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1204234-60-5

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1204234-60-5 Usage

General Description

1-(5-bromopyridin-3-yl)-2,2,2-trifluoroethanol is a chemical compound with the molecular formula C7H6BrF3NO. It is a derivative of pyridine, a colorless and flammable liquid, and is commonly used as a reagent in organic synthesis. 1-(5-broMopyridin-3-yl)-2,2,2-trifluoroethanol is a trifluoroethanol derivative with a bromine-substituted pyridine ring, making it useful for various chemical reactions and as an intermediate in the pharmaceutical industry. Its trifluoroethanol group makes it a potent solvent and it is often used in research laboratories and industry settings for its unique chemical properties. As with any chemical, proper handling and precautions should be taken to ensure safe use of 1-(5-bromopyridin-3-yl)-2,2,2-trifluoroethanol.

Check Digit Verification of cas no

The CAS Registry Mumber 1204234-60-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,4,2,3 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1204234-60:
(9*1)+(8*2)+(7*0)+(6*4)+(5*2)+(4*3)+(3*4)+(2*6)+(1*0)=95
95 % 10 = 5
So 1204234-60-5 is a valid CAS Registry Number.

1204234-60-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(5-bromopyridin-3-yl)-2,2,2-trifluoroethanol

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

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

More Details:1204234-60-5 SDS

1204234-60-5Relevant articles and documents

AZA-HETEROARYL COMPOUNDS AS PI3K-GAMMA INHIBITORS

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Paragraph 0486, (2016/09/12)

The present invention provides aza-heteroaryl derivatives of Formula I: and pharmaceutically acceptable salts thereof, wherein X, Y, Z, A, W, R4, R5, and R6 are defined herein, that inhibit the activity of phosphoinositide 3-kinases-gamma (PI3Kγ) and are useful in the treatment of diseases related to the activity of PI3Kγ including, for example, autoimmune diseases, cancer, cardiovascular diseases, and neurodegenerative diseases.

ALDOSTERONE SYNTHASE INHIBITORS

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Paragraph 0631, (2014/11/11)

The present invention relates to compounds of formula (I): and pharmaceutically acceptable salts thereof, wherein R1, R2. R3, R4, R5, R6, R7, W, Y, m and n are as defined herein. The invention also relates to pharmaceutical compositions comprising these compounds, methods of using these compounds in the treatment of various diseases and disorders, processes for preparing these compounds and intermediates useful in these processes.

Highly efficient synthesis of aryl and heteroaryl trifluoromethyl ketones via o-iodobenzoic acid (IBX)

Cheng, Huicheng,Pei, Yu,Leng, Faqiang,Li, Jingya,Liang, Apeng,Zou, Dapeng,Wu, Yangjie,Wu, Yusheng

, p. 4483 - 4486 (2013/07/26)

A two-step process for the synthesis of aryl and heteroaryl trifluoromethyl ketones from the corresponding aldehydes is described. Trifluoromethyl alcohols were prepared from aryl and heteroaryl aldehydes in excellent yields using catalytic amount of K2CO3. The trifluoromethyl alcohols were then oxidized conveniently and efficiently by o-iodoxybenzoic acid (IBX) under mild conditions to get the desired functionalized aryl and heteroaryl trifluoromethyl ketones.

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