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1H-Indazole, 5,7-dichloro-, with the molecular formula C7H4Cl2N2, is a chemical compound belonging to the class of indazoles. It features an aromatic heterocyclic structure with a five-membered ring containing two nitrogen atoms, and is distinguished by the presence of two chlorine atoms at the 5 and 7 positions of the indazole ring. 1H-Indazole, 5,7-dichlorois recognized for its potential in the synthesis of biologically active molecules, making it a valuable component in pharmaceutical and agrochemical development.

50477-27-5

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50477-27-5 Usage

Uses

Used in Pharmaceutical Industry:
1H-Indazole, 5,7-dichlorois used as a building block for the synthesis of biologically active molecules, serving as a key component in the creation of pharmaceutical drugs. Its unique structure and properties contribute to the development of new chemical entities aimed at addressing various therapeutic needs.
Used in Agrochemical Development:
In addition to its pharmaceutical applications, 1H-Indazole, 5,7-dichlorois also utilized in the agrochemical industry for the synthesis of biologically active compounds. Its role as a building block aids in the development of new agrochemicals designed to improve crop protection and yield.
Used in Medicinal Chemistry and Drug Discovery Research:
Due to its potential biological activity, 1H-Indazole, 5,7-dichlorois of significant interest in medicinal chemistry and drug discovery research. It serves as a valuable tool for exploring and understanding the mechanisms of action of new chemical entities, thereby contributing to the advancement of novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 50477-27-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,4,7 and 7 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 50477-27:
(7*5)+(6*0)+(5*4)+(4*7)+(3*7)+(2*2)+(1*7)=115
115 % 10 = 5
So 50477-27-5 is a valid CAS Registry Number.

50477-27-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,7-dichloro-1H-indazole

1.2 Other means of identification

Product number -
Other names 5,7-Dichlorindazol

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:50477-27-5 SDS

50477-27-5Downstream Products

50477-27-5Relevant academic research and scientific papers

ARYLOAZOL-2-YL CYANOETHYLAMINO COMPOUNDS, METHOD OF MAKING AND METHOD OF USING THEREOF

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Paragraph 0654, (2014/04/03)

The present invention relates to novel aryloazol-2-yl-cyanoethylamino derivatives of formula (I): wherein R3, R4, R5, R6, R7, P, Q, V, W, X, Y, Z and a are as defined in the description, compositions thereof, processes for their preparation and their uses as pesticides.

ENANTIOMERICALLY ENRICHED ARYLOAZOL-2-YL CYANOETHYLAMINO COMPOUNDS, METHOD OF MAKING AND METHOD OF USING THEREOF

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Page/Page column 69-70, (2010/06/13)

The present invention relates to novel aryloazol-2-yl-cyanoethylamino derivatives substantially enriched in an enantiomer of formula (I): and compounds of formula (IH) wherein R3, R4, R5, R6, R7, R13a, R13b, R14a, R14b, P, Q, V, W, X, Y, Z and a are as defined in the description, compositions thereof, processes for their preparation and their uses as pesticides.

ARYLOAZOL-2-YL CYANOETHYLAMINO COMPOUNDS, METHOD OF MAKING AND METHOD OF USING THEREOF

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Page/Page column 86, (2009/01/20)

The present invention relates to novel aryloazol-2-yl-cyanoethylamino derivatives of formula (I):wherein R3, R4, R5, R6, R7, P, Q, V, W, X, Y, Z and a are as defined in the description, compositions thereof, processes for their preparation and their uses as pesticides.

An efficient synthesis of 1-H indazoles

Lokhande,Raheem, Abdul,Sabale,Chabukswar,Jagdale

, p. 6890 - 6892 (2008/02/12)

The reaction of substituted salicyaldehydes with hydrazine hydrochloride under different conditions gave the corresponding 1-H indazoles. However, the reaction of benzaldehydes with hydrazine hydrate under the same conditions yielded only hydrazones.

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