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179897-94-0

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179897-94-0 Usage

Chemical Properties

White to off-white powder

Uses

Different sources of media describe the Uses of 179897-94-0 differently. You can refer to the following data:
1. 5-Fluoro-2-methoxyphenylboronic Acid is an important building blocks in organic syntheses. A reagent for Suzuki coupling reactions and copper catalyzed arylation reactions. A bacterial mutagen.
2. Reactant for:? ;Suzuki couplings1,2? ;Copper catalyzed arylation3
3. suzuki reaction

Check Digit Verification of cas no

The CAS Registry Mumber 179897-94-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,8,9 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 179897-94:
(8*1)+(7*7)+(6*9)+(5*8)+(4*9)+(3*7)+(2*9)+(1*4)=230
230 % 10 = 0
So 179897-94-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H6BFO3/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3,9-11H

179897-94-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (F0775)  5-Fluoro-2-methoxyphenylboronic Acid (contains varying amounts of Anhydride)  

  • 179897-94-0

  • 5g

  • 390.00CNY

  • Detail
  • TCI America

  • (F0775)  5-Fluoro-2-methoxyphenylboronic Acid (contains varying amounts of Anhydride)  

  • 179897-94-0

  • 25g

  • 1,540.00CNY

  • Detail
  • Alfa Aesar

  • (H32748)  5-Fluoro-2-methoxybenzeneboronic acid, 98%   

  • 179897-94-0

  • 5g

  • 424.0CNY

  • Detail
  • Alfa Aesar

  • (H32748)  5-Fluoro-2-methoxybenzeneboronic acid, 98%   

  • 179897-94-0

  • 25g

  • 1623.0CNY

  • Detail

179897-94-0SDS

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 (5-fluoro-2-methoxyphenyl)boronic acid

1.2 Other means of identification

Product number -
Other names 2-Methoxy-5-fluorophenylboronic acid

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:179897-94-0 SDS

179897-94-0Relevant articles and documents

HALOGENATED CATALYSTS COMPRISING SALAN LIGANDS

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Page/Page column 47; 48, (2014/02/16)

Catalysts comprising a halogenated Salan ligand. Also disclosed are catalyst systems comprising the catalyst and an activator; methods to prepare the ligands, catalysts and catalyst systems; processes to polymerize olefins using the catalysts and/or catalyst systems; and the olefin polymers prepared according to the processes.

Substituted 3-amino biaryl propionic acids as potent VLA-4 antagonists.

Kopka, Ihor E,Lin, Linus S,Mumford, Richard A,Lanza Jr., Thomas,Magriotis, Plato A,Young, David,DeLaszlo, Stephen E,MacCoss, Malcolm,Mills, Sander G,Van Riper, Gail,McCauley, Ermengilda,Lyons, Kathryn,Vincent, Stella,Egger, Linda A,Kidambi, Usha,Stearns, Ralph,Colletti, Adria,Teffera, Yohannes,Tong, Sharon,Owens, Karen,Levorse, Dorothy,Schmidt, John A,Hagmann, William K

, p. 2415 - 2418 (2007/10/03)

A series of substituted N-(3,5-dichlorobenzenesulfonyl)-(L)-prolyl- and (L)-azetidyl-beta-biaryl beta-alanine derivatives was prepared as selective and potent VLA-4 antagonists. The 2,6-dioxygenated biaryl substitution pattern is important for optimizing potency. Oral bioavailability was variable and may be a result of binding to circulating plasma proteins.

STEROID RECEPTOR MODULATOR COMPOUNDS AND METHODS

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, (2008/06/13)

Non-steroidal compounds which are high affinity, high selectivity modulators for steroid receptors are disclosed. Also disclosed are pharmaceutical compositions incorporating such compounds, methods for employing the disclosed compounds and compositions for treating patients requiring steroid receptor agonist or antagonist therapy, intermediates useful in the preparation of the compounds and processes for the preparation of the steroid receptor modulator compounds.

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