92022-10-1 Usage
Aromatic amine
A compound with a benzene ring and an amino group (-NH2) attached to the ring.
Bromo and chloro groups
Two halogen atoms (bromine and chlorine) attached to the benzene ring, which can influence the compound's reactivity and properties.
Alkoxy group
An ether functional group (-OR) attached to the carbon adjacent to the benzene ring, which can affect the compound's solubility and reactivity.
Building block and intermediate in organic synthesis
The compound can be used as a starting material or an intermediate in the synthesis of more complex organic compounds.
Application in medicinal chemistry
The compound is used in the synthesis of pharmaceutical compounds, potentially leading to new drugs and therapies.
Potential application in agrochemicals and materials science
The compound may have uses in the development of pesticides, herbicides, and other agricultural products, as well as in the creation of new materials with unique properties.
Hazards to human health and the environment
The compound may pose risks to human health and the environment due to its chemical properties and potential for exposure.
Safety measures
Appropriate precautions and safety measures should be taken when handling and using 2-(2-Bromobenzyloxy)-5-chloroaniline to minimize risks to human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 92022-10-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,0,2 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 92022-10:
(7*9)+(6*2)+(5*0)+(4*2)+(3*2)+(2*1)+(1*0)=91
91 % 10 = 1
So 92022-10-1 is a valid CAS Registry Number.
92022-10-1Relevant academic research and scientific papers
HECT E3 LIGASE INHIBITORS AND USES THEREOF
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Page/Page column 49-50, (2020/12/29)
The present invention relates to tricyclic derivatives of formula (I), which are useful as inhibitors of HECT-domain-containing E3 ligases, in particular NEDD4. The present invention also refers to pharmaceutical compositions comprising compounds of formu
Elaboration of the oxazepine ring system via cuI/L-proline-catalyzed intramolecular aryl amination
Guo, Lei,Li, Ben,Huang, Wenlong,Pei, Gang,Ma, Dawei
experimental part, p. 1833 - 1836 (2009/04/07)
A two-step approach for assembling oxazepines is described, which started from 2-aminophenols and substituted 2-bromobenzyl bromides and used CuI/L-proline-catalyzed coupling reaction as the key step. Georg Thieme Verlag Stuttgart.
