103763-87-7 Usage
Uses
Used in Pharmaceutical Industry:
2-[2-Amino(methyl)anilino]-1-ethanol is used as a reactant for the preparation of substituted tetrahydroquinoxalines and tetrahydrobenzo[b][1,4]diazepines. These complex organic molecules have potential applications in the development of new pharmaceuticals, particularly in the treatment of various diseases and disorders.
Used in Chemical Synthesis:
In the field of chemical synthesis, 2-[2-Amino(methyl)anilino]-1-ethanol serves as a key intermediate in the production of various organic compounds. Its unique structure allows for the formation of multiple bonds and reactions, making it a valuable component in the synthesis of a wide range of molecules with diverse applications.
Used in Research and Development:
2-[2-Amino(methyl)anilino]-1-ethanol is also utilized in research and development for the exploration of new chemical reactions and the discovery of novel compounds. Its reactivity and structural versatility make it an ideal candidate for testing new synthetic methods and understanding the underlying mechanisms of various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 103763-87-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,7,6 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 103763-87:
(8*1)+(7*0)+(6*3)+(5*7)+(4*6)+(3*3)+(2*8)+(1*7)=117
117 % 10 = 7
So 103763-87-7 is a valid CAS Registry Number.
103763-87-7Relevant academic research and scientific papers
Preparation of substituted 1,2,3,4-tetrahydroquinoxalines and 2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepines from catalytic Cp*Ir hydrogen transfer N-heterocyclization of anilino alcohols
Todd Eary,Clausen, Dane
, p. 6899 - 6902 (2007/10/03)
The [Cp*IrCl2]2/K2CO3 catalyzed hydrogen transfer N-heterocyclization on a series of anilino alcohols has been investigated. The catalyst (20% loading) converts anilino alcohols to 1,2,3,4-tetrahydroquinoxalines and 2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepines in 30-84% isolated yield.
BENZOXADIAZOCINES, BENZOTHIADIAZOCINES AND BENZOTRIAZOCINES-IV; RING CLOSURE OF 1-PHENYL>-3-PHENYLTHIOUREAS. TETRAHYDROQUINOXALINE VS. DIHYDRO-3,1,6-BENZOTHIADIAZOCINE AND HEXAHYDRO-1,3,6-BENZOTRIAZOC
Hornyak, Gyula,Lempert, Karoly,Pjeczka, Etelka,Toth, Gabor
, p. 2847 - 2854 (2007/10/02)
While base induced ring closure of 1-phenyl>-3-phenylthioureas 1 had furnished the corresponding type 2 dihydro-3,1,6-benzothiadiazocine derivatives rather than the isomeric hexahydro-1,3,6-ben
