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103418-56-0

103418-56-0

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103418-56-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103418-56-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,4,1 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 103418-56:
(8*1)+(7*0)+(6*3)+(5*4)+(4*1)+(3*8)+(2*5)+(1*6)=90
90 % 10 = 0
So 103418-56-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H4N2O3/c9-6-8-7-5(11-6)4-2-1-3-10-4/h1-3H,(H,8,9)

103418-56-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(furan-2-yl)-3H-1,3,4-oxadiazol-2-one

1.2 Other means of identification

Product number -
Other names 2-(2'-furyl)-5-oxo-1,3,4-oxadiazoline

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:103418-56-0 SDS

103418-56-0Relevant articles and documents

-

Yale et al.

, p. 2208,2210 (1954)

-

Palladium-catalyzed oxidative O-H/N-H carbonylation of hydrazides: Access to substituted 1,3,4-oxadiazole-2(3 H)-ones

Ji, Fanghua,Li, Xianwei,Guo, Wei,Wu, Wanqing,Jiang, Huanfeng

, p. 5713 - 5718 (2015/06/16)

A novel palladium-catalyzed oxidative annulation reaction for the C-O, C-N bond formations is developed. The intramolecular cyclocarbonylation provides an efficient and direct approach for the construction of valuable 1,3,4-oxadiazole-2(3H)-ones and their

Efficient phosphonium-mediated synthesis of 2-amino-1,3,4-oxadiazoles

Levins, Christopher G.,Wan, Zhao-Kui

supporting information; experimental part, p. 1755 - 1758 (2009/04/12)

We present an efficient, room temperature procedure for the preparation of 2-amino-1,3,4-oxadiazoles. Oxadiazol-2-ones can be activated for SnAr substitution using phosphonium reagents (e.g., BOP). This approach provides convenient access to N,

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