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85681-47-6

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85681-47-6 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 17 carbon (C) atoms, 15 hydrogen (H) atoms, 3 nitrogen (N) atoms, and 1 oxygen (O) atom.

Explanation

Phenyl-1,2,4-triazoles are a class of organic compounds that contain a 1,2,4-triazole ring fused with a phenyl group. This class of compounds is known for their diverse range of applications.

Explanation

A heterocyclic aromatic compound is a compound that contains a ring of atoms with at least one atom being a heteroatom (an atom other than carbon). In this case, the 1,2,4-triazole ring contains three nitrogen atoms, making it a heterocyclic aromatic compound.

Explanation

The 1,2,4-triazole ring is a five-membered ring that consists of three nitrogen atoms and two carbon atoms. This structure is characteristic of the triazole class of compounds.

Explanation

The compound has a 5-phenyl-3-(5-methoxy-2-methylphenyl) group attached to the triazole ring. This specific arrangement of substituents gives the compound its unique physical and chemical properties.

Explanation

Due to its unique structure and properties, 1H-1,2,4-Triazole, 3-(5-methoxy-2-methylphenyl)-5-phenylhas potential applications in various fields. It can be used in the development of new drugs and agrochemicals, as well as in academic research for the synthesis of new materials and compounds.

Explanation

The presence of the 5-phenyl-3-(5-methoxy-2-methylphenyl) group in the compound affects its physical and chemical properties, such as solubility, reactivity, and stability. These properties can be further investigated and exploited for various applications.

Class

Phenyl-1,2,4-triazoles

Heterocyclic Aromatic Compound

Yes

Ring Structure

Five-membered ring with three nitrogen atoms and two carbon atoms

Substituents

5-Phenyl-3-(5-methoxy-2-methylphenyl) group

Potential Applications

Pharmaceutical and agrochemical industries, academic research for new materials and compounds

Physical and Chemical Properties

Influenced by the 5-phenyl-3-(5-methoxy-2-methylphenyl) group

Check Digit Verification of cas no

The CAS Registry Mumber 85681-47-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,6,8 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 85681-47:
(7*8)+(6*5)+(5*6)+(4*8)+(3*1)+(2*4)+(1*7)=166
166 % 10 = 6
So 85681-47-6 is a valid CAS Registry Number.

85681-47-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(5-methoxy-2-methylphenyl)-3-phenyl-1H-1,2,4-triazole

1.2 Other means of identification

Product number -
Other names 3-(5-METHOXY-2-METHYLPHENYL)-5-PHENYL-1H-1,2,4-TRIAZOLE

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:85681-47-6 SDS

85681-47-6Downstream Products

85681-47-6Relevant articles and documents

A New Class of Nonhormonal Pregnancy-Terminating Agents. Synthesis and Contragestational Activity of 3,5-Diaryl-s-triazoles

Omodei-Sale, Amedeo,Consonni, Pietro,Galliani, Giulio

, p. 1187 - 1192 (2007/10/02)

A series of 3,5-diaryl-s-triazoles were synthesized and evaluated as postimplantation contragestational agents.The introduction of various substituents (e.g., an o-alkyl chain on one phenyl and a m-alkoxy group on the other) was found to increase the potency.Several compounds with very high pregnancy-terminating activity in both hamsters and rats were obtained.One of these, 3-(2-ethylphenyl)-5-(3-methoxyphenyl)-s-triazole, DL 111 (36), was selected for detailed evaluation in various animal species.A synthetic scheme for the preparation of these compounds and preliminary structure-activity relationships are presented.

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