(S)-1-(4-Nitropheny...

(S)-1-(4-Nitrophenyl)ethylamine hydrochloride CAS NO.: 57233-86-0

(S)-1-(4-Nitrophenyl)ethylamine hydrochloride CAS NO.: 57233-86-0

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Keywords

(S)-1-(4-Nitrophenyl)ethylamine hydrochloride METHYL-4-NITROBENZYLAMINEHYDROCHLORIDE (R)-4-Nitro-α-methylbenzylamine hydrochloride

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  • Appearance:Colorless liquid
  • Application:Synthetic fragrances
  • PackAge:drum
  • ProductionCapacity:10000|Metric Ton|Month
  • Storage:Room temperature
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(S)-1-(4-Nitrophenyl)ethylamine hydrochloride Basic information
Product Name: (S)-1-(4-Nitrophenyl)ethylamine hydrochloride
Synonyms: METHYL-4-NITROBENZYLAMINEHYDROCHLORIDE;(R)-4-Nitro-α-methylbenzylamine hydrochloride;Benzenemethanamine, .alpha.-methyl-4-nitro-, monohydrochloride, (.alpha.R)-;(r)-α-methyl-4-nitrobenzylamine hydrochloride;(R)-A-METHYL-4-NITROBENZYLAMINE HYDROCHLORIDE,97%;(R)-(-)-1-(4-NITROPHENYL)-ETHYLAMINE HCL;(R)-1-(4-NITROPHENYL)ETHYLAMINE HYDROCHLORIDE;(R)-4-NITROPHENYL-1-ETHYLAMINE HYDROCHLORIDE
CAS: 57233-86-0
MF: C8H11ClN2O2
MW: 202.64
EINECS:  
Product Categories:  
Mol File: 57233-86-0.mol
(S)-1-(4-Nitrophenyl)ethylamine hydrochloride Structure
 
(S)-1-(4-Nitrophenyl)ethylamine hydrochloride Chemical Properties
Melting point  248-250 °C(lit.)
alpha  -6.5 º (c=1, 0.05N NaOH)
storage temp.  Inert atmosphere,Room Temperature
optical activity [α]25/D +6.0°, c = 1 in 0.05 M NaOH
BRN  3701567
CAS DataBase Reference 57233-86-0(CAS DataBase Reference)
 
Safety Information
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-37/39
WGK Germany  3
3-10
MSDS Information
Provider Language
SigmaAldrich English
 
(S)-1-(4-Nitrophenyl)ethylamine hydrochloride Usage And Synthesis
Purification Methods To ensure dryness, the hydrochloride (ca 175 g) is extracted with EtOH (3x100mL) and evaporated to dryness (any residual H2O increases the solubility in EtOH and lowers the yield). The hydrochloride residue is triturated with absolute EtOH and dried in vacuo. The product is further purified by refluxing with absolute EtOH (200 mL for 83g) for 1hour, and cool to 10o to give 76.6g of hydrochloride m 243-245o(dec). The free base is prepared by dissolving in N NaOH, extracting with CH2Cl2 (3 x 500mL), drying (Na2CO3), filtering, evaporating and distilling it. It has m 27o, b 119-120o/0.5mm (105-107o/0.5mm, 157-159o/9mm, d 1.1764, n 1.5688, [] ±17.7o (neat) [Perry et al. Synthesis 492 1977,ORD: Nerdel & Liebig Justus Liebigs Ann Chem 621 142 1959]. [Beilstein 12 IV 2451.]

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