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124700-41-0

124700-41-0

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124700-41-0 Usage

Chemical Properties

White solid

Uses

2-Fluoro-5-iodobenzoic acid is one of the precursor molecules were shown to generate ETD reagents via ESI followed by CID. Starting material in the synthesis of 3, 6-disubstituted 2-pyridinecarboxamide(GK activators).

Check Digit Verification of cas no

The CAS Registry Mumber 124700-41-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,7,0 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 124700-41:
(8*1)+(7*2)+(6*4)+(5*7)+(4*0)+(3*0)+(2*4)+(1*1)=90
90 % 10 = 0
So 124700-41-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H4FIO2/c8-6-2-1-4(9)3-5(6)7(10)11/h1-3H,(H,10,11)

124700-41-0 Well-known Company Product Price

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  • Alfa Aesar

  • (H26175)  2-Fluoro-5-iodobenzoic acid, 97%   

  • 124700-41-0

  • 1g

  • 602.0CNY

  • Detail

  • Alfa Aesar

  • (H26175)  2-Fluoro-5-iodobenzoic acid, 97%   

  • 124700-41-0

  • 5g

  • 1883.0CNY

  • Detail

124700-41-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Fluoro-5-iodobenzoic acid

1.2 Other means of identification

Product number -
Other names 2-Fluoro-5-iodobenzoic 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:124700-41-0 SDS

124700-41-0Relevant articles and documents

Synthesis method of 2-halogen-5-iodobenzoic acid

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Paragraph 0043-0047, (2019/09/17)

The invention discloses a synthesis method of 2-halogen-5-iodobenzoic acid. The synthesis method comprises steps as follows: o-halogen benzoic acids are subjected to one-step iodo treatment in an iodio reagent, and 2-halogen-5-iodobenzoic acid is obtained. Aftertreatment comprises steps as follows: a reaction liquid is poured into a cold reductive water solution and quenched, a solvent is evaporated to dryness, recrystallization and filtration are performed, and a product can be obtained. The method is short in reaction route, simple to operate, environmentally friendly, safer and more economical and has broad application prospects.

Novel HIV-1 integrase inhibitors derived from quinolone antibiotics

Sato, Motohide,Motomura, Takahisa,Aramaki, Hisateru,Matsuda, Takashi,Yamashita, Masaki,Ito, Yoshiharu,Kawakami, Hiroshi,Matsuzaki, Yuji,Watanabe, Wataru,Yamataka, Kazunobu,Ikeda, Satoru,Kodama, Eiichi,Matsuoka, Masao,Shinkai, Hisashi

, p. 1506 - 1508 (2007/10/03)

The viral enzyme integrase is essential for the replication of human immunodeficiency virus type 1 (HIV-1) and represents a remaining target for antiretroviral drugs. Here, we describe the modification of a quinolone antibiotic to produce the novel integr

4-oxo-1,4-dihydro-3-cinnolinecarboxamides as antiviral agents

-

, (2008/06/13)

This invention provides compounds of formula I; which are useful as antiviral agents.

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