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LITHIUM TETRA(PERFLUORO-T-BUTOXY)ALUMINATE is a compound that is widely recognized for its role as a mild Lewis acid catalyst in organic syntheses. It is a versatile reagent with a notable capacity to activate a range of substrates, especially in fluorine chemistry. LITHIUM TETRA(PERFLUORO-T-BUTOXY)ALUMINATE is characterized by its stability and reactivity, making it a valuable asset in the field of chemical research and industry.

274933-96-9

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274933-96-9 Usage

Uses

Used in Organic Synthesis:
LITHIUM TETRA(PERFLUORO-T-BUTOXY)ALUMINATE is used as a catalyst for facilitating various organic reactions, enhancing the efficiency and selectivity of the synthesis processes. Its mild Lewis acidity allows for controlled activation of substrates without causing unwanted side reactions.
Used in Fluorine Chemistry:
In the realm of fluorine chemistry, LITHIUM TETRA(PERFLUORO-T-BUTOXY)ALUMINATE is used as a reagent to activate fluorinated compounds, enabling the formation of new carbon-fluorine bonds and the synthesis of complex fluorinated molecules.
Used in Pharmaceutical Development:
LITHIUM TETRA(PERFLUORO-T-BUTOXY)ALUMINATE is employed in the preparation of fluorinated organic compounds that are integral to the development of new pharmaceuticals. Its ability to stabilize and activate fluorinated substrates is crucial for the synthesis of potential drug candidates.
Used in Materials Science:
In the field of materials science, LITHIUM TETRA(PERFLUORO-T-BUTOXY)ALUMINATE is used as a component in the development of new materials, particularly those that require fluorinated components for enhanced properties such as chemical stability or electronic characteristics.
Used in Energy Storage:
LITHIUM TETRA(PERFLUORO-T-BUTOXY)ALUMINATE is used in lithium-ion battery research as a means to stabilize electrolytes and improve overall battery performance. Its application in this industry is significant for advancing energy storage technologies and contributing to the development of more efficient and sustainable power sources.

Check Digit Verification of cas no

The CAS Registry Mumber 274933-96-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,4,9,3 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 274933-96:
(8*2)+(7*7)+(6*4)+(5*9)+(4*3)+(3*3)+(2*9)+(1*6)=179
179 % 10 = 9
So 274933-96-9 is a valid CAS Registry Number.

274933-96-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Lithium tetra(perfluoro-t-butoxy)aluminate, min. 98%

1.2 Other means of identification

Product number -
Other names -

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

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

More Details:274933-96-9 SDS

274933-96-9Relevant academic research and scientific papers

ELECTROLYTE SALTS FOR RECHARGEABLE MAGNESIUM-ION BATTERIES

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Paragraph 0054, (2020/03/28)

Magnesium salts suitable for use in an electrolyte for a magnesium ion electrochemical cell are described herein. The salts are magnesium tetra(perfluoroalkoxy)metalates, optionally solvated with up to seven ether molecules coordinated to the magnesium ion thereof. In one embodiment, the salt has the empirical formula: Mg(Z)22+[M(OCR3)4?]2 (Formula (I)) wherein Z is an ether; n is 0 to about 7; M is Al or B; and each R independently is a perfluoroalkyl group (e.g., C1 to C10 perfluoroalkyl). The magnesium salts of Formula (I) are suitable for use as electrolyte salts for magnesium ion batteries (e.g., 5 V class magnesium batteries) and exhibit a wide redox window that is particularly compatible with magnesium anode. The salts are relatively cost effective to prepare by methods described herein, which are conveniently scalable to levels suitable for commercial production.

Preparation method and application of silver auxiliary

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Paragraph 0039-0040, (2017/06/02)

The invention relates to a method for preparing a silver auxiliary AgAl(ORF)4. The method comprises the following steps that 1, HORF reacts with LiAlH4 to generate a lithium-aluminum compound LiAl(ORF)4; 2, the lithium-aluminum compound LiAl(ORF)4 obtained in the step 1 reacts with AgBF4 to generate a compound AgAl(ORF)4, wherein RF is a C1-C5 hydrocarbyl group, and hydrogen atoms on the hydrocarbyl group are optionally replaced with fluorine atoms. The invention further relates to application of the silver auxiliary in an ethylene tetramerization technology. The preparation method is simple, 1-octene can be highly selectively produced when the silver auxiliary is applied in ethylene tetramerization, and the selectivity of 1-octene is higher than 60%.

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