the prenyl group is solved by a method generally applicable to o-prenylphenols: chiral centres are constructed on a ring system, with
