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5543-33-9

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5543-33-9 Usage

General Description

(3-phenyl-1,2,4-oxadiazol-5-yl)methanol is a chemical compound with the molecular formula C9H7N3O2. It is a white solid with a molecular weight of 189.17 g/mol. (3-phenyl-1,2,4-oxadiazol-5-yl)methanol is a derivative of oxadiazole and is commonly used as a building block in organic synthesis. It has potential applications in the pharmaceutical industry for the development of new drugs and in the field of material science for the design of novel materials. Additionally, (3-phenyl-1,2,4-oxadiazol-5-yl)methanol may also have utility as a fluorescent probe in biological studies and as a ligand in coordination chemistry. Overall, this compound has versatile uses and potential for further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 5543-33-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,4 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5543-33:
(6*5)+(5*5)+(4*4)+(3*3)+(2*3)+(1*3)=89
89 % 10 = 9
So 5543-33-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H8N2O2/c12-6-8-10-9(11-13-8)7-4-2-1-3-5-7/h1-5,12H,6H2

5543-33-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-phenyl-1,2,4-oxadiazol-5-yl)methanol

1.2 Other means of identification

Product number -
Other names 5-Hydroxymethyl-3-phenyl-1,2,4-oxadiazol

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:5543-33-9 SDS

5543-33-9Downstream Products

5543-33-9Relevant articles and documents

Construction of 3,5-substituted 1,2,4-oxadiazole rings triggered by tetrabutylammonium hydroxide: A highly efficient and fluoride-free ring closure reaction of O-acylamidoximes

Otaka, Hiromichi,Ikeda, Junya,Tanaka, Daisuke,Tobe, Masanori

, p. 979 - 981 (2014/02/14)

Tetrabutylammonium hydroxide (TBAH) is an efficient and mild alternative to tetrabutylammonium fluoride (TBAF) for base catalyzed cyclizations of 1,2,4-oxadiazoles from O-acylamidoximes. For most 3,5-substituted 1,2,4-oxadiazoles the reactions were dramatically accelerated by addition of 0.1 equiv of TBAH at room temperature. This method was also more generally applicable allowing for a wider range of substrates. Additionally, due to the absence of fluoride, TBAH will not result in corrosion of reactor vessels and therefore is better suited for large-scale synthesis.

Metabolities of 3-phenyl-5-methyl-1,2,4-oxadiazole (PMO) in rats, dogs, and mice.

Schickedantz,Skladanowski,Zaletel,Marmor,Minnemeyer

, p. 876 - 881 (2007/10/05)

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