123843-64-1 Usage
Uses
Used in Pharmaceutical Industry:
1-Butoxy-3,5-difluorobenzene is used as a chemical intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and improving the efficacy of existing medications.
Used in Pesticide Industry:
In the pesticide industry, 1-Butoxy-3,5-difluorobenzene is utilized as a key intermediate in the production of effective and environmentally friendly pesticides, enhancing crop protection and yield.
Used in Specialty Chemicals:
1-Butoxy-3,5-difluorobenzene is employed as an intermediate in the manufacturing of specialty chemicals, which are used in a variety of applications such as coatings, adhesives, and sealants, improving their performance and durability.
Used as a Solvent:
1-Butoxy-3,5-difluorobenzene is used as a solvent in various chemical processes, facilitating reactions and improving the efficiency of production.
Used in Flavor and Fragrance Industry:
In the flavor and fragrance industry, 1-Butoxy-3,5-difluorobenzene is utilized in the manufacturing of various products, imparting unique and desirable scents to consumer goods.
Safety Considerations:
While 1-Butoxy-3,5-difluorobenzene is not considered highly toxic, it may cause irritation to the skin, eyes, and respiratory tract upon exposure. Therefore, it is essential to follow proper safety measures when handling and using this chemical to minimize potential health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 123843-64-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,8,4 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 123843-64:
(8*1)+(7*2)+(6*3)+(5*8)+(4*4)+(3*3)+(2*6)+(1*4)=121
121 % 10 = 1
So 123843-64-1 is a valid CAS Registry Number.
123843-64-1Relevant articles and documents
NON-LYSOSOMAL GLUCOSYLCERAMIDASE INHIBITORS AND USES THEREOF
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Paragraph 00298, (2020/12/01)
The invention provides compounds for inhibiting glucosylceramidases, prodrugs of the compounds, and pharmaceutical compositions including the compounds or prodrugs of the compounds.
The Synthesis and Transition Temperatures of Some Fluoro-Substituted 4-Cyanophenyl and 4-Cyanobiphenyl-4'-yl 4-Pentyl- and 4-Butoxy-Benzoates
Gray, G. W.,Hird, M.,Lacey, D.,Toyne, K. J.
, p. 165 - 190 (2007/10/02)
A series of 4-cyanophenyl 4-X-benzoates and a series of 4-cyanobiphenyl-4'-yl 4-X-benzoates (X= pentyl, butoxy) have been prepared without fluoro-substitution and with mono-fluoro to tetra-fluoro-substitution; all possible combinations of substitution patterns at the positions ortho- to the cyano group and ortho- to the carboxylate group have been obtained in an attempt to determine the structural features which are responsible for some members of these series showing very large positive values of dielectric anisotropy.The synthesis of novel precursors required for the preparation of these esters is described and the melting points and transition temperatures of the esters are discussed and an explanation is provided for the variation of Tn-1 values with position and extent of fluoro-substitution. - Keywords: Fluoro-substitution, phenyl and biphenyl benzoates, terminal cyano namatogens.
