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1-Benzyl-1H-pyrazol-3-ylamine, a pyrazole derivative with the molecular formula C11H12N4, is an aminopyrazole compound characterized by the presence of a pyrazole ring and an amine group. This chemical compound has garnered interest due to its potential applications in pharmaceuticals and agrochemicals, serving as a building block in the synthesis of various drugs and crop protection agents. Additionally, it exhibits biological activity and is under investigation for its pharmacological properties, with ongoing research aimed at uncovering its full potential.

21377-09-3

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21377-09-3 Usage

Uses

Used in Pharmaceutical Industry:
1-Benzyl-1H-pyrazol-3-ylamine is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows it to be incorporated into drug molecules, potentially enhancing their therapeutic effects and targeting specific biological pathways.
Used in Agrochemical Industry:
In the agrochemical sector, 1-benzyl-1H-pyrazol-3-ylamine is utilized as a building block in the development of crop protection agents. Its incorporation into these agents can lead to improved efficacy in protecting crops from pests and diseases, thereby contributing to increased agricultural productivity.
Used in Research and Development:
1-Benzyl-1H-pyrazol-3-ylamine is employed as a subject of research in the exploration of its biological activity and pharmacological properties. Scientists are investigating its potential uses in the development of new drugs and therapies, as well as its interactions with biological systems to better understand its mechanisms of action.

Check Digit Verification of cas no

The CAS Registry Mumber 21377-09-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,3,7 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 21377-09:
(7*2)+(6*1)+(5*3)+(4*7)+(3*7)+(2*0)+(1*9)=93
93 % 10 = 3
So 21377-09-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H11N3/c11-10-6-7-13(12-10)8-9-4-2-1-3-5-9/h1-7H,8H2,(H2,11,12)

21377-09-3 Well-known Company Product Price

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  • Aldrich

  • (CBR00217)  1-Benzyl-1H-pyrazol-3-amine  AldrichCPR

  • 21377-09-3

  • CBR00217-1G

  • 2,767.05CNY

  • Detail

21377-09-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzylpyrazol-3-amine

1.2 Other means of identification

Product number -
Other names 1-(phenylmethyl)-1H-pyrazol-3-amine

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:21377-09-3 SDS

21377-09-3Relevant academic research and scientific papers

Synthesis and properties of 1-[(adamantan-1-yl)methyl]-3-pyrazolyl ureas

D’yachenko, Vladimir S.,Danilov, Dmitry V.,Shkineva, Tatyana K.,Vatsadze, Irina А.,Burmistrov, Vladimir V.,Butov, Gennady M.

, p. 129 - 134 (2019/04/13)

[Figure not available: see fulltext.] A series of 1,3-disubstituted ureas containing 1,3,5-trisubstituted pyrazole and (adamantan-1-yl)methyl fragments were synthesized in the reaction of 1-(isocyanatomethyl)adamantane with 3- or 4-aminopyrazoles under mi

SULFONYLUREAS AND RELATED COMPOUNDS AND USE OF SAME

-

, (2016/09/15)

ABSTRACT The present invention provides for certain sulfonyl ureas and related compounds which have advantageous properties and show useful activity in the inhibition of activation of the NLRP3 inflammasome. Such compounds are useful in the treatment of a wide range of disorders in which the inflammation process, or more specifically the NLRP3 inflammasome, have been implicated as being a key factor.

(PYRAZOL-3-YL)-1,3,4-THIADIAZOL-2-AMINE AND (PYRAZOL-3-YL)-1,3,4-THIAZOL-2-AMINE COMPOUNDS

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Page/Page column 23, (2012/04/23)

A compound of Formula (I) wherein: either X is N and Y is CR5 or X is C and Y is S; Z is selected from N and CH; R1 is selected from H and Me; R2 is selected from H, OH, OMe and Me; each R3 is independently selected from C1-3alkyl, F, Cl, Br, CF3 and NH2; R4 is selected from Me, CF3, NO2 and CHF2; R5 is selected from H, Me and CHF2; R6 is selected from H and Me; and p is 0-3, compositions containing them, their use in therapy, for example in the treatment of tuberculosis, and methods for the preparation of such compounds, are provided.

N- ( PYRAZOLE- 3 -YL) -BENZAMIDE DERIVATIVES AS GLUCOKINASE ACTIVATORS

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Page/Page column 49-50, (2009/05/30)

Novel heterocyclic compounds of the formula (I) in which R1, R2, R3, R4, R5, R6, R7, Alk and D have the meanings indicate in Claim 1, are activators of glucokinase and can be used for the prevention and/or treatment of Diabetes Typ 1 and 2, obesity, neuropathy and/or nephropathy.

Pyrazole glucokinase activators

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, (2008/06/13)

Disclosed herein are pyrazole glucokinase activators of the formula (I) useful for the treatment of metabolic diseases and disorders, preferably diabetes mellitus.

Substituted 1H-pyrazolo (1,5-a) pyrimidines and process for their preparation

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, (2008/06/13)

Compounds of general formula (I) STR1 wherein R1 is a 2-pyridyl, 3-pyridyl or 4-pyridyl group; (b) a phenyl ring, unsubstituted or substituted by one or two groups chosen from halogen, trihalo-C1 -C4 alkyl, C1 -

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