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56367-24-9

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56367-24-9 Usage

Uses

3-Isopropyl-1H-pyrazol-5-amine

Check Digit Verification of cas no

The CAS Registry Mumber 56367-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,3,6 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 56367-24:
(7*5)+(6*6)+(5*3)+(4*6)+(3*7)+(2*2)+(1*4)=139
139 % 10 = 9
So 56367-24-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H11N3/c1-4(2)5-3-6(7)9-8-5/h3-4H,1-2H3,(H3,7,8,9)

56367-24-9SDS

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 5-propan-2-yl-1H-pyrazol-3-amine

1.2 Other means of identification

Product number -
Other names 5-isopropyl-2H-pyrazol-3-ylamine

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:56367-24-9 SDS

56367-24-9Relevant articles and documents

Identification of TRD-35 as Potent and Selective DRAK2 Inhibitor

Ali, Imran,Park, Sangjun,Jung, Myoung Eun,Lee, Nari,Bibi, Maimoona,Chae, Chong Hak,Yang, Kyung-Min,Kim, Seong-Jin,Choi, Gildon,Lee, Kwangho

supporting information, p. 567 - 569 (2020/03/23)

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Synthesis of aminopyrazole analogs and their evaluation as CDK inhibitors for cancer therapy

Rana, Sandeep,Sonawane, Yogesh A.,Taylor, Margaret A.,Kizhake, Smitha,Zahid, Muhammad,Natarajan, Amarnath

supporting information, p. 3736 - 3740 (2018/10/24)

We synthesized a library of aminopyrazole analogs to systematically explore the hydrophobic pocket adjacent to the hinge region and the solvent exposed region of cyclin dependent kinases. Structure-activity relationship studies identified an optimal substitution for the hydrophobic pocket and analog 24 as a potent and selective CDK2/5 inhibitor.

Pyrazolotriazines as inhibitors of nucleases

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Paragraph 0122; 0123; 0124; 0125; 0126; 0127; 0145-0150, (2016/01/12)

The invention provides compounds represented by the structural formula (1): wherein R1, R2, R3 and R4 are as defined in the claims. The compounds are inhibitors of nucleases, and are useful in particular in a method of treatment and/or prevention of proliferative diseases, neurodegenerative diseases, and other genomic instability associated diseases.

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