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19064-24-5

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19064-24-5 Usage

Uses

Different sources of media describe the Uses of 19064-24-5 differently. You can refer to the following data:
1. 1,3-Difluoro-2-nitrobenzene is a useful chemical reagent.
2. 2,6-Difluoronitrobenzene may be used in the preparation of secondary amine precursors, required for the synthesis of two families of nitric oxide donors.

Chemical Properties

Light yellow to dark yellow solid

General Description

2,6-Difluoronitrobenzene is an organic building block. Molecular structure, conformation and potential to internal rotation of 2,6-difluoronitrobenzene been studied by gas-phase electron diffraction (GED), MP2 ab initio, and by B3LYP density functional calculations.

Check Digit Verification of cas no

The CAS Registry Mumber 19064-24-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,6 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19064-24:
(7*1)+(6*9)+(5*0)+(4*6)+(3*4)+(2*2)+(1*4)=105
105 % 10 = 5
So 19064-24-5 is a valid CAS Registry Number.
InChI:InChI=1/CH3NO.F6P/c1-2-3;1-7(2,3,4,5)6/h2H,1H2;/q+1;-1

19064-24-5 Well-known Company Product Price

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  • (Code)Product description
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  • Aldrich

  • (382957)  2,6-Difluoronitrobenzene  98%

  • 19064-24-5

  • 382957-1G

  • 931.32CNY

  • Detail
  • Aldrich

  • (382957)  2,6-Difluoronitrobenzene  98%

  • 19064-24-5

  • 382957-5G

  • 3,223.35CNY

  • Detail

19064-24-5SDS

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 1,3-difluoro-2-nitrobenzene

1.2 Other means of identification

Product number -
Other names 2,6-fluoronitrobenzene

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:19064-24-5 SDS

19064-24-5Relevant articles and documents

Pseudocyclic bis-N-heterocycle-stabilized iodanes - synthesis, characterization and applications

Boelke, Andreas,Lork, Enno,Nachtsheim, Boris J.,Sadat, Soleicha

supporting information, p. 7434 - 7437 (2021/08/03)

Bis-N-heterocycle-stabilized λ3-iodanes (BNHIs) based on azoles are introduced as novel structural motifs in hypervalent iodine chemistry. A performance test in a variety of benchmark reactions including sulfoxidations and phenol dearomatizations revealed a bis-N-bound pyrazole substituted BNHI as the most reactive derivative. Its solid-state structure was characterizedviaX-ray analysis implying strong intramolecular interactions between the pyrazole nitrogen atoms and the hypervalent iodine centre.

DIHYDROBENZOFURANYL DERIVATIVES AND METHODS OF THEIR USE

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Page/Page column 20, (2008/12/06)

The present invention is directed to dihydrobenzofuranyl derivatives of formula I: or a pharmaceutically acceptable salt thereof, which are monoamine reuptake inhibitors, compositions containing these derivatives, and methods of their use for the prevention and treatment of conditions, including, inter alia, vasomotor symptoms sexual dysfunction, gastrointestinal disorders and genitourinary disorder, depression disorders, endogenous behavioral disorder, cognitive disorder, diabetic neuropathy, pain, and other diseases or disorders.

Progesterone receptor antagonists, contraceptive regimens, and kits

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Page/Page column 8, (2010/02/15)

A method of contraception is provided which involves delivery of 21 to 27 consecutive days of one or more PR antagonists in the absence of a progestin, estrogen, or other steroidal compound, followed by 1 to 7 days without any active agent. Also described is a pharmaceutically useful kit to facilitate delivery of this regimen.

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