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ethyl 3-iodo-1-methyl-1H-pyrazole-4-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

799835-39-5

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799835-39-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 799835-39-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,9,8,3 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 799835-39:
(8*7)+(7*9)+(6*9)+(5*8)+(4*3)+(3*5)+(2*3)+(1*9)=255
255 % 10 = 5
So 799835-39-5 is a valid CAS Registry Number.

799835-39-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-iodo-1-methyl-1H-pyrazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names -

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:799835-39-5 SDS

799835-39-5Relevant academic research and scientific papers

INHIBITORS OF RIP1 KINASE AND METHODS OF USE THEREOF

-

, (2018/07/04)

The invention provides novel compounds having RIP1 kinase inhibitory activity, pharmaceutical compositions including the compounds and methods of using the compounds.

CALPAIN MODULATORS AND THERAPEUTIC USES THEREOF

-

Paragraph 1401, (2018/04/17)

Disclosed herein are small molecule calpain modulator compositions, pharmaceutical compositions, the use and preparation thereof.

A Michael Equilibration Model to Control Site Selectivity in the Condensation toward Aminopyrazoles

Fandrick, Daniel R.,Sanyal, Sanjit,Kaloko, Joseph,Mulder, Jason A.,Wang, Yuwen,Wu, Ling,Lee, Heewon,Roschangar, Frank,Hoffmann, Matthias,Senanayake, Chris H.

supporting information, p. 2964 - 2967 (2015/06/30)

A Michael equilibration model is presented to provide for site-selective pyrazole condensations between alkoxyacrylonitriles and hydrazines. Both pyrazole isomers were accessed with high selectivity by employment of kinetically or thermodynamically controlled conditions. Substrate scope and identification of Michael intermediates, as well as competitive pathways, support the presented mechanistic proposal. Sandmeyer derivatization provided site-selective access to fully substituted pyrazoles.

Iodopyrazolyl carboxanilides

-

, (2008/06/13)

This invention relates to novel iodopyrazolylcarboxanilides of the formula (I) t,0010 in which R1, R2, R3, R4, R5, R6 and Z are as defined in the disclosure, to a plurality of processes for preparing these compounds and to their use for controlling unwanted microorganisms. This invention further relates to novel intermediates and their preparation.

IODOPYRAZOLYL CARBOXANILIDES

-

Page/Page column 54, (2008/06/13)

The invention relates to iodopyrazolyl carboxanilides of formula (I), in which R1, R2, R3, R4, R5, R6 and Z are defined as cited in the description. The invention also relates to several methods for producing said substances and to the use of the latter for controlling undesired micro-organisms, in addition to novel intermediate products and their production.

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