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137542-74-6

(4R)-4-T-BUTYL-2-METHYL 2-OXAZOLINE is a chiral oxazoline derivative with the molecular formula C9H17NO. It possesses a specific three-dimensional arrangement of atoms, which makes it a valuable compound in chemical synthesis.
Used in Chemical Synthesis:
(4R)-4-T-BUTYL-2-METHYL 2-OXAZOLINE is used as a ligand in asymmetric catalysis for controlling the stereochemistry of chemical reactions. Its unique structure and properties make it useful in a variety of synthetic applications.
Used in Pharmaceutical Production:
(4R)-4-T-BUTYL-2-METHYL 2-OXAZOLINE is utilized in the production of pharmaceuticals and fine chemicals due to its ability to control stereochemistry, which is crucial for the development of effective and selective drugs.
Used in Biotechnology Research:
(4R)-4-T-BUTYL-2-METHYL 2-OXAZOLINE has been studied for its potential biological activities, although its specific effects are not yet fully understood. This suggests that it may have future applications in medicine and biotechnology once its properties are better characterized.

137542-74-6

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137542-74-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 137542-74-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,5,4 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 137542-74:
(8*1)+(7*3)+(6*7)+(5*5)+(4*4)+(3*2)+(2*7)+(1*4)=136
136 % 10 = 6
So 137542-74-6 is a valid CAS Registry Number.

137542-74-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-tert-butyl-2-methyl-4,5-dihydro-1,3-oxazole

1.2 Other means of identification

Product number -
Other names (4R)-4-T-BUTYL-2-METHYL 2-OXAZOLINE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:137542-74-6 SDS

137542-74-6Relevant articles and documents

Lewis acid-catalyzed asymmetric diels-alder reactions using chiral sulfoxide ligands: chiral 2-(arylsulfinylmethyl)-1,3-oxazoline derivatives.

Watanabe, Kazuhiro,Hirasawa, Takashi,Hiroi, Kunio

, p. 372 - 379 (2007/10/03)

New chiral sulfoxide-1,3-oxazoline ligands have been developed as chiral ligands for Lewis acid-catalyzed asymmetric Diels-Alder reactions. The use of chiral sulfinyl 1,3-oxazoline ligands in copper(II)-catalyzed asymmetric Diels-Alder reactions provided an endo cycloadduct as a major product with moderate enantioselectivity. A rationale is proposed for the mechanism of the asymmetric induction.

Asymmetric Michael Additions to α,β-Unsaturated Oxazolines. An Efficient Preparation of Chiral β,β-Disubstituted Propionaldehydes

Meyers, A. I.,Shipman, Michael

, p. 7098 - 7102 (2007/10/02)

A short stereoselective route to a variety of chiral, nonracemic α,β-unsaturated oxazolines derived from (S)-tert-leucinol is described.Addition of organolithium reagents to this chiral oxazoline occurs in a Michael fashion, giving rise to adducts with hi

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