82214-69-5

Basic information

• Product Name: 2-BIPHENYLYLMAGNESIUM BROMIDE 0.5M IN
• Synonyms: 2-BIPHENYLYLMAGNESIUM BROMIDE 0.5M IN;2-BIPHENYLYLMAGNESIUM BROMIDE, 0.5M IN DIETHYL ETHER;2-biphenylmagnesium bromide solution;2-Biphenylmagnesium bromide solution 0.5 in diethyl ether;2-BiphenylMagnesiuM broMide, 0.5M solution in diethyl ether, J&KSeal;2-Biphenylmagnesium bromide solution 0.5 M in diethyl ether
• CAS NO: 82214-69-5
• Molecular Formula: C₁₂H₉BrMg
• Molecular Weight: 257.40886
• Product Categories: Aryl;Grignard Reagents;Organometallic Reagents
• Mol File: 82214-69-5.mol

Chemical Properties

• Flash Point: -40 °F
• Appearance: /
• Density: 0.800 g/mL at 25 °C(lit.)
• CAS DataBase Reference: 2-BIPHENYLYLMAGNESIUM BROMIDE 0.5M IN(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BIPHENYLYLMAGNESIUM BROMIDE 0.5M IN(82214-69-5)
• EPA Substance Registry System: 2-BIPHENYLYLMAGNESIUM BROMIDE 0.5M IN(82214-69-5)

Safety Data

• Hazard Codes: F+,C,F
• Statements: 12-19-22-34-67-14-11
• Safety Statements: 9-16-26-29-33-36/37/39-45
• RIDADR: UN 2924 3/PG 1
• WGK Germany: 1
• Hazardous Substances Data: 82214-69-5(Hazardous Substances Data)

Upstream product

• 2052-07-5 2-Bromobiphenyl 

Downstream Products

• 5660-38-8 [1,1';2',1'';3'',1''';4''',1'''']Quinquephenyl 
• 81483-62-7 hexakis-biphenyl-2-yl distannane 
• 127519-97-5 (o-C₆H₅C₆H₄)3SnBr 
• 100261-27-6 Biphenylyl-2-phenylborinsaeure-<2-amino-ethylester> 
• 84-15-1 o-terphenyl 
• 92-94-4 [1,1';4',1'']terphenyl 
• 92-52-4 biphenyl 
• 641-96-3 2,2'-diphenylbiphenyl 
• 6243-23-8 o-Quinquephenyl 
• 613-33-2 (4,4'-dimethyl-1,1'-biphenyl) 
• 42984-87-2 4-methyl-(1,1’,2’,1’’)terphenyl 
• 5660-37-7 2',2''-diphenyl-m-terphenyl 
• 14739-46-9 2,2''-diphenyl-p-terphenyl 
• 56692-39-8 2,2'''-diphenyl-m-quaterphenyl 

Relevant articles and documents

ORGANOMETALLIC COMPLEX, LIGHT-EMITTING ELEMENT, LIGHT-EMITTING DEVICE, ELECTRONIC DEVICE AND LIGHTING DEVICE

Provided is a novel substance that can emit phosphorescence. Alternatively, provided is a novel substance with high emission efficiency. An organometallic complex in which a 4-arylpyrimidine derivative is a ligand and iridium is a central metal is provided. Specifically, an organometallic complex having a structure represented by a general formula (G1) is provided. In the general formula (G1), R1 represents a substituted or unsubstituted alkyl group having 1 to 4 carbon atoms or a substituted or unsubstituted aryl group having 6 to 10 carbon atoms, R2 represents any of hydrogen, a substituted or unsubstituted alkyl group having 1 to 4 carbon atoms, and a substituted or unsubstituted phenyl group, R3 represents hydrogen or a substituted or unsubstituted alkyl group having 1 to 4 carbon atoms, and Ar1 represents a substituted or unsubstituted arylene group having 6 to 10 carbon atoms.

CHIRAL PHOSPHORUS COMPOUNDS

The present invention provides P-chiral compounds of general formula (II) and (III): wherein at least one of R21, R25, R26 and R30 is independently selected from C1-4 alkyl, CF3, C1-4 alkoxy, phenyl and benzyloxy and the remaining substituents selected from R21, R25, R26 and R30 are hydrogen; at least one of R22, R24, R27 and R29 are independently selected from C1-4 alkyl, CF3, C1-4 alkoxy, phenyl and benzyloxy and the remaining substituents selected from R22, R24, R27 and R29 are hydrogen; and R23 and R28 are independently selected from hydrogen, C1-4 alkyl, CF3, C1-4 alkoxy, phenyl and benzyloxy; Formula (III): wherein at least one of R21, R25, R26 and R30 is independently selected from phenyl and benzyloxy and the remaining substituents selected from R21, R25, R26 and R30 are hydrogen; and R22, R23, R24, R27, R28 and R29 are independently selected from hydrogen, C1-4 alkyl, CF3, C1-4 alkoxy, phenyl and benzyloxy.wherein at least one of R21, R25, R26 and R30 is independently selected from phenyl and benzyloxy and the remaining substituents selected from R21, R25, R26 and R30 are hydrogen; and R22, R23, R24, R27, R28 and R29 are independently selected from hydrogen, C1-4 alkyl, CF3, C1-4 alkoxy, phenyl and benzyloxy.

SPIROFLUORENE DERIVATIVE, MATERIAL FOR LIGHT-EMITTING ELEMENT, LIGHT-EMITTING ELEMENT, LIGHT-EMITTING DEVICE, AND ELECTRONIC DEVICE

It is an object of the present invention to provide a material having a high Tg and a wide energy gap. The present invention provides a spirofluorene derivative represented by General Formula 1. (In the formula, R1 is any one of hydrogen, an alkyl group having 1 to 4 carbon atoms, or a group represented by General Formula 2. Each of R2 and R3 is either hydrogen or an alkyl group having 1 to 4 carbon atoms and may be identical or different. R4 is an aryl group having 6 to 15 carbon atoms. Each of R5 and R6 is any one of hydrogen, an alkyl group having 1 to 4 carbon atoms, or an aryl group having 6 to 15 carbon atoms and may be identical or different.)

ANTHRACENE DERIVATIVES AND ORGANIC ELECTROLUMINESCENT DEVICES MADE BY USING THE SAME

An anthracene derivative represented by the following general formula (1) which enables an organic electroluminescence device to exhibit a great efficiency of light emission and uniform light emission even at high temperatures since crystallization is suppressed and no thermal decomposition takes place during vapor deposition and an organic electroluminescence device utilizing the derivative, are provided. [Ar represents a group represented by the following general formula (2): (L1 and L2 each represent a substituted or unsubstituted methylene group, ethylene group or the like, and at least one of them is present), Ar' represents a substituted or unsubstituted aryl group having 6 to 50 nuclear carbon atoms, X represent an alkyl group or the like, a and b each represent an integer of 0 to 4, and n represents an integer of 1 to 3.]