24687-79-4 Usage
General Description
The chemical 2-[(3,4-dimethoxybenzyl)amino]ethanol is a compound with a molecular formula C11H17NO3. It is an amino alcohol with a benzyl group that contains two methoxy (CH3O-) substituents. 2-[(3,4-dimethoxybenzyl)amino]ethanol has potential applications in the pharmaceutical industry, particularly as a building block for the synthesis of various drugs. It may also have uses in research and development, as well as in the production of specialty chemicals. The specific properties and potential uses of 2-[(3,4-dimethoxybenzyl)amino]ethanol may vary depending on the exact application and context in which it is used.
Check Digit Verification of cas no
The CAS Registry Mumber 24687-79-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,6,8 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24687-79:
(7*2)+(6*4)+(5*6)+(4*8)+(3*7)+(2*7)+(1*9)=144
144 % 10 = 4
So 24687-79-4 is a valid CAS Registry Number.
24687-79-4Relevant articles and documents
An Alternative Approach to the Hydrated Imidazoline Ring Expansion (HIRE) of Diarene-Fused [1.4]Oxazepines
Grintsevich, Sergey,Sapegin, Alexander,Reutskaya, Elena,Peintner, Stefan,Erdélyi, Máté,Krasavin, Mikhail
, p. 5664 - 5676 (2020/07/21)
A four-step approach to the “hydrated imidazoline ring expansion” (HIRE) is presented. In most cases, the ring expansion was the sole process. However, for the first time, an alternative course of the hydrated imidazoline evolution was discovered which gave N-aminoethyl derivatives. These can, in principle, be converted into the target HIRE products under sufficiently forcing conditions. The approach offers improved flexibility with respect to the peripheral substituents and is also applicable to the synthesis of eleven-membered lactams. We observed that the latter can exist in two stable isomeric forms due to lactam–amide bond isomerization. The latter finding further demonstrates the value of medium-sized rings as multiple-conformer probes for biological target interrogation.
