65754-47-4 Usage
Uses
Given the provided materials, specific uses for Bicyclo[4.2.0]octa-1,3,5-triene-7-carbonyl chloride, 3-methoxy(9CI) are not explicitly detailed. However, based on the general properties of carbonyl chlorides, we can infer potential applications:
Used in Organic Synthesis:
Bicyclo[4.2.0]octa-1,3,5-triene-7-carbonyl chloride, 3-methoxy(9CI) is used as a reagent for introducing carbonyl groups into organic molecules, which is essential for the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its bicyclic structure and methoxy group may provide unique reactivity and selectivity in certain types of chemical reactions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Bicyclo[4.2.0]octa-1,3,5-triene-7-carbonyl chloride, 3-methoxy(9CI) could be utilized as an intermediate in the synthesis of complex organic molecules with potential medicinal properties. Its unique structural features may contribute to the development of novel drugs with specific therapeutic targets.
Used in Chemical Research:
Bicyclo[4.2.0]octa-1,3,5-triene-7-carbonyl chloride, 3-methoxy(9CI) may also serve as a subject of study in chemical research, where its reactivity, stability, and potential reactions with other compounds can be explored. This could lead to a better understanding of carbonyl chloride chemistry and the discovery of new synthetic pathways or applications.
Check Digit Verification of cas no
The CAS Registry Mumber 65754-47-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,7,5 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 65754-47:
(7*6)+(6*5)+(5*7)+(4*5)+(3*4)+(2*4)+(1*7)=154
154 % 10 = 4
So 65754-47-4 is a valid CAS Registry Number.
65754-47-4Relevant academic research and scientific papers
Wilmouth, Serge,Pellissier, Helene,Santelli, Maurice
, p. 10079 - 10088 (1998)
Titanium tetrachloride mediated dialkylation of acetic anhydride, trifluoroacetic anhydride or difluorochloroacetic anhydride by 1,8- bis(trimethylsilyl)-2,6-octadiene (BISTRO) leads, respectively, to dl- 1- methyl-2,5-divinylcyclopentan-1-ol dl-1-difluoromethyl-2,5- divinylcyclopentan-1-ol or dl-1-trifluoromethyl-2,5-divinylcyclopentan-1-ol. Esterification of these compounds with 4-methoxybenzocyclobutene-l-carboxylic acid and then pyrolysis led to 3-methoxy-12-oxa-17-vinylestra-1,3,5(10)- trien-11-one and to corresponding 18,18-difluoro or 18,18,18-trifluoro derivatives. Further transformations give rise to 3-methoxy- 12-oxa-17-(2- oxoethyl)- 18.18-difluoroestra-1,3,5(10)-trien-11-one and to the corresponding 18,18,18-trifluoro derivative.
