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4-(3-nitro-1H-1,2,4-triazol-1-yl)butan-2-one is a chemical compound with the molecular formula C7H10N4O3. It is a derivative of 1,2,4-triazole, a heterocyclic compound with a five-membered ring containing three nitrogen atoms. The compound features a butan-2-one (also known as methyl ethyl ketone) moiety, which is a four-carbon ketone with a carbonyl group at the second position. The 3-nitro-1H-1,2,4-triazol-1-yl group is attached to the fourth carbon of the butan-2-one chain, introducing a nitro group at the third position of the triazole ring. 4-(3-nitro-1H-1,2,4-triazol-1-yl)butan-2-one may have potential applications in the synthesis of pharmaceuticals, agrochemicals, or other chemical products due to its unique structure and reactivity.

60728-92-9

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60728-92-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60728-92-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,7,2 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 60728-92:
(7*6)+(6*0)+(5*7)+(4*2)+(3*8)+(2*9)+(1*2)=129
129 % 10 = 9
So 60728-92-9 is a valid CAS Registry Number.

60728-92-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(3-nitro-1,2,4-triazol-1-yl)butan-2-one

1.2 Other means of identification

Product number -
Other names 3-Nitro-1-(3-oxobutyl)-1,2,4-triazol

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:60728-92-9 SDS

60728-92-9Downstream Products

60728-92-9Relevant academic research and scientific papers

Nitration of triazolyl-substituted ketones

Kofman,Kartseva,Glazkova,Krasnov

, p. 753 - 757 (2005)

By nitration of 3-R-1,2,4-triazol-1-ylalkanones with a mixture of concentrated sulfuric and nitric acids a series of compounds was obtained containing a trinitromethyl fragment at the nitrogen of the ring. 2005 Pleiades Publishing, Inc.

THE ANIONS OF 1,2,4-TRIAZOLES. II. NUCLEOPHILIC REACTIVITY OF THE ANIONS OF 3-NITRO-5-1,2,4-TRIAZOLES IN ADDITION REACTIONS

Serov, Yu. V.,Pevzner, M. S.,Kofman, T. P.,Tselinskii, I. V.

, p. 1170 - 1173 (2007/10/02)

The kinetics of the reaction of a series of anions of 3-nitro-5-R-1,2,4-triazoles with methyl vinyl ketone in aqueous buffer solutions were studied.The logarithms of the rate constants correlate with the δJ0 constants of the substituents, and this indicates a predominant induction mechanism for the transmission of the effect of the substituents.The negative values of the entropy of activation demonstrate the rigidity of the transition state, and this leads to a decrease in the reactivity of the respective anions.

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