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3,4-Diiodo-5-methyl-1H-pyrazole is a pyrazole derivative with the molecular formula C4H5I2N. It features a pyrazole ring with two iodine atoms attached at the 3 and 4 positions and a methyl group at the 5 position. This chemical compound is mainly utilized in research and laboratory settings.
Used in Research and Laboratory Settings:
3,4-Diiodo-5-methyl-1H-pyrazole is used as a building block for the synthesis of other organic compounds, contributing to the development of new chemical entities and materials.
Used in Pharmaceutical Industry:
3,4-Diiodo-5-methyl-1H-pyrazole may be employed as a precursor or intermediate in the development of pharmaceuticals, leveraging its unique structure and reactivity for potential therapeutic applications.
Used in Agrochemical Industry:
Similarly, in the agrochemical sector, 3,4-Diiodo-5-methyl-1H-pyrazole could serve as a starting material for the synthesis of new agrochemicals, potentially leading to innovative products for agricultural use.
However, it is important to note that the specific properties and potential uses of 3,4-Diiodo-5-methyl-1H-pyrazole have not been extensively studied or documented in the scientific literature, indicating a need for further research to fully explore its capabilities and applications.

6715-87-3

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6715-87-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6715-87-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,1 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6715-87:
(6*6)+(5*7)+(4*1)+(3*5)+(2*8)+(1*7)=113
113 % 10 = 3
So 6715-87-3 is a valid CAS Registry Number.

6715-87-3SDS

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 3,4-diiodo-5-methyl-1H-pyrazole

1.2 Other means of identification

Product number -
Other names 3,4-Diod-5-methyl-pyrazol

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:6715-87-3 SDS

6715-87-3Upstream product

6715-87-3Relevant academic research and scientific papers

ORGANIC COMPOUNDS

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Page/Page column 112, (2008/06/13)

The present invention provides heterocyclic derivatives that modulate the activity of stearoyl-CoA desaturase. Methods of using such derivatives to modulate the activity of stearoyl-CoA desaturase and pharmaceutical compositions comprising such derivatives are also encompassed.

Micelle Activated Reactions I. Micelle Activated Iodination and Partial Dehalogenation of Pyrazoles and 1,2,4-Triazoles

Miethchen, R.,Randow, R.,Listemann, R.,Hildebrandt, J.,Kohlheim, K.

, p. 799 - 805 (2007/10/02)

A method is described to iodinate pyrazole, substituted pyrazoles or 1,2,4-triazole with iodine or iodine chloride in aqueous alkaline in the presence of an anionic surfactant. 4-Iodo- (2a), 4-iodo-3(5)-methyl- (2b), 3(5),4-diiodo- (3a), 3(5),4-diiodo-5(3)-methyl- (3b), and 3,4,5-triiodo-pyrazole (3d) as soon as 4-iodo-pyrazole-3(5)-carboxylic acid (2c), and 3(5)-iodo-1,2,4-triazole (5) were prepared.Anhydrous hydrogen fluoride or triethylamine trishydrofluoride were found to be a suitable agent to effect a regioselective partial dehalogenation of 3b, 3d and 3,5-dibromo-1,2,4-triazole (7).We prepared 3(5)-iodo-5(3)-methyl-pyrazole (6b), 3,5-diiodo-pyrazole (6d) and 3(5)-bromo-1,2,4-triazole (8) on this way.

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