34969-65-8 Usage
Uses
Used in Pharmaceutical Industry:
(1R,2R)-1,2-dibromocyclooctane is utilized as an intermediate in the synthesis of various organic compounds, particularly in the pharmaceutical industry. Its molecular structure and stereochemistry are instrumental in creating complex molecules with specific chirality, which is crucial for the development of new drugs with targeted therapeutic effects.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, (1R,2R)-1,2-dibromocyclooctane serves as an intermediate for the synthesis of organic compounds. Its unique properties allow for the development of agrochemicals with precise actions, potentially leading to more effective and targeted pest control solutions.
Used in Scientific Research:
(1R,2R)-1,2-dibromocyclooctane is also employed in scientific research, where its properties can be explored and harnessed for various experimental purposes. Researchers can use (1R,2R)-1,2-dibromocyclooctane to study chemical reactions, mechanisms, and the development of new synthetic methodologies.
Used as a Reagent in Organic Synthesis Reactions:
In addition to its role as an intermediate, (1R,2R)-1,2-dibromocyclooctane is used as a reagent in organic synthesis reactions. Its reactivity and selectivity can be leveraged to facilitate specific chemical transformations, contributing to the synthesis of desired products with high yields and purity.
It is important to handle (1R,2R)-1,2-dibromocyclooctane with care due to its toxic and potentially hazardous nature. Proper safety measures should be taken to minimize risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 34969-65-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,9,6 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 34969-65:
(7*3)+(6*4)+(5*9)+(4*6)+(3*9)+(2*6)+(1*5)=158
158 % 10 = 8
So 34969-65-8 is a valid CAS Registry Number.
34969-65-8Relevant academic research and scientific papers
Revisiting the bromination of c-h bonds with molecular bromine by using a photo-microflow system
Manabe, Yoshiyuki,Kitawaki, Yuriko,Nagasaki, Masahiro,Fukase, Koichi,Matsubara, Hiroshi,Hino, Yoshiko,Fukuyama, Takahide,Ryu, Ilhyong
supporting information, p. 12750 - 12753 (2015/03/30)
The photobromination of C-H bonds by using molecular bromine was reinvestigated under microfluidic conditions. The continuous-flow method suppressed the production of dibrominated compounds and effectively produced the desired monobrominated products with high selectivity. Rapid bromination of benzylic substrates containing a photoaffinity azide group was achieved without any decomposition. Go with the (micro)flow: Photobromination of C-H bonds by using molecular bromine under microfluidic conditions has been investigated (see scheme). The continuous-flow method suppressed the production of dibrominated compounds and effectively produced the desired monobrominated compounds with high selectivity. Rapid bromination of benzylic substrates containing a photoaffinity azide group was achieved without any decomposition.
