121609-44-7 Usage
Uses
Used in Pharmaceutical Synthesis:
(3-Methylcyclobutyl)acetic acid is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows it to be incorporated into complex organic molecules, contributing to the development of new and effective medications.
Used in Organic Compounds Synthesis:
In the field of organic chemistry, (3-Methylcyclobutyl)acetic acid serves as a building block for the creation of a wide range of organic compounds. Its versatility in forming carbon-carbon bonds and introducing new functional groups makes it an essential component in organic synthesis.
Used in Organic Chemistry Laboratories:
(3-Methylcyclobutyl)acetic acid is utilized as a reagent in organic chemistry laboratories for various purposes. It plays a crucial role in the formation of carbon-carbon bonds and the creation of new functional groups, which are essential for advancing research and development in organic chemistry.
Overall, (3-Methylcyclobutyl)acetic acid is a vital chemical compound that finds applications across different industries, particularly in pharmaceutical synthesis and organic chemistry research. Its unique structural properties and versatility in forming bonds and functional groups make it an indispensable component in the development of new and innovative products.
Check Digit Verification of cas no
The CAS Registry Mumber 121609-44-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,6,0 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 121609-44:
(8*1)+(7*2)+(6*1)+(5*6)+(4*0)+(3*9)+(2*4)+(1*4)=97
97 % 10 = 7
So 121609-44-7 is a valid CAS Registry Number.
121609-44-7Relevant articles and documents
Synthesis and Liquid Crystal Properties of Dimethylene Linked Compounds Incorporating the Cyclobutane or Spiroheptane Rings
Chan, L. K. M.,Gemmell, P. A.,Gray, G. W.,Lacey, D.,Toyne, K. J.
, p. 229 - 246 (2007/10/02)
The preparation of sixteen dimethylene linked compounds is described heptane ring>, and a comparison is made between the transition temperatures of these compounds and those of the corresponding esters.This comparison once again highlights the fact that the cyclobutane ring should be regarded, in terms of its ability to promote nematic thermal stability, as a "chain stiffener rather than as a ring system.A comparison is also made of the nematic thermal stabilities of the trans-cyclobutane and the spiroheptane systems and of the trans-cyclohexane and the spiroundecane systems.
