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1072945-00-6

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1072945-00-6 Usage

General Description

2,6-Difluoropyridine-3-boronic acid, pinacol ester is a chemical compound commonly used in organic synthesis and pharmaceutical research. It is a boronic acid derivative, which makes it a valuable building block for the synthesis of various biologically active molecules and pharmaceutical drugs. The pinacol ester group attached to the boronic acid functionality provides enhanced stability and reactivity, making it a versatile reagent for cross-coupling reactions and other organic transformations. Its unique fluorinated pyridine core also makes it a useful tool in medicinal chemistry for the development of new drugs with improved properties and activities. Overall, 2,6-difluoropyridine-3-boronic acid, pinacol ester is an important chemical compound with a wide range of applications in the fields of organic synthesis and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 1072945-00-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,2,9,4 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1072945-00:
(9*1)+(8*0)+(7*7)+(6*2)+(5*9)+(4*4)+(3*5)+(2*0)+(1*0)=146
146 % 10 = 6
So 1072945-00-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H14BF2NO2/c1-10(2)11(3,4)17-12(16-10)7-5-6-8(13)15-9(7)14/h5-6H,1-4H3

1072945-00-6 Well-known Company Product Price

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  • Alfa Aesar

  • (H26965)  2,6-Difluoropyridine-3-boronic acid pinacol ester, 95%   

  • 1072945-00-6

  • 250mg

  • 1725.0CNY

  • Detail
  • Alfa Aesar

  • (H26965)  2,6-Difluoropyridine-3-boronic acid pinacol ester, 95%   

  • 1072945-00-6

  • 1g

  • 3989.0CNY

  • Detail

1072945-00-6SDS

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 2,6-difluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

1.2 Other means of identification

Product number -
Other names 2,5-DIFLUOROBENZOTRIFLUORIDE

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:1072945-00-6 SDS

1072945-00-6Downstream Products

1072945-00-6Relevant articles and documents

Identification of Potent and Selective RIPK2 Inhibitors for the Treatment of Inflammatory Diseases

He, Xiaohui,Da Ros, Sara,Nelson, John,Zhu, Xuefeng,Jiang, Tao,Okram, Barun,Jiang, Songchun,Michellys, Pierre-Yves,Iskandar, Maya,Espinola, Sheryll,Jia, Yong,Bursulaya, Badry,Kreusch, Andreas,Gao, Mu-Yun,Spraggon, Glen,Baaten, Janine,Clemmer, Leah,Meeusen, Shelly,Huang, David,Hill, Robert,Nguyen-Tran, Van,Fathman, John,Liu, Bo,Tuntland, Tove,Gordon, Perry,Hollenbeck, Thomas,Ng, Kenneth,Shi, Jian,Bordone, Laura,Liu, Hong

, p. 1048 - 1053 (2017)

NOD2 (nucleotide-binding oligomerization domain-containing protein 2) is an internal pattern recognition receptor that recognizes bacterial peptidoglycan and stimulates host immune responses. Dysfunction of NOD2 pathway has been associated with a number of autoinflammatory disorders. To date, direct inhibitors of NOD2 have not been described due to technical challenges of targeting the oligomeric protein complex. Receptor interacting protein kinase 2 (RIPK2) is an intracellular serine/threonine/tyrosine kinase, a key signaling partner, and an obligate kinase for NOD2. As such, RIPK2 represents an attractive target to probe the pathological roles of NOD2 pathway. To search for selective RIPK2 inhibitors, we employed virtual library screening (VLS) and structure based design that eventually led to a potent and selective RIPK2 inhibitor 8 with excellent oral bioavailability, which was used to evaluate the effects of inhibition of RIPK2 in various in vitro assays and ex vivo and in vivo pharmacodynamic models.

INHIBITORS OF THE KYNURENINE PATHWAY

-

Page/Page column 206; 207, (2014/12/12)

The present application provides novel inhibitors of indoleamine 2,3-dioxygenase-1 and/or indoleamine 2,3-dioxygenase-2 and/or tryptophan 2,3-dioxygenase, metabolites thereof, and phannaceutically acceptable salts or prodrugs thereof. Also provided are methods for preparing these compounds. A therapeutically effective amount of one or more of the compounds of formula (I) is useful in treating diseases resulting from dysregulation of the kynurenine pathway. Compounds of formula (I) act by inhibiting the enzymatic activity or expression of indoleamine 2,3-dioxygenase-1 and/or indoleamine 2,3-dioxygenase-2 and/or tryptophan 2,3-dioxygenase.

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