404-70-6 Usage
Description
3-Fluorophenethylamine is an organic compound that features a fluorine atom attached to a phenyl ring and an ethylamine group. It is known for its potential applications in the synthesis of various chemical compounds and pharmaceuticals.
Uses
Used in Pharmaceutical Industry:
3-Fluorophenethylamine is used as a synthetic intermediate for the development of various pharmaceutical compounds. Its unique structure allows it to be a key component in the creation of new drugs with potential therapeutic properties.
Used in the Synthesis of N-(3-Fluorophenyl)Ethylcaffeamide:
3-Fluorophenethylamine is used as a building block in the synthesis of N-(3-Fluorophenyl)Ethylcaffeamide, a compound that has been evaluated for its anti-inflammatory activity. Its presence in this compound may contribute to its potential therapeutic effects.
Used in the Synthesis of N-2-[(3-Fluorophenyl)Ethyl]-2-Methylpropanamide:
3-Fluorophenethylamine is also used in the synthesis of N-2-[(3-Fluorophenyl)Ethyl]-2-Methylpropanamide, another compound that may have potential applications in various fields, such as medicine or chemical research.
Used in the Synthesis of N-(3′-Fluorophenyl)Ethyl-4-Azahexacyclo[5.4.1.02,6.03,10.05,9.08,11]dodecan-3-ol:
3-Fluorophenethylamine is utilized in the synthesis of N-(3′-Fluorophenyl)Ethyl-4-Azahexacyclo[5.4.1.02,6.03,10.05,9.08,11]dodecan-3-ol, a complex molecule that may have unique properties and potential uses in various industries, including pharmaceuticals and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 404-70-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,0 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 404-70:
(5*4)+(4*0)+(3*4)+(2*7)+(1*0)=46
46 % 10 = 6
So 404-70-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H10FN/c9-8-3-1-2-7(6-8)4-5-10/h1-3,6H,4-5,10H2/p+1
404-70-6Relevant articles and documents
Bi-enzymatic Conversion of Cinnamic Acids to 2-Arylethylamines
Weise, Nicholas J.,Thapa, Prasansa,Ahmed, Syed T.,Heath, Rachel S.,Parmeggiani, Fabio,Turner, Nicholas J.,Flitsch, Sabine L.
, p. 995 - 998 (2020/01/21)
The conversion of carboxylic acids, such as acrylic acids, to amines is a transformation that remains challenging in synthetic organic chemistry. Despite the ubiquity of similar moieties in natural metabolic pathways, biocatalytic routes seem to have been overlooked for this purpose. Herein we present the conception and optimisation of a two-enzyme system, allowing the synthesis of β-phenylethylamine derivatives from readily-available ring-substituted cinnamic acids. After characterisation of both parts of the reaction in a two-step approach, a set of conditions allowing the one-pot biotransformation was optimised. This combination of a reversible deaminating and irreversible decarboxylating enzyme, both specific for the amino acid intermediate in tandem, represents a general method by which new strategies for the conversion of carboxylic acids to amines could be designed.
DOLASTATIN-10 DERIVATIVE, METHOD OF PRODUCING SAME AND ANTICANCER DRUG COMPOSITION CONTAINING SAME
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Paragraph 0089; 0090; 0091; 0092; 0093; 0094, (2015/07/15)
The present invention provides a dolastatin-10 derivative having excellent anticancer activity, a method of producing the same and anticancer drug composition containing the same as an active ingredient.
PRODUCTION OF INDUCED PLURIPOTENT STEM CELLS
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, (2012/06/30)
The present disclosure relates to methods and compositions that improve the in vitro production of induced pluripotent stem cells through the use of compounds that promote degradation of p53. The disclosure also relates to compositions and methods for the treatment of cancer, pancreatitis and intracellular pathogens.
