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2-Benzyloxazole is a heterocyclic chemical compound with the molecular formula C14H11NO. It features a five-membered ring structure that includes one nitrogen and one oxygen atom. Known for its semiconducting properties, low toxicity, and relative safety in handling, 2-Benzyloxazole serves as a versatile building block in various industries.

68485-15-4

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68485-15-4 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
2-Benzyloxazole is utilized as a key building block in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure and properties make it a valuable component in the development of new drugs and agricultural chemicals.
Used in Biochemical Research:
As a fluorescent probe, 2-Benzyloxazole is employed in biochemical studies. Its ability to emit fluorescence under certain conditions allows researchers to track and monitor biological processes, contributing to a better understanding of cellular and molecular mechanisms.
Used in Organic Electronics:
2-Benzyloxazole has been investigated for its potential application in the field of organic electronics. Its semiconducting properties make it a promising candidate for use in the development of electronic devices, such as organic light-emitting diodes (OLEDs) and organic solar cells.

Check Digit Verification of cas no

The CAS Registry Mumber 68485-15-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,4,8 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 68485-15:
(7*6)+(6*8)+(5*4)+(4*8)+(3*5)+(2*1)+(1*5)=164
164 % 10 = 4
So 68485-15-4 is a valid CAS Registry Number.

68485-15-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzyl-oxazole

1.2 Other means of identification

Product number -
Other names 2-benzyloxazole

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:68485-15-4 SDS

68485-15-4Relevant academic research and scientific papers

Nickel-catalyzed synthesis of oxazoles via C-S activation

Lee, Kyoungsoo,Counceller, Carla M.,Stambuli, James P.

supporting information; experimental part, p. 1457 - 1559 (2009/08/08)

The synthesis of 2-substituted oxazoles is achieved via nickel-catalyzed cross-coupling reaction of 2-methylthio-oxazole and various organozinc reagents. An extension of this method is demonstrated with a chemoselective, one-pot synthesis of unsymmetrical

Diheteroarylmethanes. 5. E-Z isomerism of carbanions substituted by 1,3-Azoles: 13C and 15N π-charge/shift relationships as source for mapping charge and ranking the electron-withdrawing power of heterocycles

Abbotto, Alessandro,Bradamante, Silvia,Pagani, Giorgio A.

, p. 1761 - 1769 (2007/10/03)

Previously proposed π-charge/shift relationships have been applied to 13C and 15N shifts of the carbanions of 2-benzylazoles (thiazole, oxazole, and imidazole), their corresponding benzo-fused analogs, and bis(2-azolyl)methanes (azol

Pyridin-3-ols

-

, (2008/06/13)

New pyridin-3-ols and their N-oxides and acid addition salts, which are useful as intermediates, especially for the preparation of pharmacologically active compounds, and their preparation.

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