73244-35-6 Usage
Molecular structure
1-(5-bromopent-2-en-2-yl)-4-methoxybenzene consists of a benzene ring connected to a 5-bromopent-2-en-2-yl group and a 4-methoxy group.
Class of compound
Aromatic compounds.
Functional groups
Contains both alkene and halogen functional groups.
Usage
Utilized in organic synthesis and chemical research as a building block for creating more complex molecules.
Chemical properties
The presence of bromine and methoxy groups gives 1-(5-bromopent-2-en-2-yl)-4-methoxybenzene specific chemical properties.
Industrial and scientific applications
Useful for various industrial and scientific applications due to its unique chemical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 73244-35-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,2,4 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 73244-35:
(7*7)+(6*3)+(5*2)+(4*4)+(3*4)+(2*3)+(1*5)=116
116 % 10 = 6
So 73244-35-6 is a valid CAS Registry Number.
73244-35-6Relevant academic research and scientific papers
Enantioselective Bromolactonization of Trisubstituted Olefinic Acids Catalyzed by Chiral Pyridyl Phosphoramides
Nishikawa, Yasuhiro,Hamamoto, Yuhta,Satoh, Rika,Akada, Naho,Kajita, Shuhei,Nomoto, Marina,Miyata, Megumi,Nakamura, Madoka,Matsubara, Chinatsu,Hara, Osamu
supporting information, p. 18880 - 18885 (2018/12/04)
Enantioselective bromolactonization of trisubstituted olefinic acids producing synthetically useful chiral lactones with two contiguous asymmetric centers has remained mainly unexplored except for the 6-exo cyclization mode. In this work, the 5-exo- and 6
