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67226-78-2

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67226-78-2 Usage

Description

Ethyl [(tert-Butyldimethylsilyl)oxy]acetate, with the CAS number 67226-78-2, is a colorless oil compound that is primarily utilized in the field of organic synthesis. Its unique chemical structure allows it to serve as a versatile building block for the creation of various complex organic molecules.

Uses

Used in Organic Synthesis:
Ethyl [(tert-Butyldimethylsilyl)oxy]acetate is used as a synthetic intermediate for the development of a wide range of organic compounds. Its application in this field is due to its ability to facilitate the formation of new chemical bonds and reactions, leading to the creation of diverse molecules with potential applications in various industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Ethyl [(tert-Butyldimethylsilyl)oxy]acetate is used as a key component in the synthesis of various drugs and drug candidates. Its role in this industry is attributed to its ability to contribute to the development of novel therapeutic agents with improved efficacy and reduced side effects.
Used in Chemical Research:
Ethyl [(tert-Butyldimethylsilyl)oxy]acetate is also employed in chemical research as a valuable tool for understanding the fundamental principles of organic chemistry. Its use in this context is due to its ability to provide insights into the reactivity and behavior of different functional groups and molecular structures.
Used in Material Science:
In the field of material science, Ethyl [(tert-Butyldimethylsilyl)oxy]acetate is used as a precursor for the development of advanced materials with specific properties. Its application in this industry is driven by its potential to contribute to the creation of materials with enhanced performance characteristics, such as improved strength, durability, or chemical resistance.

Check Digit Verification of cas no

The CAS Registry Mumber 67226-78-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,2,2 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 67226-78:
(7*6)+(6*7)+(5*2)+(4*2)+(3*6)+(2*7)+(1*8)=142
142 % 10 = 2
So 67226-78-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H22O3Si/c1-7-12-9(11)8-13-14(5,6)10(2,3)4/h7-8H2,1-6H3

67226-78-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-[tert-butyl(dimethyl)silyl]oxyacetate

1.2 Other means of identification

Product number -
Other names ETHYL [(TERT-BUTYLDIMETHYLSILYL)OXY]ACETATE

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:67226-78-2 SDS

67226-78-2Relevant articles and documents

Hydrophilic azaspiroalkenes as robust bioorthogonal reporters

An, Peng,Wu, Hsuan-Yi,Lewandowski, Tracey M.,Lin, Qing

supporting information, p. 14005 - 14008 (2019/01/03)

Two hydrophilic spiroalkenes, azaspiro[2.3]hex-1-ene and azaspiro[2.4]hept-1-ene, were designed and synthesized. Compared to the previously reported spiro[2.3]hex-1-ene, the azaspiroalkenes exhibited greater water solubility and reactivity as dipolarophiles in the photoinduced tetrazole-alkene cycloaddition reaction. In addition, an azaspiro[2.3]hex-1-ene-containing amino acid, AsphK, was found to be charged by an engineered pyrrolysyl-tRNA synthetase into proteins via amber codon suppression in E. coli as well as in mammalian cells.

Pyrido[1,2-a]pyrimidone analogs as PI3K inhibitors

-

Paragraph 0117; 0122; 0123; 0124, (2016/10/08)

The present invention discloses a class of pyrido[1,2-a]pyrimidone analogs as PI3K inhibitors, and particularly relates to a compound represented by a formula (I) or a pharmaceutically acceptable salt thereof. The formula (I) is defined in the specification.

THIAZOLYL AND OXAZOLYL UREA, THIOUREA, GUANIDINE AND CYANOGUANIDINE COMPOUNDS AS TRKA KINASE INHIBITORS

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Paragraph 00465, (2014/06/11)

Compounds of Formula (I) or stereoisomers, tautomers, or pharmaceutically acceptable salts, solvates or prodrugs thereof, wherein Ring A, Ring C and X are as defined herein, are inhibitors of TrkA kinase and are useful in the treatment of diseases which can be treated with a TrkA kinase inhibitor such as pain, cancer, inflammation, neurodegenerative diseases, certain infectious diseases, Sjogren's syndrome, endometriosis, diabetic peripheral neuropathy, prostatitis or pelvic pain syndrome.

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