2530-99-6 Usage
Description
1-Allyl-3,7-dimethylxanthine is a chemical compound belonging to the xanthine class, with the molecular formula C11H14N4O2. It is closely related to caffeine and theobromine and exhibits a range of pharmacological effects, including central nervous system stimulation, vasodilation, and potential anti-inflammatory and anti-cancer properties.
Uses
Used in Pharmaceutical Industry:
1-Allyl-3,7-dimethylxanthine is used as a central nervous system stimulant for increasing alertness and improving cognitive function, similar to the effects of caffeine.
Used in Cardiovascular Applications:
As a vasodilator, 1-Allyl-3,7-dimethylxanthine is used in the treatment of cardiovascular disorders to improve blood flow and reduce strain on the heart.
Used in Respiratory Treatment:
1-Allyl-3,7-dimethylxanthine is used in the treatment of respiratory diseases, potentially aiding in the management of conditions such as asthma or chronic obstructive pulmonary disease (COPD) by relaxing the airways and improving breathing.
Used in Anti-inflammatory Applications:
Due to its potential anti-inflammatory properties, 1-Allyl-3,7-dimethylxanthine may be used in the development of treatments for inflammatory conditions, helping to reduce inflammation and alleviate symptoms.
Used in Oncology Research:
1-Allyl-3,7-dimethylxanthine is studied for its potential anti-cancer properties, with ongoing research exploring its use in the development of cancer therapies and its effects on various types of cancer cells.
Check Digit Verification of cas no
The CAS Registry Mumber 2530-99-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,3 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2530-99:
(6*2)+(5*5)+(4*3)+(3*0)+(2*9)+(1*9)=76
76 % 10 = 6
So 2530-99-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H12N4O2/c1-4-5-14-9(15)7-8(11-6-12(7)2)13(3)10(14)16/h4,6H,1,5H2,2-3H3
2530-99-6Relevant articles and documents
Reaction of 1-Allyl(methallyl)theobromine with Halogens
Petrova, K. Yu.,Kim,Eltsov,Eremenko
, p. 697 - 700 (2019)
The reactions of bromine and iodine with 1-allyltheobromine and 1-methallyltheobromine were studied. Depending on the nature of the halogen and the initial theobromine, the reaction can lead to the formation of the adducts at the double bond, oxazolopurines or complex compounds.
Synthesis of PS-supported NHC-Pd catalyst derived from theobromine and its applications in Suzuki-Miyaura reaction
Lo, Hung-Kun,Luo, Fen-Tair
experimental part, p. 394 - 398 (2012/08/08)
The synthesis of the PS-supported bis-NHC-palladium catalyst simply prepared from theobromine in four steps was reported. The air-stable PS-supported bis-NHC-Pd catalyst can be used as a good catalyst in running Suzuki-Miyaura cross-coupling reaction.
Highly efficient C-8 oxidation of substituted xanthines with substitution at the 1-, 3-, and 7- Positions using biocatalysts
Madyastha,Sridhar
, p. 677 - 680 (2007/10/03)
A bacterial consortium consisting of strains belonging to the genus Klebsiella and Rhodococcus quantitatively converts 1-, 3- and 7-substituted xanthines to their respective 8-oxo compounds.
