14467-32-4

Basic information

• Product Name: (S)-(+)-2-TERT-BUTYLAMINO-1-PHENYLETHAN&
• Synonyms: (S)-(+)-2-TERT-BUTYLAMINO-1-PHENYLETHAN&
• CAS NO: 14467-32-4
• Molecular Formula: C₁₂H₁₉NO
• Molecular Weight: 193.29
• Product Categories: Amino Alcohols;Chiral Building Blocks;Organic Building Blocks
• Mol File: 14467-32-4.mol
• Article Data: 29

Chemical Properties

• Melting Point: 105-108 °C(lit.)
• Boiling Point: 284°Cat760mmHg
• Flash Point: 80.7°C
• Appearance: /
• Density: 0.989g/cm³
• Vapor Pressure: 0.001mmHg at 25°C
• Refractive Index: 1.52
• CAS DataBase Reference: (S)-(+)-2-TERT-BUTYLAMINO-1-PHENYLETHAN&(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-(+)-2-TERT-BUTYLAMINO-1-PHENYLETHAN&(14467-32-4)
• EPA Substance Registry System: (S)-(+)-2-TERT-BUTYLAMINO-1-PHENYLETHAN&(14467-32-4)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 14467-32-4(Hazardous Substances Data)

Usage

General Description

(S)-(+)-2-tert-butylamino-1-phenylethan is a chemical compound with a molecular formula of C12H19N. It is a chiral compound with a molecular weight of 181.28 g/mol. (S)-(+)-2-TERT-BUTYLAMINO-1-PHENYLETHAN& is commonly used as a reactant in the synthesis of other organic compounds and pharmaceuticals. Its stereochemistry makes it useful for creating enantiomerically pure products, which is important in drug development and other applications where chirality is crucial. (S)-(+)-2-TERT-BUTYLAMINO-1-PHENYLETHAN& is also used as a building block in the synthesis of various biologically active molecules.

InChI:InChI=1/C12H19NO/c1-12(2,3)13-9-11(14)10-7-5-4-6-8-10/h4-8,11,13-14H,9H2,1-3H3/t11-/m1/s1

Upstream product

• 100-42-5 styrene 
• 50381-48-1 trioxo(N-tert-butylimido)osmium(VIII) 
• 63174-13-0 bis(tert-butylimino)dioxoosmium 
• 96-09-3 styrene oxide 
• 75-64-9 tert-butylamine 
• 5577-67-3 trimethyl(tert-butylamino)silane 
• 469874-36-0 S(+)-N-tert-butyl-O-acetyl mandelamid 
• 70111-05-6 (S)-2-chloro-1-phenylethanol 
• 119072-55-8 tert-butylisonitrile 
• 100-52-7 benzaldehyde 
• 91850-96-3 2-(tert-butylimino)-1-phenylethanone 
• 7322-88-5 (S)-acetylmandelic acid 
• 17199-29-0 (S)-Mandelic acid 
• 79866-39-0 2-(tert-butylamino)-1-phenylethanone hydrochloride 

Downstream Products

• 18366-49-9 1-tert-butyl-2-phenylaziridine 
• 18366-84-2 3-tert-butyl-5r-phenyl-[1,2,3]oxathiazolidine 2t-oxide 
• 18366-84-2 3-tert-butyl-5r-phenyl-[1,2,3]oxathiazolidine 2c-oxide 

Relevant articles and documents

Asymmetric Reduction of α-Ketoimines with Oxazaborolidine Catalysts: A Novel, Practical Approach to Chiral Arylethanolamines

Asymmetric borane reduction of α-ketoimines with oxazaborolidine catalysts has been studied.The ee's of the resulting arylethanolamines are uo to 93percent using 20 molpercent of the catalyst.

Efficient Synthesis of 2-Amino-1-Arylethanols Through a Lewis Base-Catalyzed SiCl4-Mediated Asymmetric Passerini-Type Reaction

We herein report, a practical and efficient strategy for the synthesis of enantiomerically enriched 2-amino-1-arylethanols, a structural motif commonly encountered in the family of β-adrenergic blockers or agonists, through a Lewis base-catalyzed SiClsub

Method for Ir/f-amphox high-efficiency synthesis of chiral α- C-amino alcohol by virtue of catalytic oxidation 1,2- of P-aminoketone by using one-aminoketone

The invention discloses a method for efficiently synthesizing chiral 1,2-amino alcohol by catalyzing alpha-aminoketone through Ir/f-amphox. A ligand f-amphox used by the method can be more easily synthesized; the reaction has the characteristics of enanti