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110525-56-9

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110525-56-9 Usage

General Description

4-(1H-pyrazol-1-yl)butanoic acid, also known as SALTDATA: FREE, is a chemical compound with the molecular formula C8H10N2O2. It is a pyrazole derivative and contains a butanoic acid group. 4-(1H-pyrazol-1-yl)butanoic acid(SALTDATA: FREE) is used in various pharmaceutical and biochemical applications, including as a building block for the synthesis of more complex molecules. It may also have potential therapeutic properties, although further research is needed to fully understand its biological activity and potential medical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 110525-56-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,5,2 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 110525-56:
(8*1)+(7*1)+(6*0)+(5*5)+(4*2)+(3*5)+(2*5)+(1*6)=79
79 % 10 = 9
So 110525-56-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H10N2O2/c10-7(11)3-1-5-9-6-2-4-8-9/h2,4,6H,1,3,5H2,(H,10,11)

110525-56-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-pyrazol-1-ylbutanoic acid

1.2 Other means of identification

Product number -
Other names 4-(1H-pyrazol-1-yl)butanoic acid

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 -
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More Details:110525-56-9 SDS

110525-56-9Relevant articles and documents

Novel Parham-type Cycloacylations of 1H-Pyrazole-1-alkanoic Acids

Larsen, Scott D.

, p. 1013 - 1014 (2007/10/03)

Exposure of 1H-pyrazole-1-alkanoic acids to two equivalents of n-butyllithium affords the corresponding cyclic ketones via a Parham-type cyclization process. Although yields are modest, this procedure represents a simple and direct intramolecular acylation of a non-nucleophilic pyrazole carbon.

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