64689-70-9 Usage
Uses
Used in Organic Synthesis:
1-Bromo-2-Methoxymethylnaphthalene is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows it to participate in a range of chemical reactions, making it a valuable component in the development of new molecules and materials.
Used in Pharmaceutical Industry:
1-Bromo-2-Methoxymethylnaphthalene is used as a building block in the design and synthesis of pharmaceutical compounds. Its potential reactivity and structural features make it a promising candidate for the creation of new drugs and therapeutic agents.
Used in Material Science:
1-Bromo-2-Methoxymethylnaphthalene is used as a component in the development of advanced materials with specific properties. Its incorporation into material systems can lead to the creation of novel materials with improved characteristics, such as enhanced stability, reactivity, or other desirable traits.
Used in Research and Development:
1-Bromo-2-Methoxymethylnaphthalene is used as a research tool in the exploration of new chemical reactions and processes. Its unique properties and potential reactivity make it an interesting subject for study, contributing to the advancement of scientific knowledge and the development of new technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 64689-70-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,6,8 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 64689-70:
(7*6)+(6*4)+(5*6)+(4*8)+(3*9)+(2*7)+(1*0)=169
169 % 10 = 9
So 64689-70-9 is a valid CAS Registry Number.
64689-70-9Relevant academic research and scientific papers
Synthesis of Naphthocyclobutenes from α-Naphthyl Acrylates by Visible-Light Energy-Transfer Catalysis
Peez, Theodor,Schmalz, Veronika,Harms, Klaus,Koert, Ulrich
, p. 4365 - 4369 (2019/06/14)
Methyl (α-naphthyl) acrylates bearing an ortho-substituent with a hydrogen atom produce naphthocyclobutenes upon Ir(Fppy)3-mediated photosensitization. This reaction can be described as a carbon analogue of the Norrish-Yang reaction: upon triplet excitation of the acrylate a 1,5-HAT results in a 1,4-diradical which forms the cyclobutene. Diastereoselectivities up to >20:1 were observed for the ring-closure reaction.
