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87736-75-2

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87736-75-2 Usage

Description

1-[4-[[[(1,1-DiMethylethyl)diMethylsilyl]oxy]Methyl]phenyl]-2,2,2-trifluoro-ethanone is a light yellow oil with unique chemical properties. It is an intermediate compound that plays a significant role in the synthesis of trifluoromethyldiazirine, a valuable molecule for scientific research and applications.

Uses

Used in Chemical Research:
1-[4-[[[(1,1-DiMethylethyl)diMethylsilyl]oxy]Methyl]phenyl]-2,2,2-trifluoro-ethanone is used as an intermediate in the preparation of trifluoromethyldiazirine for chemical research purposes. Trifluoromethyldiazirine is a photo-induced cross-linking probe that aids in exploring amyloid formation, a crucial area of study in understanding various diseases and developing potential treatments.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-[4-[[[(1,1-DiMethylethyl)diMethylsilyl]oxy]Methyl]phenyl]-2,2,2-trifluoro-ethanone serves as a key intermediate in the synthesis of trifluoromethyldiazirine. 1-[4-[[[(1,1-DiMethylethyl)diMethylsilyl]oxy]Methyl]phenyl]-2,2,2-trifluoro-ethanone is utilized in the development of drugs targeting amyloid-related diseases, such as Alzheimer's and Parkinson's, by enabling researchers to study the formation and structure of amyloid proteins.
Used in Material Science:
1-[4-[[[(1,1-DiMethylethyl)diMethylsilyl]oxy]Methyl]phenyl]-2,2,2-trifluoro-ethanone is also used in material science as an intermediate for the synthesis of trifluoromethyldiazirine. 1-[4-[[[(1,1-DiMethylethyl)diMethylsilyl]oxy]Methyl]phenyl]-2,2,2-trifluoro-ethanone has potential applications in the development of advanced materials with unique properties, such as improved stability and reactivity, which can be beneficial in various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 87736-75-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,7,3 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 87736-75:
(7*8)+(6*7)+(5*7)+(4*3)+(3*6)+(2*7)+(1*5)=182
182 % 10 = 2
So 87736-75-2 is a valid CAS Registry Number.

87736-75-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[4-[[tert-butyl(dimethyl)silyl]oxymethyl]phenyl]-2,2,2-trifluoroethanone

1.2 Other means of identification

Product number -
Other names [(4-(Trifluoroacetyl)benzyl)oxy](-butyl)dimethylsilane

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:87736-75-2 SDS

87736-75-2Relevant articles and documents

SMALL MOLECULE MODULATORS OF PCSK9 AND METHODS OF USE THEREOF

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Paragraph 0367, (2016/02/22)

A compound of Formula (I): or a pharmaceutically acceptable salt, hydrate, solvate, or racemic mixture or stereoisomer thereof, and methods for preventing or treating an LDL-cholesterol-related disease or disorder using such compound(s), and kits and comp

NOVEL N-BENZYLAMIDE SUBSTITUTED DERIVATIVES OF 2-(ACYLAMIDO)ACETIC ACID AND 2-(ACYLAMIDO)PROPIONIC ACIDS: POTENT NEUROLOGICAL AGENTS

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Page/Page column 62-63, (2009/12/27)

A first aspect of the invention is a compound (sometimes also referred to herein as an "active agent" or "active compound") of Formula (I) or ( Ia): or a pharmaceutically acceptable salt or prodrug thereof. Compositions thereof and methods of using the same (e.g. for the treatment of a neurological disease) are also described.

Synthesis of photoactive α-mannosides and mannosyl peptides and their evaluation for lectin labeling

Wiegand, Michaela,Lindhorst, Thisbe K.

, p. 4841 - 4851 (2007/10/03)

Adhesion to the glycosylated surface of eukaryotic cells, mediated by lectins for example, plays an important role in inflammation and other cellular processes of living organisms. To elucidate the mechanisms involved in the adhesion to cell surfaces and

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