114499-45-5

Basic information

• Product Name: 3 7-DIMETHYLOCTYLMAGNESIUM BROMIDE 1.0&
• Synonyms: 3 7-DIMETHYLOCTYLMAGNESIUM BROMIDE 1.0&;3,7-dimethyloctylmagnesium bromide solution;3,7-Dimethyloctylmagnesium bromide solution 1.0 in diethyl ether;3,7-DiMethyloctylMagnesiuM broMide solution 1.0 M in diethyl ether
• CAS NO: 114499-45-5
• Molecular Formula: C₁₀H₂₁BrMg
• Molecular Weight: 245.48
• Product Categories: Alkyl;Grignard Reagents;Organometallic Reagents
• Mol File: 114499-45-5.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 159.7 °C at 760 mmHg
• Flash Point: -13 °F
• Appearance: /
• Density: 0.856 g/mL at 25 °C
• Vapor Pressure: 3.21mmHg at 25°C
• CAS DataBase Reference: 3 7-DIMETHYLOCTYLMAGNESIUM BROMIDE 1.0&(CAS DataBase Reference)
• NIST Chemistry Reference: 3 7-DIMETHYLOCTYLMAGNESIUM BROMIDE 1.0&(114499-45-5)
• EPA Substance Registry System: 3 7-DIMETHYLOCTYLMAGNESIUM BROMIDE 1.0&(114499-45-5)

Safety Data

• Hazard Codes: F+,Xn,C
• Statements: 12-19-22-66-67-34-14
• Safety Statements: 9-16-29-33-45-36/37/39-26
• RIDADR: UN 1155 3/PG 1
• WGK Germany: 1
• Hazardous Substances Data: 114499-45-5(Hazardous Substances Data)

Usage

General Description

3 7-DIMETHYLOCTYLMAGNESIUM BROMIDE 1.0 is a chemical compound that consists of a magnesium atom bonded to an octyl group and two methyl groups, with a bromide ion attached. It is commonly used as a reagent in organic synthesis, particularly in the formation of carbon-carbon bonds. 3 7-DIMETHYLOCTYLMAGNESIUM BROMIDE 1.0& is known for its high reactivity and selectivity in various organic reactions, making it a valuable tool for chemists in the development of new molecules and compounds. It is often used as a catalyst or a source of magnesium in Grignard reactions, which are important processes in the production of pharmaceuticals, agrochemicals, and fine chemicals.

InChI:InChI=1/C10H21.BrH.Mg/c1-5-10(4)8-6-7-9(2)3;;/h9-10H,1,5-8H2,2-4H3;1H;/q-1;;+2/p-1

Upstream product

• 133953-62-5 3,7-dimethyloctylzinc chloride 
• 59965-20-7 1-bromo-3,7-dimethyloctane 
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• 106-21-8 tetrahydrogeraniol 

Downstream Products

• 381211-07-0 1-(3,7-dimethyloctananyl)-4-iodobenzene 
• 1357584-03-2 3,3''-(3',7'-dimethyloctyl)-2,2':5,2''-terthiophene 
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• 895518-38-4 vitamin E 
• 347390-26-5 2,3,4,5-tetrakis(4-(3,7-dimethyloctanyl)phenyl)cyclopentadienone 
• 347390-24-3 4,4'-(3,7-dimethyloctanyl)benzil 
• 347390-33-4 4-bromo-4'-(3,7-dimethyloctanyl)-diphenylacetylene 
• 347390-30-1 4-(3',7'-dimethyloctanyl)phenylacetylene 
• 347390-20-9 1,3-bis(4-(3,7-dimethyloctanyl)phenyl)-2-propanone ethylene acetal 
• 347390-28-7 4-(3,7-dimethyloctanyl)-trimethylsilylethinylbenzene 
• 347390-12-9 4,4'-bis(3,7-dimethyloctanyl)diphenylacetylene 

Relevant articles and documents

NEAR-INFRARED ABSORPTION COMPOSITION, CURED FILM, NEAR-INFRARED CUT FILTER, SOLID-STATE IMAGING DEVICE, INFRARED SENSOR, AND COMPOUND

To provide a near-infrared absorption composition which contains a squarylium compound having excellent solvent solubility, a cured film which uses the near-infrared absorption composition, a near-infrared cut filter, a solid-state imaging device, an infrared sensor, and a compound. A near-infrared absorption composition includes a compound represented by the following Formula (1) and a resin. R1 and R2 each independently represent “—S1-L1-T1” or the like, R3 and R4 each independently represent a hydrogen atom or an alkyl group, X1 and X2 each independently represent an oxygen atom or —N(R5)—, R5 represents a hydrogen atom or the like, Y1 to Y4 each independently represent a substituent, p and s each independently represent an integer of 0 to 3, and q and r each independently represent an integer of 0 to 2; and S1 represents an arylene group or the like, L1 represents an alkylene group or the like, and T1 represents an alkyl group or the like.