912284-73-2 Usage
Molecular structure
2-(2-Amino-4-dimethylanilino)-1-ethanol consists of an amino group, dimethylamino group, and an ethanol functional group.
Usage
It is commonly used as an intermediate in the synthesis of various pharmaceuticals and organic compounds.
Chemical properties
Due to its structural features, this compound has the potential to exhibit both basic and nucleophilic properties, making it useful in organic synthesis and medicinal chemistry.
Applications
It may also have applications in the development of dyes, pigments, and other fine chemicals.
Safety precautions
Proper handling and safety precautions should be observed when working with 2-(2-Amino-4-dimethylanilino)-1-ethanol.
Check Digit Verification of cas no
The CAS Registry Mumber 912284-73-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,2,2,8 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 912284-73:
(8*9)+(7*1)+(6*2)+(5*2)+(4*8)+(3*4)+(2*7)+(1*3)=162
162 % 10 = 2
So 912284-73-2 is a valid CAS Registry Number.
912284-73-2Relevant articles and documents
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.
