2164-37-6 Usage
Uses
Used in Organic Synthesis:
(6,7-dichloro-2,3-dihydro-1,4-benzodioxin-2-yl)methanol is utilized as a key intermediate in organic synthesis, serving as a building block for the production of a variety of chemicals. Its reactivity, stemming from the chlorine atoms on the benzene ring, allows for the introduction of specific functionalities into organic molecules, facilitating the creation of diverse chemical products.
Used in Chemical Reactions:
(6,7-dichloro-2,3-dihydro-1,4-benzodioxin-2-yl)methanol is also employed in various chemical reactions to introduce desired functional groups into target molecules. The presence of chlorine atoms on the benzene ring enhances its reactivity, making it a suitable candidate for such transformations and broadening its applicability in the field of chemistry.
Used in Pharmaceutical Research:
(6,7-dichloro-2,3-dihydro-1,4-benzodioxin-2-yl)methanol has been studied for its potential biological activities and pharmacological properties. Its unique structure and reactivity make it a promising candidate for the development of new drugs and therapeutic agents, particularly in the areas of medicinal chemistry and drug design.
Used in the Chemical Industry:
In the chemical industry, (6,7-dichloro-2,3-dihydro-1,4-benzodioxin-2-yl)methanol is used as a starting material for the synthesis of various specialty chemicals, including those with applications in materials science, agrochemicals, and other industrial sectors. Its versatility and reactivity contribute to its value as a synthetic intermediate in this domain.
Check Digit Verification of cas no
The CAS Registry Mumber 2164-37-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,6 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2164-37:
(6*2)+(5*1)+(4*6)+(3*4)+(2*3)+(1*7)=66
66 % 10 = 6
So 2164-37-6 is a valid CAS Registry Number.
2164-37-6Relevant academic research and scientific papers
3-(Benzodioxan-2-ylmethoxy)-2,6-difluorobenzamides bearing hydrophobic substituents at the 7-position of the benzodioxane nucleus potently inhibit methicillin-resistant Sa and Mtb cell division
Straniero, Valentina,Pallavicini, Marco,Chiodini, Giuseppe,Zanotto, Carlo,Volontè, Luca,Radaelli, Antonia,Bolchi, Cristiano,Fumagalli, Laura,Sanguinetti, Maurizio,Menchinelli, Giulia,Delogu, Giovanni,Battah, Basem,De Giuli Morghen, Carlo,Valoti, Ermanno
, p. 227 - 243 (2016/05/24)
Lipophilic substituents at benzodioxane C (7) of 3-(benzodioxan-2-ylmethoxy)-2,6-difluorobenzamide improve the antibacterial activity against methicillin-resistant Staphylococcus aureus strains to MIC values in the range of 0.2-2.5 μg/mL, whereas hydrophi
