Basic information Safety Supplier Related

(S)-ALPHA-METHYL-4-NITROBENZYLAMINE HYDROCHLORIDE

Basic information Safety Supplier Related

(S)-ALPHA-METHYL-4-NITROBENZYLAMINE HYDROCHLORIDE Basic information

Product Name:
(S)-ALPHA-METHYL-4-NITROBENZYLAMINE HYDROCHLORIDE
Synonyms:
  • (S)-(+)-1-(4-NITROPHENYL)-ETHYLAMINE HCL
  • (S)-1-(4-NITROPHENYL)-METHYLAMIN HYDROCHLORIDE
  • (S)-4-NITROPHENYL-1-ETHYLAMINE HYDROCHLORIDE
  • (S)-NITRESOLVE
  • (S)-(+)-ALPHA-METHYL-4-NITROBENZYLAMINE HCL
  • (S)-ALPHA-METHYL-4-NITROBENZYLAMINE HYDROCHLORIDE
  • (S)-ALPHA-METHYL-4-NITROBENZYLAMMONIUM CHLORIDE
  • (S)-(+)-ALPHA-METHYL-P-NITROBENZYLAMINE HYDROCHLORIDE
CAS:
132873-57-5
MF:
C8H11ClN2O2
MW:
202.64
Product Categories:
  • chiral
  • for Resolution of Acids
  • Optical Resolution
  • Synthetic Organic Chemistry
  • 1
Mol File:
132873-57-5.mol
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(S)-ALPHA-METHYL-4-NITROBENZYLAMINE HYDROCHLORIDE Chemical Properties

Melting point:
248-250 °C(lit.)
refractive index 
-7.2 ° (C=1, 0.05mol/L NaOH)
storage temp. 
Inert atmosphere,Room Temperature
form 
powder to crystal
color 
White to Light yellow
optical activity
[α]25/D 6.5°, c = 1 in 0.05 M NaOH
Water Solubility 
faint turbidity
CAS DataBase Reference
132873-57-5(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39
WGK Germany 
3
3-10
HS Code 
29214990

MSDS

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(S)-ALPHA-METHYL-4-NITROBENZYLAMINE HYDROCHLORIDE Usage And Synthesis

Uses

(S)-α-Methyl-4-nitrobenzylamine hydrochloride can be used as:

  • A fluorescence-quenching guest in the determination of chiral recognition capabilities of binaphthocrown ether and polythiophene complex.
  • A starting material in the synthesis of chiral cyclopalladated complexes with applications in the resolution of racemic compounds.

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.]

(S)-ALPHA-METHYL-4-NITROBENZYLAMINE HYDROCHLORIDESupplier

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