4337-95-5 Usage
Uses
Used in Organic Synthesis:
Tricyclo[2.2.1.0~2,6~]hept-3-ylmethanol is utilized as a synthetic building block in organic synthesis for its complex structure and potential reactivity. Its unique tricyclic framework allows for the creation of novel compounds with diverse applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, tricyclo[2.2.1.0~2,6~]hept-3-ylmethanol serves as a key intermediate in the synthesis of pharmaceutical compounds. Its tricyclic structure and reactivity contribute to the development of new drugs with potential therapeutic benefits.
Used in Chemical Reactivity Studies:
Tricyclo[2.2.1.0~2,6~]hept-3-ylmethanol is employed as a subject for studying ring strain and its impact on chemical reactivity. Understanding the effects of ring strain on tricyclo[2.2.1.0~2,6~]hept-3-ylmethanol can provide insights into the behavior of similar tricyclic structures and inform the design of new chemical reactions and processes.
Used in Research and Development:
This tricyclic compound is also used in research and development settings to explore its potential applications and properties. Its unique structure and reactivity make it an interesting target for further investigation, potentially leading to new discoveries and innovations in chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 4337-95-5 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 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4337-95:
(6*4)+(5*3)+(4*3)+(3*7)+(2*9)+(1*5)=95
95 % 10 = 5
So 4337-95-5 is a valid CAS Registry Number.
4337-95-5Relevant academic research and scientific papers
Experiments towards the Generation of 1,5- and 2,3-Didehydroquadricyclanes
Heywang, Ulrich,Szeimies, Guenter
, p. 121 - 131 (2007/10/02)
Metalation of the (hydroxymethyl)quadricyclanes 7a - c with n-butyllithium in ether is determined mostly by the chelating effect of the CH2O-Li group and only to a lesser extent by the magnitude of the 13C-1H coupling constant of the position to be lithiated in the corresponding quadricyclane derivative.Similar results were obtained for 3-quadricyclanol (20a).Treatment of the bromide 26a, prepared by lithiation of 7b, with strong bases apparently generates the 1,2-didehydroquadricyclane 34.and not the 1,5-didehydroquadricyclane 35.Attempts to convert the dihalide 9 into the 2,3-didehydroquadricyclane 4 were unsuccessful.
