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Triisopropylgallium, with the chemical formula C9H21Ga, is an organogallium compound that features a gallium atom bonded to three isopropyl groups. It is a colorless, volatile, and moisture-sensitive liquid, which is soluble in organic solvents. Triisopropylgallium is primarily used as a reagent in organic synthesis, particularly in the formation of carbon-carbon bonds and as a catalyst in various chemical reactions. Due to its reactivity with water and oxygen, it must be handled under an inert atmosphere. Triisopropylgallium is also known for its potential applications in the synthesis of gallium-containing materials for electronic and optoelectronic devices.

54514-59-9

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54514-59-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54514-59-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,5,1 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 54514-59:
(7*5)+(6*4)+(5*5)+(4*1)+(3*4)+(2*5)+(1*9)=119
119 % 10 = 9
So 54514-59-9 is a valid CAS Registry Number.

54514-59-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name tri(propan-2-yl)gallane

1.2 Other means of identification

Product number -
Other names Gallium,tris(1-methylethyl)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:54514-59-9 SDS

54514-59-9Downstream Products

54514-59-9Relevant academic research and scientific papers

Metalated diphosphanylsiloxanes with polycyclic and polymeric structures

von H?nisch, Carsten,Stahl, Sven

, p. 2780 - 2783 (2007)

The reactions of the diphosphanylsiloxane O(SiiPr2PH2)2 (1) with MiPr3 (M = Ga, In) produced the polycyclic compounds [O{SiiPr2(PH)MiPr2}{SiiPr2(P)MiPr}] 2 (2, 3). Compounds 2 and 3 are composed of three M2P2 rings forming a ladder structure and two OSi2P2M rings. By reactions of 1 with n-BuLi the polymeric compound [O(SiiPr2PHLi)2(THF)(TMEDA)] · THF (4) was obtained.

The reactions of dialkylgallium hydrides with tert-butylethynylbenzenes - A systematic investigation into the course of hydrogallation reactions

Uhl, Werner,Claesener, Michael,Haddadpour, Sima,Jasper, Beate,Hepp, Alexander

, p. 417 - 423 (2008/01/27)

The reactions of bis- and tris(tert-butylethynyl)benzenes with dialkylgallium hydrides afforded two different types of products. 1,4-Di(tert-butylethynyl)benzene and dialkylgallium hydrides R2GaH bearing relatively small substituents (R = Et, nPr) gave the expected addition products with each CC triple bond inserted into a Ga-H bond. The intact GaR 2 groups are attached to those carbon atoms which are in α-position to the benzene rings, and intermolecular Ga-C interactions led to the formation of one-dimensional coordination polymers. In contrast secondary reactions with the release of the corresponding trialkylgallium derivatives GaR3 (R = Et, nPr, iPr, CH2tBu, tBu) were observed for all hydrogallation reactions involving the trisalkyne 1,3,5-tris(tert-butylethynyl) benzene. A similar reaction was observed upon treatment of the 1,4-bisalkyne with a dialkylgallium hydride bearing a relatively bulky substituent (R = neopentyl). Cyclophane type molecules are formed in all these cases with two or three gallium atoms in the bridging positions between both benzene rings. The Royal Society of Chemistry.

Preparation of organometal compounds

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Page 6, (2008/06/13)

A method of preparing organometal compounds that does not use oxygenated solvents is provided. The compounds produced by such method are particularly useful as precursor compounds for metalorganic chemical vapor deposition processes used in the manufacture of electronic devices. Methods of depositing metal films using such organometal compounds are also provided.

Metalorganic compounds

-

, (2008/06/13)

A process is provided for the production of metalorganic compounds by reacting a Grignard reagent with a Group II, Group III or Group V metal halide in a tertiary alkyl amine solvent to form a metalorganic adduct, isolating the adduct and dissociating the adduct to leave the metalorganic compound.

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