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1H-1,2,3-Triazole, 4,5-dihydro-5-(3-nitrophenyl)-1-phenyl- is a complex organic compound with the molecular formula C15H12N4O2. It is a derivative of 1,2,3-triazole, a five-membered heterocyclic ring containing three nitrogen atoms. The compound features a 4,5-dihydro-1-phenyl-1H-1,2,3-triazole core, with a 3-nitrophenyl group attached at the 5-position. This nitro group imparts a strong electron-withdrawing effect, which can influence the compound's reactivity and stability. The phenyl group at the 1-position provides additional aromatic character to the molecule. This specific arrangement of functional groups makes it a potentially useful building block in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals, where its unique electronic properties can be exploited for specific applications.

10445-20-2

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10445-20-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10445-20-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,4 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10445-20:
(7*1)+(6*0)+(5*4)+(4*4)+(3*5)+(2*2)+(1*0)=62
62 % 10 = 2
So 10445-20-2 is a valid CAS Registry Number.

10445-20-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(3-nitro-phenyl)-1-phenyl-4,5-dihydro-1H-[1,2,3]triazole

1.2 Other means of identification

Product number -
Other names 1-Phenyl-5-(3-nitro-phenyl)-1,2,3-triazolin

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:10445-20-2 SDS

10445-20-2Downstream Products

10445-20-2Relevant academic research and scientific papers

Triazolines. XXXIX. 1,5-Diaryl-δ2-1,2,3-triazolines as Aphicides: Mechanism of Action via Aziridine Formation

Kadaba, Pankaja K.

, p. 299 - 304 (2007/10/03)

The aphicidal activity of 21 different 1,5-diphenyl-Δ2-1,2,3-triazolines, conveniently prepared utilizing the catalytic effect of water on the 1,3-cycloaddition of diazomethane to Shiff bases in aqueous dioxane, was evaluated. Triazolines beari

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