(S)-(-)-α-Methyl-4-Nitrobenzylamine Hydrochloride CAS 132873-57-5 Purity >99.0% (HPLC) Factory

(S)-(-)-α-Methyl-4-Nitrobenzylamine Hydrochloride (S)-1-(4-Nitrophenyl)ethylamine Hydrochloride CAS: 132873-57-5 Purity: >99.0% (HPLC)   Appearance: Off-White or Yellowish Powder High Quality, Commercial Production E-Mail: alvin@ruifuchem.com

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Package: Bottle, Aluminium foil bag, 25kg/Cardboard Drum, or according to customer's requirement Storage Condition: Store in sealed containers at cool and dry place; Protect from light and moistureShanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of (S)-(-)-α-Methyl-4-Nitrobenzylamine Hydrochloride (CAS: 132873-57-5) with high quality, commercial production. We can provide Certificate of Analysis (COA), worldwide delivery, small and bulk quantities available, strong after-sale service. Please contact: alvin@ruifuchem.com
Item Specifications
Appearance Off-White or Yellowish Powder
Purity / Analysis Method >99.0% (HPLC)
Melting Point 240.0~250.0℃
Specific Rotation -6.0±2.0° (C=1, 0.05N NaOH)
Water (K.F) <0.50%
Single Impurity <0.50%
Total Impurities <1.00%
Test Standard Enterprise Standard
Usage Pharmaceutical Intermediates

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Chemical Name (S)-(-)-α-Methyl-4-Nitrobenzylamine Hydrochloride
Synonyms (S)-α-Methyl-4-Nitrobenzylamine Hydrochloride; (S)-1-(4-Nitrophenyl)ethylamine Hydrochloride; (S)-alpha-Methyl-4-Nitrobenzylamine Hydrochloride
CAS Number 132873-57-5
CAT Number RF-CC335
Stock Status In Stock, Production Scale Up to Tons
Molecular Formula C8H11ClN2O2
Molecular Weight 202.64
Brand Ruifu Chemical

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Application:

(S)-(-)-α-Methyl-4-Nitrobenzylamine Hydrochloride (CAS: 132873-57-5) 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. (S)-(-)-α-Methyl-4-Nitrobenzylamine Hydrochloride is a useful research chemical used in the preparation of peptoids as inhibitors of HDM2-p53 interactions.

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