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182344-25-8

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182344-25-8 Usage

Chemical Properties

White solid

Check Digit Verification of cas no

The CAS Registry Mumber 182344-25-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,3,4 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 182344-25:
(8*1)+(7*8)+(6*2)+(5*3)+(4*4)+(3*4)+(2*2)+(1*5)=128
128 % 10 = 8
So 182344-25-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H8BFO2/c12-10-6-5-9(11(13)14)7-3-1-2-4-8(7)10/h1-6,13-14H

182344-25-8 Well-known Company Product Price

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

  • (F1080)  4-Fluoro-1-naphthaleneboronic Acid (contains varying amounts of Anhydride)  

  • 182344-25-8

  • 200mg

  • 350.00CNY

  • Detail
  • TCI America

  • (F1080)  4-Fluoro-1-naphthaleneboronic Acid (contains varying amounts of Anhydride)  

  • 182344-25-8

  • 1g

  • 1,250.00CNY

  • Detail
  • Alfa Aesar

  • (H52707)  4-Fluoronaphthalene-1-boronic acid, 98%   

  • 182344-25-8

  • 250mg

  • 882.0CNY

  • Detail
  • Alfa Aesar

  • (H52707)  4-Fluoronaphthalene-1-boronic acid, 98%   

  • 182344-25-8

  • 1g

  • 2822.0CNY

  • Detail

182344-25-8SDS

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-fluoronaphthalen-1-yl)boronic acid

1.2 Other means of identification

Product number -
Other names 4-fluoro-1-naphthylboronic 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:182344-25-8 SDS

182344-25-8Relevant articles and documents

4-fluoronaphthalene-1-alcohol preparation technology

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Paragraph 0043; 0044; 0045; 0067; 0068; 0069, (2017/08/26)

The invention discloses a 4-fluoronaphthalene-1-alcohol preparation technology. The preparation technology takes 1-fluoronaphthalene as a raw material, the raw material is subjected to halogenation, boration and hydrolysis to obtain the 4-fluoronaphthalene-1-alcohol, and the overall yield can reach 60%. The technology has the advantages of low cost and easy acquisition of the raw materials, simple and easy operation of post-treatment t, high yield, and easy industrial application.

Structure-Activity Relationships of Potent, Selective Inhibitors of Neuronal Nitric Oxide Synthase Based on the 6-Phenyl-2-aminopyridine Structure

Lowe III, John A.,Qian, Weimin,Drozda, Susan E.,Volkmann, Robert A.,Nason, Deane,Nelson, Robert B.,Nolan, Charles,Liston, Dane,Ward, Karen,Faraci, Steve,Verdries, Kim,Seymour, Pat,Majchrzak, Michael,Villalobos, Anabella,White, W. Frost

, p. 1575 - 1586 (2007/10/03)

The synthesis and structure-activity relationships of a series of 6-phenyl-2-aminopyridines that potently and selectively inhibit the neuronal isoform of nitric oxide synthase (nNOS) are described. Compound 14bi from this series exhibits potent in vivo activity in harmaline-induced cGMP formation in rat cerebellum, a functional model of nNOS inhibition, and in the PCP-induced hypermotility model in the rat. These results suggest that 14bi may be a useful reagent for evaluating potential therapeutic applications of nNOS inhibitors in the central nervous system.

2-aminopyridines containing fused ring substituents

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, (2008/06/13)

The present invention relates to 2-aminopyridine derivatives of the formula wherein G, R1 and R2 are defined as in the specification, that exhibit activity as nitric oxide synthase (NOS) inhibitors, to pharmaceutical compositions containing them and to their use in the treatment and prevention of central nervous system and other disorders.

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