90978-87-3 Usage
General Description
N,O-diacetyl-4-aMinocyclohexanol is a chemical compound with the molecular formula C10H15NO3. It is a derivative of cyclohexanol and contains two acetyl groups and one amino group. N,O-diacetyl-4-aMinocyclohexanol is commonly used as an intermediate in the synthesis of various pharmaceuticals, especially in the production of analgesic and antipyretic drugs. N,O-diacetyl-4-aMinocyclohexanol exhibits analgesic properties and has been studied for its potential therapeutic effects in pain relief. It is important for researchers and pharmaceutical manufacturers in the development and production of medications with pain-relieving properties.
Check Digit Verification of cas no
The CAS Registry Mumber 90978-87-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,9,7 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90978-87:
(7*9)+(6*0)+(5*9)+(4*7)+(3*8)+(2*8)+(1*7)=183
183 % 10 = 3
So 90978-87-3 is a valid CAS Registry Number.
90978-87-3Relevant articles and documents
Synthesis and transformations of alkyl N-(1-cyclohex-3-enyl)carbamates prepared from cyclohex-3-ene carboxylic acid via Curtius rearrangement
Gómez-Sánchez, Elena,Marco-Contelles, José
, p. 1207 - 1219 (2007/10/03)
The Curtius rearrangement of cyclohex-3-ene carboxylic acid using diphenylphosphoryl azide in the presence of triethylamime and ethanol, t-butanol or benzyl alcohol has been described. As a result the synthesis of ethyl, t-butyl or benzyl N-(1-cyclohex-3-enyl)carbamates has been achieved in one pot, in good chemical yield. A series of transformations of benzyl N-(1-cyclohex-3-enyl)carbamate, such as iodination and epoxidation, as well as opening of the corresponding ring epoxide, have been carried out leading to some useful oxygenated cyclohexylamimo building blocks.
