ChemicalBook Product Catalog Organic Chemistry Amides Acyclic polyamines and their derivatives 4-Nitrophenethylamine hydrochloride

4-Nitrophenethylamine hydrochloride

4-Nitrophenethylamine hydrochloride Basic information
Product Name:4-Nitrophenethylamine hydrochloride
Synonyms:4-NitrophenylethylaMineydrochloride SynonyMs 2-(4-Nitrophenyl)ethylaMine hydrochloride;4- nitrobenzeneethylaMine hydrochloride;4-NitrophenylethylaMine HCl ( SM of Mirabegron );P-nitrophenyl riMantadine hydrochloride;4-NitrophenylethylaMinehydrochloride SynonyMs 2-(4-Nitrophenyl)ethylaMine hydrochloride;β-(p-Nitrophenyl)ethylamine hydrochloride;4-Nitrophenethylamine hydrochloride 95%;4-NITROPHENYLETHYLAMINE HCL
CAS:29968-78-3
MF:C8H11ClN2O2
MW:202.64
EINECS:249-980-3
Product Categories:Nitro / Nitriles;Anilines, Aromatic Amines and Nitro Compounds;Benzene derivatives;pharmacetical;API intermediates;1;29968-78-3
Mol File:29968-78-3.mol
4-Nitrophenethylamine hydrochloride Structure
4-Nitrophenethylamine hydrochloride Chemical Properties
Melting point 200 °C (dec.)(lit.)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Soluble in methanol almost transparency.
form Crystalline Powder
color Yellow to yellow-green
BRN 3568915
Stability:Hygroscopic
InChIKeyJVMHULJEYUQYSH-UHFFFAOYSA-N
CAS DataBase Reference29968-78-3(CAS DataBase Reference)
Safety Information
Hazard Codes Xn
Risk Statements 36/37/38-40
Safety Statements 22-24/25-36-26
WGK Germany 3
HS Code 29214990
MSDS Information
ProviderLanguage
2-(4-Nitrophenyl)ethylamine hydrochloride English
SigmaAldrich English
ACROS English
4-Nitrophenethylamine hydrochloride Usage And Synthesis
Chemical Propertiesyellow to brown crystalline powder and chunks
Uses4-Nitrophenethylamine hydrochloride was used in the synthesis of ortho-metalated primary phenethylamines complexes containing six-membered palladacycles and N-(4-nitrophenethyl)formamide.
PreparationThe preparation of 4-Nitrophenethylamine hydrochloride is as follows:Ten mL of 2M HCl was then added in a one-pot fashion, and, in all cases but threonine, the reaction vessel was heated to 190°Cover 5 min with stirring and then allowed to cool. In the case of the temperature-sensitive threonine, soxhlet extraction with toluene was performed at 80°C to remove R-carvone from the reaction mixture. The aqueous reaction mixture was washed three times with 25 mL of ether, and then water solvent was distilled off from the hydrochloride salt. The hydrochloride salt was transferred to a vacuum oven and dried overnight at 150 °C and 10 Torr.

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2-AMINO-1-(4-NITROPHENYL)ETHAN-1-ONE HYDROCHLORIDE HYDRATE Chloramphenicol sodium succinate CHLORAMPHENICOL CINNAMATE Triethylamine hydrochloride 1-(2-CHLOROANILINO)-3-(4-NITROPHENYL)-3-OXO-2-PYRIDINIUM-1-YLPROP-1-ENE-1-THIOLATE LABOTEST-BB LT00441005 2-Chloroethylamine hydrochloride Topotecan hydrochloride Chloramphenicol p-Nitrobenzoic acid 4-Nitrophenethylamine hydrochloride Ethylamine hydrochloride 2-Phenylethylamine hydrochloride Nitrobenzene L-4-Nitrophenylalanine methyl ester hydrochloride Ethylamine Nitrophenyl 1,3-Dinitrobenzene
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