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Silane, (4-bromo-2,6-dimethylphenoxy)(1,1-dimethylethyl)dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

139229-99-5

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139229-99-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 139229-99-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,2,2 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 139229-99:
(8*1)+(7*3)+(6*9)+(5*2)+(4*2)+(3*9)+(2*9)+(1*9)=155
155 % 10 = 5
So 139229-99-5 is a valid CAS Registry Number.

139229-99-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-bromo-2,6-dimethylphenoxy)-tert-butyl-dimethylsilane

1.2 Other means of identification

Product number -
Other names Silane,(4-bromo-2,6-dimethylphenoxy)(1,1-dimethylethyl)dimethyl

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:139229-99-5 SDS

139229-99-5Relevant academic research and scientific papers

Design, synthesis and evaluation of potent G-protein coupled receptor 40 agonists

Huang, Jing,Guo, Bin,Chu, Wen-Jing,Xie, Xin,Yang, Yu-She,Zhou, Xian-Li

, p. 159 - 162 (2016)

GPR40 has emerged as an attractive drug target for the treatment of type 2 diabetes due to its role in the enhancement of insulin secretion with glucose dependency. With the aim to improve the metabolic and safety profiles, a series of novel phenylpropionic acid derivatives were synthesized. Extensive structural optimization led to identification of compounds 22g and 23e as potent GPR40 agonists with moderate liver microsomal stability. All the discovery supported further exploration surrounding this scaffold.

LIPID PRODRUGS OF NEUROSTEROIDS

-

Paragraph 00462-00463, (2021/08/13)

The present invention provides lymphatic system-directing lipid prodrugs, pharmaceutical compositions thereof, methods of producing such prodrugs and compositions, as well as methods of improving the bioavailability or other properties of a therapeutic agent that comprises part of the lipid prodrug. The present invention also provides methods of treating a disease, disorder, or condition such as those disclosed herein, comprising administering to a patient in need thereof a disclosed lipid prodrug or a pharmaceutical composition thereof.

Organic synthesis using a hypervalent iodine reagent: Unexpected and novel domino reaction leading to spiro cyclohexadienone lactones

Fujioka, Hiromichi,Komatsu, Hideyuki,Nakamura, Taeko,Miyoshi, Akihito,Hata, Kayoko,Ganesh, Jnashuara,Murai, Kenichi,Kita, Yasuyuki

supporting information; scheme or table, p. 4133 - 4135 (2010/09/03)

The reaction of 1-(p-hydroxyaryl)cyclobutanols and phenyl iodide(iii) diacetate in hexafluoroisopropanol and water produced spiro cyclohexadienone lactones via a domino reaction.

A dual sensor spin trap for use with EPR spectroscopy

Caldwell, Stuart T.,Quin, Caroline,Edge, Ruth,Hartley, Richard C.

, p. 3499 - 3502 (2008/02/12)

Redox active metal ions, carbon-centered radicals, and oxygen-centered radicals are important to oxidative stress. A radical detector combining a nitrone spin trap, a phenol, and a cyclopropane radical clocklike unit was prepared and used with EPR spectroscopy to detect and distinguish between hydroxyl radicals, methyl radicals, and iron(III) ions. Iron(III) reacts with the phenol unit inducing opening of the cyclopropane ring and cyclization to generate a stable nitroxyl radical.

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