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3-Isoxazolecarboxylic acid, 5-(phenylacetyl)-4-(2,5,5-trimethyl-1,3-dioxan-2-yl)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

646066-63-9

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646066-63-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 646066-63-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,6,0,6 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 646066-63:
(8*6)+(7*4)+(6*6)+(5*0)+(4*6)+(3*6)+(2*6)+(1*3)=169
169 % 10 = 9
So 646066-63-9 is a valid CAS Registry Number.

646066-63-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(2-phenyl-1-keto-ethyl)-4-(2,5,5-trimethyl-1,3-dioxan-2-yl) 3-isoxazolecarboxylic acid ethyl ester

1.2 Other means of identification

Product number -
Other names 5-(2-phenyl-1-keto-ethyl)-4-(2,5,5-trimethyl-1,3-dioxan-2-yl)-3-isoxazolecarboxylic acid ethyl ester

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:646066-63-9 SDS

646066-63-9Relevant academic research and scientific papers

Preparation of Keto-Isoxazole Polyketide Synthons

Nelson, Jared K.,Burkhart, David J.,McKenzie, Andrew,Natale, Nicholas R.

, p. 2213 - 2215 (2003)

The Dess-Martin periodinane (DMP) oxidation of alcohols, proceeds in good to excellent yield in the presence of the isoxazole ring, and other nitrogen-containing functional groups. The DMP route allows for the preparation of highly branched polyketide syn

Preparation of chiral isoxazole carbinols via catalytic asymmetric Corey-Bakshi-Shibata reduction

Rider, Kevin C.,Burkhart, David J.,Li, Chun,Mckenzie, Andrew R.,Nelson, Jared K.,Natale, Nicholas R.

experimental part, p. 97 - 107 (2010/09/04)

A diverse set of isoxazoles, with activity in three different disease categories, was reduced asymmetrically from pro-chiral ketones to chiral alcohols using the Corey-Bakshi-Shibata methodology at the α, β, and γ positions relative to the C-5-methyl of the isoxazole. The experiments described provide an easy route to hydroxylated isoxazoles that represent the common CYP-450 3A4 metabolic site.

Catalytic asymmetric synthesis of glutamate analogues

Burkhart, David J.,McKenzie, Andrew R.,Nelson, Jared K.,Myers, Katherine I.,Zhao, Xue,Magnusson, Kathy R.,Natale, Nicholas R.

, p. 1285 - 1288 (2007/10/03)

Utilizing our lateral metalation coupled with Jacobsen's catalytic asymmetric amino nitrile synthesis, we have demonstrated the ability to synthesize isoxazole-containing amino acid glutamate analogues in high yield and high enantiomeric excesses. Chiral

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