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140706-49-6

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140706-49-6 Usage

General Description

1,2,5-Oxadiazole-3,4-diamine,N-ethyl-(9CI) is a chemical compound with the molecular formula C4H8N4O. It is also known by its CAS number 15533-79-4. 1,2,5-Oxadiazole-3,4-diamine,N-ethyl-(9CI) is a type of oxadiazole, which is a five-membered aromatic ring with three nitrogen atoms and two carbon atoms. 1,2,5-Oxadiazole-3,4-diamine,N-ethyl-(9CI) is an amine derivative, meaning it contains one or more amino groups. Its N-ethyl group indicates the presence of an ethyl substituent on the nitrogen atom of the amine. This chemical compound has potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science, due to its unique structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 140706-49-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,7,0 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 140706-49:
(8*1)+(7*4)+(6*0)+(5*7)+(4*0)+(3*6)+(2*4)+(1*9)=106
106 % 10 = 6
So 140706-49-6 is a valid CAS Registry Number.

140706-49-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Ethyl-furazan-3,4-diamine

1.2 Other means of identification

Product number -
Other names -

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:140706-49-6 SDS

140706-49-6Downstream Products

140706-49-6Relevant articles and documents

Potential histamine H2-receptor antagonist: Synthesis and pharmacological activity of derivatives containing acylamino-furazan moieties

Sorba,Fruttero,Di Stilo,Gasco,Orsetti

, p. 151 - 155 (2007/10/02)

Analogues of 3-amino-4-[2-[(5-dimethylaminomethyl-2-furyl)methylthio]ethylamino]fura zan (1) containing carbonyl groups joined to the amino functions linked to the furazan system have been synthetized and investigated for their H2-antagonist pr

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