4335-12-0 Usage
Uses
Used in Pharmaceutical Industry:
6-(3-Methyl-2-butenyl)-5,7-dimethoxy-2H-1-benzopyran-2-one is used as a pharmaceutical compound for its potential antioxidant and anti-inflammatory effects. Its presence in certain plants and natural products suggests that it may play a role in their biological activities, making it a promising candidate for the development of new drugs and therapies.
Used in Research and Development:
6-(3-Methyl-2-butenyl)-5,7-dimethoxy-2H-1-benzopyran-2-one is used as a subject of research in various fields, including medicine and agriculture. Its unique chemical structure and pharmacological properties make it an interesting target for further investigation to explore its potential applications and benefits in these industries.
Used in Natural Products:
6-(3-Methyl-2-butenyl)-5,7-dimethoxy-2H-1-benzopyran-2-one is found in certain plants and natural products, where it may contribute to their biological activities. Its presence in these sources highlights its potential use in the development of natural remedies and supplements that leverage its antioxidant and anti-inflammatory properties.
Check Digit Verification of cas no
The CAS Registry Mumber 4335-12-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,3 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4335-12:
(6*4)+(5*3)+(4*3)+(3*5)+(2*1)+(1*2)=70
70 % 10 = 0
So 4335-12-0 is a valid CAS Registry Number.
InChI:InChI=1/C16H18O4/c1-10(2)5-6-11-13(18-3)9-14-12(16(11)19-4)7-8-15(17)20-14/h5,7-9H,6H2,1-4H3
4335-12-0Relevant academic research and scientific papers
Efficient syntheses of 6-prenylcoumarins and linear pyranocoumarins: Total synthesis of suberosin, toddaculin, O-methylapigravin (O-methylbrosiperin), O-methylbalsamiferone, dihydroxanthyletin, xanthyletin and luvangetin
Mali, Raghao S.,Joshi, Priya P.,Sandhu, Paramjeet Kaur,Manekar-Tilve, Anita
, p. 371 - 376 (2007/10/03)
Synthesis of naturally occurring 6-prenylcoumarins (1a, 2c and 3a) and their derivatives 1c, 1d, 1e, 2d and 3b-d starting from 2-prenyloxybenzaldehydes (8, 12 and 14) using tandem Claisen rearrangement and Wittig reaction is described. The coumarins 1a, 1
Efficient Synthesis of 6-Prenylcoumarins; Total Syntheses of Suberosin, Toddaculin, O-Methylapigravin (O-Methylbrosiperin) and O-Methylbalsamiferone
Mali, Raghao S.,Sandhu, Paramjeet Kaur,Manekar-Tilve, Anita
, p. 251 - 252 (2007/10/02)
Synthesis of naturally occurring 6-prenylcoumarins 1a, b, 2c, and 3b and their derivatives 6a-c is described, starting from 2-prenyloxybenzaldehydes 4a-c, using a tandem Claisen rearrangement and Wittig reaction.
Synthesis of Toddanol and Toddanone
Sharma, Padam N.,Shoeb, Aboo,Kapil, Randhir S.,Popli, Satya P.
, p. 938 - 939 (2007/10/02)
A synthetic approach to confirm the structures of toddanol (1) and toddanone (2) has been provided.In addition, coumurrayin (12), sibiricin (13), isosiribicin (14), toddaculin (8) and aculeatin (9) have also been synthesised.
