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(S)-(−)-α-Methylbenzylamine

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For Research Use Only | Not For Clinical Use
CATAP2627863
CAS2627-86-3
Structure
MDL NumberMFCD00064406
Molecular Weight121.18
EC Number220-098-0
InChI KeyRQEUFEKYXDPUSK-ZETCQYMHSA-N
REAXYS Number2204907
Descriptionfor chiral derivatization, ≥99.0%
Density0.94 g/mL at 25 °C (lit.)
Assay≥99.0% (sum of enantiomers, GC); ≥99.0%
BP187 °C (lit.)
Gradefor chiral derivatization
Linear FormulaC6H5CH(CH3)NH2
Refractive Indexn20/D 1.526 (lit.); n20/D 1.528
Size5ML, 25ML
Storage Conditions2-8°C
Vapor Pressure0.5 mmHg ( 20 °C)
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1

Asymmetric Synthesis of (S)-alpha-methylbenzylamine by Recombinant Escherichia Coli Co-Expressing Omega-Transaminase and Acetolactate Synthase

Hyungdon Yun, Byung-Gee Kim

Biosci Biotechnol Biochem. 2008 Nov;72(11):3030-3.

PMID: 18997410

Read More
1

Looking Inside the Intramolecular C-H∙∙∙O Hydrogen Bond in Lactams Derived From α-Methylbenzylamine

Sandra Mejía, Julio M Hernández-Pérez, Jacinto Sandoval-Lira, Fernando Sartillo-Piscil

Molecules. 2017 Feb 28;22(3):361.

PMID: 28264508

Read More
1

Necessary and Sufficient Conditions for the Asymmetric Synthesis of Chiral Amines Using ω-aminotransferases

Joo-Hyun Seo, Dohyun Kyung, Keehyoung Joo, Jooyoung Lee, Byung-Gee Kim

Biotechnol Bioeng. 2011 Feb;108(2):253-63.

PMID: 20824676

Read More
1

Solvent Effects on the Optical Rotation of (S)-(-)-alpha-methylbenzylamine

Andrew T Fischer, Robert N Compton, Richard M Pagni

J Phys Chem A. 2006 Jun 8;110(22):7067-71.

PMID: 16737254

Read More
1

Tailoring D-amino Acid Oxidase From the Pig Kidney to R-stereoselective Amine Oxidase and Its Use in the Deracemization of α-methylbenzylamine

Kazuyuki Yasukawa, Shogo Nakano, Yasuhisa Asano

Angew Chem Int Ed Engl. 2014 Apr 22;53(17):4428-31.

PMID: 24644036

Read More
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