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Oxazole, 5-methoxy-2-phenyl-4-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64686-60-8

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64686-60-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64686-60-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,6,8 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 64686-60:
(7*6)+(6*4)+(5*6)+(4*8)+(3*6)+(2*6)+(1*0)=158
158 % 10 = 8
So 64686-60-8 is a valid CAS Registry Number.

64686-60-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-benzyl-2-phenyl-5-methoxyoxazole

1.2 Other means of identification

Product number -
Other names 4-benzyl-5-methoxy-2-phenyl-oxazole

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:64686-60-8 SDS

64686-60-8Downstream Products

64686-60-8Relevant academic research and scientific papers

Triflic anhydride-mediated synthesis of oxazoles

Thalhammer, Armin,Mecinovi?, Jasmin,Schofield, Christopher J.

supporting information; experimental part, p. 1045 - 1047 (2009/05/31)

N-Acyl amino acid esters undergo triflic anhydride-mediated cyclodehydration to form oxazoles and bisoxazoles in a simple one-pot transformation.

A versatile cyclodehydration reaction for the synthesis of isoquinoline and β-carboline derivatives

Movassaghi, Mohammad,Hill, Matthew D.

supporting information; experimental part, p. 3485 - 3488 (2009/05/07)

(Chemical Equation Presented) The direct conversion of various amides to isoquinoline and β-carboline derivatives via mild electrophilic amide activation, with trifluoromethanesulfonic anhydride in the presence of 2-chloropyridine, is described. Low-temperature amide activation followed by cyclodehydration upon warming provides the desired products with short overall reaction times. The successful use of nonactivated and halogenated phenethylene derived amides, N-vinyl amides, and optically active substrates is noteworthy.

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