911836-38-9 Usage
General Description
1-bromo-5-phenylnaphthalene is a chemical compound with the molecular formula C16H11Br. It is a brominated naphthalene derivative with a phenyl group attached to the 5th carbon atom. 1-bromo-5-phenylnaphthalene is used in various organic synthesis reactions and is also being studied for its potential use in electronic materials and as a fluorescent material. 1-bromo-5-phenylnaphthalene is known for its ability to undergo substitution reactions and for its potential use in the development of organic electronic devices. It is important to handle this compound with caution, as it is considered hazardous if ingested, inhaled, or absorbed through the skin. Safety precautions should be followed when working with 1-bromo-5-phenylnaphthalene, including the use of appropriate personal protective equipment and working in a well-ventilated area.
Check Digit Verification of cas no
The CAS Registry Mumber 911836-38-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,1,8,3 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 911836-38:
(8*9)+(7*1)+(6*1)+(5*8)+(4*3)+(3*6)+(2*3)+(1*8)=169
169 % 10 = 9
So 911836-38-9 is a valid CAS Registry Number.
911836-38-9Relevant articles and documents
ORGANIC ELECTROLUMINESCENT ELEMENT AND MONOAMINE COMPOUND FOR ORGANIC ELECTROLUMINESCENT ELEMENT
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Paragraph 0123; 0124; 0125; 0126, (2019/09/05)
PROBLEM TO BE SOLVED: To provide an organic electroluminescent element with high efficiency and an amine compound therefor. SOLUTION: The amine compound for organic electroluminescent element is a monoamine compound expressed by the compound, the compound
Diastereoselective synthesis of β-aryl-C-nucleosides from 1,2-anhydrosugars
Singh, Ishwar,Seitz, Oliver
, p. 4319 - 4322 (2007/10/03)
(Chemical Equation Presented) The cis opening of glycal epoxides with arylaluminum reagents provides strict stereocontrol in C-glycosylation. β-Aryl-C-2-deoxynucleosides are obtained from known glycals by an epoxidation-glycosylation-deoxygenation sequenc