1645-96-1 Usage
Uses
Used in Organic Synthesis:
2,2-DIFLUORO-5-NITRO-1,3-BENZODIOXOLE is used as a key intermediate in organic synthesis for the production of a variety of organic compounds. Its unique structure allows for the creation of diverse chemical entities, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2,2-DIFLUORO-5-NITRO-1,3-BENZODIOXOLE is utilized as a building block for the development of new pharmaceuticals. Its presence in the molecular structure can influence the pharmacokinetics and pharmacodynamics of drug candidates, potentially leading to more effective and safer medications.
Used in Agrochemical Development:
2,2-DIFLUORO-5-NITRO-1,3-BENZODIOXOLE is also employed in the research and development of agrochemicals. Its incorporation into the molecular structures of these compounds can enhance their efficacy against pests and diseases, contributing to more effective crop protection strategies.
Used as an Antibacterial Agent:
Due to its potent biological activity, 2,2-DIFLUORO-5-NITRO-1,3-BENZODIOXOLE has been studied for its potential as an antibacterial agent. Its ability to target and inhibit bacterial growth makes it a candidate for the development of new antibiotics to combat resistant strains.
Used as an Antifungal Agent:
Similarly, 2,2-DIFLUORO-5-NITRO-1,3-BENZODIOXOLE has been investigated for its antifungal properties. Its application in antifungal agents could provide new treatment options for fungal infections, addressing the need for novel antifungal therapies.
Used in Industrial Applications:
The presence of fluorine atoms in 2,2-DIFLUORO-5-NITRO-1,3-BENZODIOXOLE may confer unique physical and chemical properties that are advantageous in industrial applications. These properties can be harnessed to improve the performance of materials and processes in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1645-96-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,4 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1645-96:
(6*1)+(5*6)+(4*4)+(3*5)+(2*9)+(1*6)=91
91 % 10 = 1
So 1645-96-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H3F2NO4/c8-7(9)13-5-2-1-4(10(11)12)3-6(5)14-7/h1-3H
1645-96-1Relevant academic research and scientific papers
Bactericide and application thereof
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Paragraph 0050; 0051; 0052, (2019/01/23)
The invention relates to the technical field of agriculture, in particular to a bactericide. The bactericide comprises a compound in a formula (A) as shown in the specification, wherein X1 and X2 areselected from fluorine and chlorine and can be identical or different, R1 and R2 are selected from aliphatic alkyls in carbon number of 1-20 and aryls formed by carbon and hydrogen and in carbon number of 6-20, and R is selected from aliphatic alkyls in carbon number of 1-20.
Bactericide and application thereof
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Paragraph 0043-0046, (2019/02/03)
The invention relates to the technical field of agriculture, in particular to a bactericide. The bactericide comprises a compound show as the formula (A) (as described in the specification), wherein X1 and X2 are selected from fluorine and chlorine, and X1 and X2 can be same or different; and R1 and R2 are selected from aliphatic alkyl groups with 1 to 20 carbon atoms, and aryl groups (comprisingcarbon and hydrogen) with 6 to 20 carbon atoms.
Sterilizing agent and application thereof
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Paragraph 0043-0045, (2019/01/13)
The invention relates to the technical field of agriculture, in particular to a sterilizing agent. The sterilizing agent comprises a compound as shown in formula (A): (shown in the description), wherein X1 and X2 are selected from fluorine; and R1 and R2 are selected from methyl, ethyl, propyl, butyl, amyl, hexyl and phenyl.
Constructing the OCF2O moiety using BrF3
Hagooly, Youlia,Rozen, Shlomo
, p. 6780 - 6783 (2008/12/22)
(Chemical Equation Presented) A general preparation for aromatic and aliphatic, cyclic as well as linear, symmetric and asymmetric difluoromethylenedioxy derivatives is described. The alcohols were reacted with thiophosgene to give thiocarbonates, which in turn were reacted with BrF 3. The fluorination step is complete in seconds with moderate to high yields under mild conditions.
