13534-87-7 Usage
Derivation
It is derived from acetylphenylamine and ethyl acetate.
Usage
Commonly used in the production of pharmaceuticals and organic synthesis.
Physical appearance
White to pale yellow solid.
Odor
Strong aromatic odor.
Solubility
Soluble in alcohol, ether, and chloroform.
Primary use
Utilized as an intermediate in the manufacturing of various pharmaceuticals, dyes, and other organic compounds.
Hazards
Possesses potential hazards and should be handled with care.
Safety precautions
Follow proper safety protocols and guidelines when handling the chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 13534-87-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,3 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13534-87:
(7*1)+(6*3)+(5*5)+(4*3)+(3*4)+(2*8)+(1*7)=97
97 % 10 = 7
So 13534-87-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H15NO3/c1-10(14)13(8-9-16-11(2)15)12-6-4-3-5-7-12/h3-7H,8-9H2,1-2H3
13534-87-7Relevant articles and documents
Synthesis of indole, benzofuran and benzothiophene by pyrolysis of 2-anilinoethanol, 2-phenoxyethanol and 2-(phenylthio)ethanol acetates
Afxantidis, Jean,Aune, Jean-Pierre
, p. 395 - 403 (2007/10/03)
The synthesis of indole is possible by pyrolysis of compounds of the general formula : ΦNHCH2CH2X. The pyrolysis of the acetates (X = OCOCH3) of 2-anilinoethanol 3a, 2-phenoxyethanol 3b and 2-(phenylthio)ethanol 3c was studied by surface response methodology. A possible mechanism involving a radical pathway is discussed in terms of bond dissociation energies, thermal stability of the pyrolysis products and configuration of the radical intermediates. Elsevier,.
