61982-86-3 Usage
Naphthalene family
1-Methoxy-5-phenylnaphthalene belongs to the naphthalene family, which is a group of organic compounds consisting of two fused benzene rings.
Industrial applications
1-Methoxy-5-phenylnaphthalene is widely used in the pharmaceutical and chemical industries as a building block for synthesizing various organic compounds.
Fluorescence properties
The compound exhibits strong fluorescence, making it useful in the development of fluorescent dyes and markers.
Optoelectronic applications
1-Methoxy-5-phenylnaphthalene has been studied for its potential use in organic light-emitting diodes (OLEDs) and other optoelectronic applications due to its unique optical and electronic properties.
Health and environmental hazards
It is important to handle 1-Methoxy-5-phenylnaphthalene with care, as it may pose health and environmental risks if not used and disposed of properly.
Check Digit Verification of cas no
The CAS Registry Mumber 61982-86-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,9,8 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 61982-86:
(7*6)+(6*1)+(5*9)+(4*8)+(3*2)+(2*8)+(1*6)=153
153 % 10 = 3
So 61982-86-3 is a valid CAS Registry Number.
61982-86-3Relevant articles and documents
Synthesis of naphthalene derivatives through inexpensive BF 3·Et2O-catalyzed annulation reaction of arylacetaldehydes with arylalkynes
Xiang, Shikai,Hu, Hao,Ma, Jing,Li, Yuanzhuo,Wang, Biqin,Feng, Chun,Zhao, Keqing,Hu, Ping,Chen, Xiaozhen
, p. 945 - 951 (2013/08/23)
An inexpensive BF3·Et2O-catalyzed annulation reaction of arylacetaldehydes with arylalkynes has been developed. Various substituted phenylacetaldehydes and phenylacetylenes can undergo this reaction, producing corresponding α-aryl su
A single-step procedure for the preparation of palladium nanoparticles and a phosphine-functionalized support as catalyst for Suzuki cross-coupling reactions
Costa, Natalia J.S.,Kiyohara, Pedro K.,Monteiro, Adriano L.,Coppel, Yannick,Philippot, Karine,Rossi, Liane M.
experimental part, p. 382 - 389 (2011/02/27)
We here report the preparation of supported palladium nanoparticles (NPs) stabilized by pendant phosphine groups by reacting a palladium complex containing the ligand 2-(diphenylphosphino)benzaldehyde with an amino-functionalized silica surface. The Pd na
