37844-06-7 Usage
Uses
Due to the limited information available on the hazards or potential applications of b-Amino-3-chlorobenzenepropanol, its uses are not well-documented. However, given its chemical structure, it is likely that b-AMino-3-chlorobenzenepropanol could be used in the synthesis of other chemical compounds, particularly those that require a benzene ring and functional groups such as amino and chloro.
Used in Chemical Synthesis:
b-Amino-3-chlorobenzenepropanol is used as a building block for the synthesis of other chemical compounds, leveraging its benzene ring and functional groups for various reactions and applications. The presence of the amino and chloro groups may allow for further chemical modifications, making it a versatile intermediate in organic chemistry.
Used in Pharmaceutical Research:
Although not widely studied, b-Amino-3-chlorobenzenepropanol may have potential applications in pharmaceutical research. Its chemical structure could be explored for the development of new drugs, particularly if its reactivity and functional groups can be harnessed to create bioactive molecules.
Used in Material Science:
b-AMino-3-chlorobenzenepropanol's structure may also be of interest in material science, where its properties could be investigated for potential use in the development of new materials with specific characteristics, such as improved stability or reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 37844-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,8,4 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 37844-06:
(7*3)+(6*7)+(5*8)+(4*4)+(3*4)+(2*0)+(1*6)=137
137 % 10 = 7
So 37844-06-7 is a valid CAS Registry Number.
37844-06-7Relevant academic research and scientific papers
Nucleophilic RhI Catalyzed Selective Isomerization of Terminal Aziridines to Enamides
Tian, Yingying,Kunz, Doris
, p. 4272 - 4275 (2020/07/04)
The selective isomerization of various terminal N-Boc protected aziridines to enamides was realized using the highly reactive nucleophilic rhodium catalyst C with the Lewis acid LiNTf2 as co-catalyst under moderate conditions. The reaction proceeds smoothly with only 1 molpercent catalyst loading and excellent yields were achieved. An intermediate containing an enamide with a non-conjugated terminal C=C double bond was detected during the course of the reaction, which isomerizes to form the thermodynamically favored 2-amido styrene. Mechanistic insight is gained based on these observations.
