(S)-ALPHA-METHYL-4-NITROBENZYLAMINE HYDROCHLORIDE
(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
(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)
MSDS
- Language:English Provider:SigmaAldrich
(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
- Tel
- 010-82848833 400-666-7788
- jkinfo@jkchemical.com
- Tel
- 021-61259108 18621169109
- market03@meryer.com
- Tel
- +86-21-20908456
- sales@BioChemBest.com
- Tel
- 021-67121386
- Sales-CN@TCIchemicals.com
- Tel
- 021-021-58432009 400-005-6266
- sales8178@energy-chemical.com
(S)-ALPHA-METHYL-4-NITROBENZYLAMINE HYDROCHLORIDE(132873-57-5)Related Product Information
- Ammonium sulfate
- Ethylamine hydrochloride
- (R)-ALPHA-METHYL-4-NITROBENZYLAMINE HYDROCHLORIDE
- S-(-)-a-Methyl-p-aminobenzylamine
- (S)-1-(4-NITROPHENYL)-ETHYLAMINE
- 4-Nitrobenzylamine hydrochloride
- ALFA-ALFA-DIMETHYL-P-NITRO-BENZYLAMINE HYDROCHLORIDE
- 4-(1-AMINO-ETHYL)-PHENYLAMINE
- (S)-ALPHA-METHYL-4-NITROBENZYLAMINE HYDROCHLORIDE
- (1R,2R)-(+)-1,2-Bis(4-nitrophenyl)ethylenediaminedihydrochloride,min.98%