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90253-22-8

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90253-22-8 Usage

General Description

4-cyclopentyl-1H-pyrazole is a chemical compound belonging to the class of pyrazoles, which are heterocyclic organic compounds containing a five-membered ring of four carbon atoms and one nitrogen atom. The addition of a cyclopentyl group to the pyrazole ring gives the compound its unique structure and properties. 4-cyclopentyl-1H-pyrazole is used in the synthesis of pharmaceuticals and agrochemicals due to its potential as a building block for more complex molecules. It has also been studied for its potential biological activities, including as an inhibitor of enzymes involved in disease processes. Also, 4-cyclopentyl-1H-pyrazole may be used in research and development activities for creating new compounds with desired properties. Overall, this chemical compound has potential applications in both the pharmaceutical and agrochemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 90253-22-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,2,5 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 90253-22:
(7*9)+(6*0)+(5*2)+(4*5)+(3*3)+(2*2)+(1*2)=108
108 % 10 = 8
So 90253-22-8 is a valid CAS Registry Number.

90253-22-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Cyclopentyl-1H-pyrazole

1.2 Other means of identification

Product number -
Other names 4-Cyclopentylpyrazol

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:90253-22-8 SDS

90253-22-8Downstream Products

90253-22-8Relevant articles and documents

Syntheses with Aliphatic Dialdehydes, XXXVIII. - Synthesis and Properties of Cycloalkylmalonaldehydes

Reichardt, Christian,Ferwanah, Abdel-Rahman,Pressler, Wilfried,Yun, Kyeong-Yeol

, p. 649 - 679 (2007/10/02)

Vilsmeier formylation of cycloalkyl-substituted enol ethers (7,14a - c,23) yields the cycloalkylmalonaldehydes 1 - 5 for the first time.In solution 1 - 5 exist in the (E)-s-(E) enol form as vinylogous carboxylic acids.The reaction of 1 - 5 with suitable electrophiles and nucleophiles leads to cycloalkyl-substituted open-chain (29,30), carbocyclic (31) as well as heterocyclic compounds (32-40) with peculiar properties due to the presence of the lipophilic cycloalkyl group.

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