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4,5-dibroMo-2-phenyl-1,3-oxazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92629-12-4

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92629-12-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92629-12-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,6,2 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 92629-12:
(7*9)+(6*2)+(5*6)+(4*2)+(3*9)+(2*1)+(1*2)=144
144 % 10 = 4
So 92629-12-4 is a valid CAS Registry Number.

92629-12-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-dibromo-2-phenyl-1,3-oxazole

1.2 Other means of identification

Product number -
Other names Oxazole,4,5-dibromo-2-phenyl

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:92629-12-4 SDS

92629-12-4Downstream Products

92629-12-4Relevant academic research and scientific papers

First halogen dance reaction on oxazoles. Synthesis of 4,5-disubstituted 2-phenyloxazoles

Stanetty, Peter,Spina, Markus,Mihovilovic, Marko D.

, p. 1433 - 1434 (2007/10/03)

The halogen dance reaction was investigated on the oxazole system for the first time. Various 5-substituted 4-bromo-2-phenyloxazole derivatives are accessible via this convenient methodology. Georg Thieme Verlag Stuttgart.

SYNTHESIS AND SOME ELECTROPHILIC SUBSTITUTION REACTIONS OF 2-PHENYLOXAZOLE

Belen'kii, L. I.,Cheskis, M. A.

, p. 713 - 716 (2007/10/02)

A new synthesis of 2-phenyloxazole that includes the preparation of 2-phenyloxazoline and aromatization of the latter by the action of nickel peroxide was developed.It was established that under conditions that exclude protonation electrophilic substituti

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