334700-48-0 Usage
Uses
Used in Pharmaceutical Industry:
(2S,3S,4aR,8aR)-2,3,4a,8a-Tetrahydro-7-iodo-2,3-diMethoxy-2,3-diMethyl-1,4-benzodioxin-6(5H)-one is used as an intermediate in the synthesis of (-)-Altenuene (A575740), a toxin isolated from the fungus Alternaria tenuis. (2S,3S,4aR,8aR)-2,3,4a,8a-Tetrahydro-7-iodo-2,3-diMethoxy-2,3-diMethyl-1,4-benzodioxin-6(5H)-one has potential applications in the development of new drugs and therapies, particularly in the field of pharmacology.
Additionally, due to its structural complexity and unique features, (2S,3S,4aR,8aR)-2,3,4a,8a-Tetrahydro-7-iodo-2,3-diMethoxy-2,3-diMethyl-1,4-benzodioxin-6(5H)-one may also be used as a starting material or building block in the synthesis of other complex organic molecules with potential applications in various industries, such as agrochemicals, materials science, and chemical research.
Check Digit Verification of cas no
The CAS Registry Mumber 334700-48-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,4,7,0 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 334700-48:
(8*3)+(7*3)+(6*4)+(5*7)+(4*0)+(3*0)+(2*4)+(1*8)=120
120 % 10 = 0
So 334700-48-0 is a valid CAS Registry Number.
334700-48-0Relevant academic research and scientific papers
Approaches to the synthesis of (+)- and (-)-epibatidine
Barros, M. Teresa,Maycock, Christopher D.,Ventura, M. Rita
, p. 166 - 173 (2007/10/03)
Synthetic approaches to the powerful analgesic alkaloids (+)- and (-)-epibatidine are described. The starting material employed was natural (-)-quinic acid from which chiral enones and α-iodoenones were prepared. Stille coupling afforded suitable substrat
