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METHYL-(2H-PYRAZOL-3-YLMETHYL)-AMINE, with the molecular formula C6H10N2, is a pyrazole derivative characterized by a five-membered aromatic ring with two nitrogen atoms. This chemical compound serves as a versatile building block in organic synthesis, particularly for the creation of pharmaceuticals and agrochemicals. Its unique structure and reactivity contribute to its value as an intermediate for preparing a wide array of biologically active molecules. Beyond its applications in the synthesis of various compounds, METHYL-(2H-PYRAZOL-3-YLMETHYL)-AMINE also finds use in the production of fine chemicals, dyes, and pigments, and as a reagent in chemical research and laboratory experiments.

676491-02-4

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676491-02-4 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
METHYL-(2H-PYRAZOL-3-YLMETHYL)-AMINE is used as a building block for the synthesis of various pharmaceuticals and agrochemicals, leveraging its reactivity and structural properties to create molecules with potential biological activities.
Used in Fine Chemicals Production:
METHYL-(2H-PYRAZOL-3-YLMETHYL)-AMINE is used as a component in the production of fine chemicals, contributing to the development of high-quality specialty chemicals for various applications.
Used in Dyes and Pigments Industry:
METHYL-(2H-PYRAZOL-3-YLMETHYL)-AMINE is utilized in the formulation of dyes and pigments, enhancing the color properties and performance of these products in different industries.
Used as a Reagent in Chemical Research:
METHYL-(2H-PYRAZOL-3-YLMETHYL)-AMINE is employed as a reagent in chemical research and laboratory experiments, facilitating the exploration of new chemical reactions and the development of novel compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 676491-02-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,6,4,9 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 676491-02:
(8*6)+(7*7)+(6*6)+(5*4)+(4*9)+(3*1)+(2*0)+(1*2)=194
194 % 10 = 4
So 676491-02-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H9N3/c1-6-4-5-2-3-7-8-5/h2-3,6H,4H2,1H3,(H,7,8)

676491-02-4SDS

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 N-methyl-1-(1H-pyrazol-5-yl)methanamine

1.2 Other means of identification

Product number -
Other names 3-methylaminomethyl-2h-pyrazole

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:676491-02-4 SDS

676491-02-4Relevant academic research and scientific papers

SUBSTITUTED PYRIDINES AS INHIBITORS OF DNMT1

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Page/Page column 969, (2018/01/20)

The invention is directed to substituted pyridine derivatives. Specifically, the invention is directed to compounds according to Formula (Iar): (Iar) wherein Yar, X1ar, X2ar, R1ar, R2ar, R3ar, R4ar and R5ar are as defined herein; or a pharmaceutically acceptable salt or prodrug thereof. The compounds of the invention are selective inhibitors of DNMT1 and can be useful in the treatment of cancer, pre-cancerous syndromes, beta hemoglobinopathy disorders, sickle cell disease, sickle cell anemia, and beta thalassemia, and diseases associated with DNMT1 inhibition. Accordingly, the invention is further directed to pharmaceutical compositions comprising a compound of the invention. The invention is still further directed to methods of inhibiting DNMT1 activity and treatment of disorders associated therewith using a compound of the invention or a pharmaceutical composition comprising a compound of the invention.

Composition and antiviral activity of substituted azaindoleoxoacetic piperazine derivatives

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Page 184, (2008/06/13)

This invention provides compounds having drug and bio-affecting properties, their pharmaceutical compositions and method of use. In particular, the invention is concerned with azaindoleoxoacetyl piperazine derivatives. These compounds possess unique antiviral activity, whether used alone or in combination with other antivirals, antiinfectives, immunomodulators or HIV entry inhibitors. More particularly, the present invention relates to the treatment of HIV and AIDS.

Indole, azaindole and related heterocyclic 4-alkenyl piperidine amides

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Page/Page column 91, (2010/02/06)

This invention provides compounds having drug and bio-affecting properties, their pharmaceutical compositions and method of use. In particular, the invention is concerned with new piperidine 4-alkenyl derivatives that possess unique antiviral activity. More particularly, the present invention relates to compounds useful for the treatment of HIV and AIDS. The compounds of the invention for the general Formula I: wherein: Z is Q is selected from the group consisting of: —W— is

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