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Oxazole, 2,2'-(1,3-phenylene)bis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

101614-49-7

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101614-49-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101614-49-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,6,1 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 101614-49:
(8*1)+(7*0)+(6*1)+(5*6)+(4*1)+(3*4)+(2*4)+(1*9)=77
77 % 10 = 7
So 101614-49-7 is a valid CAS Registry Number.

101614-49-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-bis(2-oxazolinyl)benzene

1.2 Other means of identification

Product number -
Other names 1,3-bis(oxazol-2-yl)benzene

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:101614-49-7 SDS

101614-49-7Downstream Products

101614-49-7Relevant academic research and scientific papers

POLYCYCLIC COMPOUNDS AND METHODS OF MAKING AND USING THE SAME

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Page/Page column 168; 169, (2014/07/07)

The present disclosure provides compounds, or pharmaceutically acceptable salts thereof, for inhibiting the growth of a microbe; treating a mammal having a microbial infection, malaria, mucositis, an ophthalmic infection, an otic infection, a cancer, or a Mycobacterium infection; killing or inhibiting the growth of a Plasmodium species; inhibiting the growth of a Mycobacterium species; modulating an immune response in a mammal; or antagonizing unfractionated heparin, low molecular weight heparin, or a heparin/low molecular weight heparin derivative.

DDQ-induced dehydrogenation of heterocycles for c-c double bond formation: Synthesis of 2-thiazoles and 2-oxazoles

Li, Xiangnan,Li, Cheng,Yin, Bing,Li, Cong,Liu, Ping,Li, Jianli,Shi, Zhen

, p. 1408 - 1411 (2013/07/26)

Strong as an Ox: 2-Thiazoles and 2-oxazoles are formed by oxidation of 2-thiazolines and 2-oxazolines without requiring substituents at the C4 and C5 positions. DDQ plays an important role as the oxidant in this transformation and metal is unnecessary. This general procedure shows good functional group tolerance and provides a wide variety of 2-thiazoles and 2-oxazoles in moderate to excellent yields.

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