92259-19-3 Usage
Uses
Used in Organic Synthesis:
1-(3-nitrophenyl)ethanaMine hydrochloride is used as a versatile intermediate for the synthesis of various organic compounds. Its nitrophenyl group allows it to participate in a range of chemical reactions, making it a valuable component in the creation of new molecules with potential applications across different industries.
Used in Research Settings:
In research, 1-(3-nitrophenyl)ethanaMine hydrochloride is used as a reagent in chemical reactions. Its solubility in water and crystalline nature make it an ideal candidate for experimental procedures, facilitating the study of chemical properties and reactions involving amines and their derivatives.
Used in Pharmaceutical Industry:
1-(3-nitrophenyl)ethanaMine hydrochloride is used as a building block in the development of pharmaceutical compounds. Its ability to undergo various chemical transformations positions it as a key component in the synthesis of new drugs, potentially contributing to the discovery of novel therapeutic agents.
Used in Chemical Reactions as a Reagent:
In the chemical industry, 1-(3-nitrophenyl)ethanaMine hydrochloride is utilized as a reagent to catalyze or facilitate specific reactions. Its properties enable it to interact with other molecules, driving reactions forward and aiding in the production of desired chemical products.
Each application underscores the compound's importance in the realms of chemistry and research, highlighting its potential to contribute to advancements in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 92259-19-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,2,5 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 92259-19:
(7*9)+(6*2)+(5*2)+(4*5)+(3*9)+(2*1)+(1*9)=143
143 % 10 = 3
So 92259-19-3 is a valid CAS Registry Number.
92259-19-3Relevant academic research and scientific papers
Enantiomerically enriched 1-phenylethylamines
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Page/Page column 8, (2010/02/10)
Production of enantiomerically enriched 1-(mono-, di- or trinitro-phenyl)-ethylamine derivatives (I) comprises reacting a nitro-acetophenone derivative (III) with a hydroxylamine compound (IV), reducing the obtained oxime compound (V) using a complex borohydride and an acid in organic solvent to give (I) in racemic form and enantiomerically enriching using an enantiomerically enriched acid. Production of enantiomerically enriched 1-(mono-, di- or trinitro-phenyl)-ethylamine derivatives of formula (I) comprises: (1) reacting an acetophenone derivative of formula (III) with a hydroxylamine compound of formula R5>ONH2.aHX (IV) to give an oxime of formula (V); (2) reducing (V) using a complex borohydride and an acid in organic solvent to give (I) in racemic form, and (3) enantiomerically enriching the product using an enantiomerically enriched acid. [Image] n : 1-3; m : 0 to (5-n); R1>1-12C alkyl, 1-12C alkoxy, 1-12C alkylthio, 5-14C aryl, 5-14C aryloxy, 6-15C aralkyl, 6-15C aralkoxy, F, Cl, CN, optionally protected CHO, optionally protected OH, optionally protected SH, 1-12C haloalkyl, 1-12C haloalkoxy, 1-12C haloalkylthio, A-B'-C(O)-E or A-E; A : a direct bond, 1-8C alkylene, 1-8C alkenylene or 1-8C haloalkylene; B' : a direct bond, O, S or NR2>; R2>H, 1-8C alkyl, 6-15C aralkyl or 5-14C aryl; E : OR3> or N(R4>)2; R3>1-8C alkyl, 6-15C aralkyl or 5-14C aryl; R4>H, 1-8C alkyl, 6-15C aralkyl or 5-14C aryl, or N(R4>)24-12C cyclic amino; a : 0 or 1; R5>H or 1-12C alkyl, and X : anion. Independent claims are included for new diastereomerically enriched salts of (I) having formula (I).HRx> (I') and new enantiomerically enriched salts of (I) having formula (I).HX' (I''). Rx>anion of an enantiomerically enriched organic acid, and X' : halide.
