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154020-14-1

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154020-14-1 Usage

Structure

A five-membered heterocyclic organic compound containing nitrogen, oxygen, and carbon atoms in its ring structure.

Derivative

1,2,4-Oxadiazol-5-amine,3-ethoxy-(9CI) is a derivative of oxadiazole.

Substituent

An ethoxy group attached to the 3-position of the oxadiazole ring.

Potential applications

Pharmaceutical and agrochemical industries.

Biological activities

May exhibit biological activities useful for drug discovery or crop protection.

Further research

Additional research and testing may be required to fully understand its properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 154020-14-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,0,2 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 154020-14:
(8*1)+(7*5)+(6*4)+(5*0)+(4*2)+(3*0)+(2*1)+(1*4)=81
81 % 10 = 1
So 154020-14-1 is a valid CAS Registry Number.

154020-14-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-amino-3-ethoxy-2,3-dihydro-1,2,4-oxadiazol-3-one

1.2 Other means of identification

Product number -
Other names 5-amino-3-ethoxy-1,2,4-oxadiazole

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:154020-14-1 SDS

154020-14-1Relevant articles and documents

The Reaction of N-Cyanocarbonimidate and Related Compounds with Hydroxylamine

Suyama, Takayuki,Ozawa, Nobuyuki,Suzuki, Noriyuki

, p. 307 - 308 (1994)

O-ethyl S-methyl N-cyanocarbonimidothioate reacted with hydroxylamine to give 5-amino-3-ethoxy-1,2,4-oxadiazole, whereas diethyl N-cyanocarbonimidate reacted to give 3-amino-5-ethoxy-1,2,4-oxadiazole.The reaction of ethyl N-cyanocarbamate or S-methyl N-cyanothiocarbamate with hydroxylamine afforded 3-amino-1,2,4-oxadiazol-5(4H)-one.

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