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68485-15-4

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68485-15-4 Usage

General Description

2-Benzyloxazole is a chemical compound with the molecular formula C14H11NO. It is a heterocyclic compound consisting of a five-membered ring containing one nitrogen and one oxygen atom. 2-Benzyloxazole is mainly used as a building block in the synthesis of pharmaceuticals and agrochemicals. It can also be used as a fluorescent probe in biochemical studies. Additionally, 2-Benzyloxazole has been investigated for its potential application in organic electronics due to its semiconducting properties. This chemical is considered to be relatively safe for handling and has low toxicity, making it a versatile and useful compound in various industries.

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 articles and documents

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

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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