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(S)-(−)-α-Methylbenzyl isocyanate

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For Research Use Only | Not For Clinical Use
CATAP14649037
CAS14649-03-7
Structure
MDL NumberMFCD00002036
Molecular Weight147.17
EC Number238-698-6
InChI KeyJJSCUXAFAJEQGB-QMMMGPOBSA-N
REAXYS Number4230972
Descriptionfor chiral derivatization, ≥99.0%
Density1.045 g/mL at 20 °C (lit.)
Assay≥99.0% (sum of enantiomers, GC); ≥99.0%
BP55-56 °C/2.5 mmHg (lit.)
Gradefor chiral derivatization
Linear FormulaC6H5CH(CH3)NCO
Refractive Indexn20/D 1.513; n20/D 1.5145 (lit.)
Size1ML, 5ML
Storage Conditions2-8°C
1

Absolute Configuration of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol Formed Metabolically From 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone

S S Hecht, T E Spratt, N Trushin

Carcinogenesis. 1997 Sep;18(9):1851-4.

PMID: 9328186

1

Determination of the Optical Purity of (R)-terbutaline by 1H-NMR and RP-LC Using Chiral Derivatizing Agent, (S)-(-)-alpha-methylbenzyl Isocyanate

K H Kim, H J Kim, J H Kim, J H Lee, S C Lee

J Pharm Biomed Anal. 2001 Jul;25(5-6):947-56.

PMID: 11377078

1

Enantiomeric Purity Test of Bevantolol by Reversed-Phase High Performance Liquid Chromatography After Derivatization With 2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyl Isothiocyanate

K H Kim, S Y Heo, S P Hong, B C Lee

Arch Pharm Res. 2000 Dec;23(6):568-73.

PMID: 11156176

1

Quantitation of 4-oxo-4-(3-pyridyl)butanoic Acid and Enantiomers of 4-hydroxy-4-(3-pyridyl)butanoic Acid in Human Urine: A Substantial Pathway of Nicotine Metabolism

S S Hecht, D K Hatsukami, L E Bonilla, J B Hochalter

Chem Res Toxicol. 1999 Feb;12(2):172-9.

PMID: 10027795

1

Resolution of Salbutamol Enantiomers in Human Urine by Reversed-Phase High Performance Liquid Chromatography After Derivatization With (S)-(-)-alpha-methylbenzyl Isocyanate

K H Kim, T K Kim, Y H Kwon, Y T Sohn

Arch Pharm Res. 1997 Oct;20(5):486-90.

PMID: 18982495

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