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883107-68-4

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883107-68-4 Usage

General Description

6-Chloro-2-fluoro-3-hydroxypyridine is a type of compound classified under the chemical category of organohalogens. Organohalogens are organic compounds which contain at least one halogen (fluorine, chlorine, bromine, iodine, astatine) atom. In the name, "6-Chloro" indicates the presence of a Chlorine atom, "2-Fluoro" denotes a Fluorine atom, and "3-hydroxypyridine" suggests the presence of a Hydroxy group (-OH) attached to a pyridine ring. It is typically used in pharmaceuticals and chemical research applications. Careful handling of this compound is necessary due to its possibly reactive nature, though specific properties, applications, and health effects may vary based on its application and concentration.

Check Digit Verification of cas no

The CAS Registry Mumber 883107-68-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,3,1,0 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 883107-68:
(8*8)+(7*8)+(6*3)+(5*1)+(4*0)+(3*7)+(2*6)+(1*8)=184
184 % 10 = 4
So 883107-68-4 is a valid CAS Registry Number.

883107-68-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-2-fluoropyridin-3-ol

1.2 Other means of identification

Product number -
Other names 2-FLUORO-6-CHLORO-3-HYDROXYPYRIDINE

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:883107-68-4 SDS

883107-68-4Relevant articles and documents

BIARYL KINASE INHIBITORS

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Page/Page column 138; 139, (2017/05/07)

The present disclosure is directed to biaryl compounds of formula (I) which can inhibit AAKl (adaptor associated kinase 1), compositions comprising such compounds and their use for treating e.g. pain, Alzheimer's disease, Parkinson's disease and schizophrenia.

An orally available BACE1 inhibitor that affords robust CNS Aβ reduction without cardiovascular liabilities

Cheng, Yuan,Brown, James,Judd, Ted C.,Lopez, Patricia,Qian, Wenyuan,Powers, Timothy S.,Chen, Jian Jeffrey,Bartberger, Michael D.,Chen, Kui,Dunn, Robert T.,Epstein, Oleg,Fremeau, Robert T.,Harried, Scott,Hickman, Dean,Hitchcock, Stephen A.,Luo, Yi,Minatti, Ana Elena,Patel, Vinod F.,Vargas, Hugo M.,Wahl, Robert C.,Weiss, Matthew M.,Wen, Paul H.,White, Ryan D.,Whittington, Douglas A.,Zheng, Xiao Mei,Wood, Stephen

supporting information, p. 210 - 215 (2015/03/04)

BACE1 inhibition to prevent Aβ peptide formation is considered to be a potential route to a disease-modifying treatment for Alzheimer's disease. Previous efforts in our laboratory using a combined structure- and property-based approach have resulted in th

AMINO -DIHYDROOXAZINE AND AMINO - DIHYDROTHIAZINE SPIRO COMPOUNDS AS BETA - SECRETASE MODULATORS AND THEIR MEDICAL USE

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Page/Page column 59, (2011/10/10)

The present invention comprises a new class of compounds useful for the modulation of Beta-secretase enzyme activity and for the treatment of Beta-secretase mediated diseases, including Alzheimer's disease (AD) and related conditions. In one embodiment, the compounds have a general Formula (I): wherein A1, A2, A3, A4, A5, A6, R2, R7, X, Y and Z of Formula (I) are defined herein. The invention also includes use of these compounds in pharmaceutical compositions for treatment, prophylactic or therapeutic, of disorders and conditions related to the activity of beta-secretase protein. Such disorders include, for example, Alzheimer's Disease, cognitive deficits, cognitive impairment, schizophrenia and other central nervous system conditions related to and/or caused by the formation and/or deposition of plaque on the brain. The invention also comprises further embodiments of Formula (I), intermediates and processes useful for the preparation of compounds of Formula (I).

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