149342-41-6 Usage
Chemical structure
N-(4-bromo-β-hydroxy-phenethyl)-acetamide is an organic compound with a phenethyl group attached to an acetamide via a beta-hydroxy and 4-bromo substituents.
Functional groups
The compound contains an amide group (-CONH2), a phenyl group (C6H5), a bromo substituent (Br), and a beta-hydroxy group (-OH).
Molecular weight
Approximately 214.07 g/mol
Appearance
The compound is likely to be a solid or crystalline substance, although the exact appearance may vary depending on the conditions.
Solubility
The solubility of N-(4-bromo-β-hydroxy-phenethyl)-acetamide is not explicitly mentioned, but it is likely to be soluble in organic solvents such as ethanol, methanol, or acetone due to its organic nature.
Synthesis
The compound is used in the synthesis of pharmaceuticals and biologically active molecules, indicating that it can be synthesized through various chemical reactions.
Applications
N-(4-bromo-β-hydroxy-phenethyl)-acetamide has potential applications in the development of new drugs and research into their effects on the human body, as well as in the field of medicinal chemistry and drug discovery.
Pharmacological activities
The presence of the bromo and hydroxy substituents may contribute to the compound's unique pharmacological activities, although specific activities are not mentioned in the provided material.
Safety and handling
As with any chemical compound, appropriate safety measures should be taken when handling N-(4-bromo-β-hydroxy-phenethyl)-acetamide, including the use of personal protective equipment and proper disposal methods.
Check Digit Verification of cas no
The CAS Registry Mumber 149342-41-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,3,4 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 149342-41:
(8*1)+(7*4)+(6*9)+(5*3)+(4*4)+(3*2)+(2*4)+(1*1)=136
136 % 10 = 6
So 149342-41-6 is a valid CAS Registry Number.
149342-41-6Relevant academic research and scientific papers
Baker's Yeast Reduction of α-(Acylamino)acetophenones and Lipase Catalyzed Resolution of 2-Acylamino-1-arylethanols
Izumi, Taeko,Fukaya, Katsumi
, p. 1216 - 1221 (2007/10/02)
Enzymatic reduction of α-acylaminoacetophenones with fermenting baker's yeast afforded optically active (R)-2-acylamino-1-arylethanols.Furthermore, lipase-catalyzed resolution of the 2-acylamino-1-arylethanols using vinyl acetate as an acyl donor resulted in the formation of (S)-1-acetoxy-2-acylamino-1-arylethanols and (R)-2-acylamino-1-arylethanols.
