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

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

Uses

Used in Organic Synthesis:
3 7-DIMETHYLOCTYLMAGNESIUM BROMIDE 1.0& is used as a reagent for the formation of carbon-carbon bonds, which is essential in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3 7-DIMETHYLOCTYLMAGNESIUM BROMIDE 1.0& is used as a catalyst or a source of magnesium in Grignard reactions, facilitating the production of various pharmaceutical compounds.
Used in Agrochemical Industry:
3 7-DIMETHYLOCTYLMAGNESIUM BROMIDE 1.0& is utilized in the synthesis of agrochemicals, contributing to the development of pesticides and other agricultural chemicals that are vital for crop protection and yield enhancement.
Used in Fine Chemicals Production:
3 7-DIMETHYLOCTYLMAGNESIUM BROMIDE 1.0& is also used in the production of fine chemicals, where its reactivity and selectivity are harnessed to create specialty chemicals for various applications, including fragrances, dyes, and other high-value products.

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 
• 74514-19-5 (2E)-6-chloro-3,7-dimethyl-2,7-octadienyl acetate 
• 106-21-8 tetrahydrogeraniol 

Downstream Products

• 347390-12-9 4,4'-bis(3,7-dimethyloctanyl)diphenylacetylene 
• 381211-07-0 1-(3,7-dimethyloctananyl)-4-iodobenzene 
• 1357584-03-2 3,3''-(3',7'-dimethyloctyl)-2,2':5,2''-terthiophene 
• 1406-70-8 (2R,4'RS,8'RS)-α-tocopheryl acetate 
• 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 

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.

Process for the preparation of terpenes

A terpene compound having the formula (III) is produced by reacting an allylic halide having the formula (I) with a Grignard reagent having the formula (II) in the presence of anhydrous zinc chloride and a copper compound or an organic zinc halide compound having the formula (IV) in the presence of a copper compound, provided that when A-A is C-C, R' is hydrogen and when A-A is C=C, X is chlorine. STR1