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2-Oxazolebutanal, 4,5-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91621-02-2

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91621-02-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91621-02-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,6,2 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 91621-02:
(7*9)+(6*1)+(5*6)+(4*2)+(3*1)+(2*0)+(1*2)=112
112 % 10 = 2
So 91621-02-2 is a valid CAS Registry Number.

91621-02-2SDS

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 2-(4-oxobutyl)-4,5-diphenyloxazole

1.2 Other means of identification

Product number -
Other names -

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:91621-02-2 SDS

91621-02-2Relevant academic research and scientific papers

ASYMMETRIC EPOXIDATION OF ALLYLIC ALCOHOLS EMPLOYING 4,5-DIPHENYLOXAZOLE AS A MASKED ESTER FUNCTIONALITY

Pridgen, Lendon N.,Shilcrat, S. C.,Lantos, I.

, p. 2835 - 2838 (2007/10/02)

The 4,5-diphenyloxazolyl moiety has been found to be a masked ester functionality fully compatible with the Sharpless epoxidation of allylic alcohols within the same molecule.

Synthesis of 1,2-Polymethyleneimidazoles Utilizing Intramolecular Ring Transformation

Sasaki, Tadashi,Ohno, Masatomi,Ito, Eikoh

, p. 899 - 900 (2007/10/02)

Among the intramolecular cyclodehydration of 2-(β-, δ-, and ε-aminoalkyl)oxazoles, 2-(δ-aminoalkyl)oxazoles afforded the desired 1,2-tetramethyleneimidazoles on pyrolysis, while 2-(β- and ε-aminoalkyl)oxazoles unchanged under the same conditions.

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