36370-27-1 Usage
Uses
Used in Organic Synthesis:
1-[(benzyloxy)methyl]-2-oxocyclohexylmethyl 4-methylbenzenesulfonate is utilized as a key building block in organic synthesis, particularly for constructing complex molecular structures. Its unique combination of functional groups allows for further chemical modifications and the creation of novel compounds with tailored properties.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1-[(benzyloxy)methyl]-2-oxocyclohexylmethyl 4-methylbenzenesulfonate is used as a starting material or intermediate in the development of new drugs and bioactive compounds. The presence of the sulfonyl group and the cyclohexyl ring, both of which have been associated with biological activity, makes {1-[(benzyloxy)methyl]-2-oxocyclohexyl}methyl 4-methylbenzenesulfonate a promising candidate for the design and synthesis of potential therapeutic agents.
Overall, 1-[(benzyloxy)methyl]-2-oxocyclohexylmethyl 4-methylbenzenesulfonate is a versatile and valuable chemical compound with a wide range of potential applications in both organic synthesis and pharmaceutical research, thanks to its unique structural features and the possibility of creating complex molecules with diverse properties.
Check Digit Verification of cas no
The CAS Registry Mumber 36370-27-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,3,7 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 36370-27:
(7*3)+(6*6)+(5*3)+(4*7)+(3*0)+(2*2)+(1*7)=111
111 % 10 = 1
So 36370-27-1 is a valid CAS Registry Number.
36370-27-1Relevant academic research and scientific papers
One-Pot Oxapropellane Skeleton Formation Based on Conjugate Addition
Fang, Chenglin,Suganuma, Kyoko,Suemune, Hiroshi,Sakai, Kiyoshi
, p. 1549 - 1554 (2007/10/02)
Reactions of five- and/or six-membered-ring ketones 1-5 possessing an ω-halogenoalkyl group and α',β'-unsaturated ester function at the α-position with diorganocuprates afforded the oxapropellane compounds 20-24 in a one-pot, three-step procedure via 1,4-
