177366-89-1 Usage
Uses
Used in Organic Synthesis:
cis-N-(3-hydroxycyclohexyl)benzamide is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for a wide range of chemical reactions, including nucleophilic substitution, electrophilic addition, and rearrangement reactions. This versatility makes it a valuable building block for the development of new pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
cis-N-(3-hydroxycyclohexyl)benzamide is used as a starting material for the synthesis of various pharmaceutical compounds. Its ability to form stable amide linkages and its reactivity with other functional groups make it an ideal candidate for the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Industry:
cis-N-(3-hydroxycyclohexyl)benzamide is used as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its unique chemical properties enable the development of novel active ingredients with enhanced performance and reduced environmental impact.
Used in Specialty Chemicals:
cis-N-(3-hydroxycyclohexyl)benzamide is used in the production of specialty chemicals, such as dyes, fragrances, and flavorings. Its ability to participate in various chemical reactions allows for the creation of new compounds with unique properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 177366-89-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,3,6 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 177366-89:
(8*1)+(7*7)+(6*7)+(5*3)+(4*6)+(3*6)+(2*8)+(1*9)=181
181 % 10 = 1
So 177366-89-1 is a valid CAS Registry Number.
177366-89-1Relevant articles and documents
Resolution of trans-3-aminocyclohexanol
Bernardelli, Patrick,Bladon, Michael,Lorthiois, Edwige,Manage, Ajith C.,Vergne, Fabrice,Wrigglesworth, Roger
, p. 1451 - 1455 (2007/10/03)
(R,R)- and (S,S)-trans-3-Aminocyclohexanol were prepared via an enzymatic resolution of (±)-trans-1-acetoxy-3-benzylamido-cyclohexane with >95% enantiomeric excess.
Reactions of 1-acylamino-1-(trimethylsiloxy)alkanes: Versatile precursors to acylimines
Johnson, A. Peter,Luke, Richard W. A.,Boa, Andrew N.
, p. 895 - 905 (2007/10/03)
1-Acylamino-1-(trimethylsiloxy)alkanes react with carbon and heteroatom nucleophiles to give the corresponding 1-substituted-1-acylaminoalkanes. The 1-acylamino-1-(trimethylsiloxy)alkanes can also give rise to enamides, and by this route the mild antibiotic tuberin, and the isomeric (Z)-tuberin have been prepared. A further example of their reactions is illustrated with the acid-catalysed intramolecular cyclisation onto a carbon-carbon double bond. These transformations show that 1-acylamino-1-(trimethylsiloxy)alkanes are versatile precursors to synthetically useful acylimines.
