3191-87-5 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
This describes the arrangement of atoms and the type of chemical bonds in the compound.
3. Pyrazole Carboxylic Acid Derivative
Explanation
The compound is derived from a pyrazole carboxylic acid, which is a five-membered ring containing four carbon atoms and one nitrogen atom, with a carboxylic acid group attached.
Explanation
A phenyl group (C6H5) is attached to the first carbon atom of the pyrazole ring, which is an aromatic ring consisting of six carbon atoms and five hydrogen atoms.
Explanation
An isopropyl group (C3H7) is attached to the fifth carbon atom of the pyrazole ring, which is a branched alkyl group consisting of three carbon atoms and seven hydrogen atoms.
Explanation
The compound may have potential uses in the development of new drugs or in chemical synthesis processes due to its unique structure and properties.
Explanation
The compound may be valuable for scientific research, particularly in the fields of medicinal chemistry and chemical biology, to study its properties and potential applications.
Explanation
As with any chemical compound, it is important to handle 1-(phenyl)-5-isopropyl-1H-pyrazole-3-carboxylic acid with care, as it may have certain hazards associated with its use, such as toxicity, flammability, or reactivity with other substances.
Explanation
When working with 1-(PHENYL)-5-ISOPROPYL-1H-PYRAZOLE-3-CARBOXYLIC ACID, it is essential to follow appropriate safety protocols, including the use of personal protective equipment (PPE) and working in a well-ventilated area or fume hood.
Chemical Structure
1-(phenyl)-5-isopropyl-1H-pyrazole-3-carboxylic acid
Phenyl Group Attachment
First carbon atom of the pyrazole ring
Isopropyl Group Attachment
Fifth carbon atom of the pyrazole ring
Potential Applications
Pharmaceutical and chemical synthesis
Research Utility
Useful for research purposes
Hazards
Handle with care
Safety Precautions
Follow proper safety protocols
Check Digit Verification of cas no
The CAS Registry Mumber 3191-87-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,9 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3191-87:
(6*3)+(5*1)+(4*9)+(3*1)+(2*8)+(1*7)=85
85 % 10 = 5
So 3191-87-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H14N2O2/c1-9(2)12-8-11(13(16)17)14-15(12)10-6-4-3-5-7-10/h3-9H,1-2H3,(H,16,17)
3191-87-5Relevant academic research and scientific papers
REACTION OF D-GALACTOSE PHENYLHYDRAZONE WITH NITROALKENES:SYNTHESIS OF PENTAHYDROXYPENTYLPYRAZOLES
Guillen, Manuel Gomez,Jiminez, Juan L. Conde
, p. 1 - 18 (2007/10/02)
D-Galactose phenylhydrazone reacts with 1- and 2-substituted and 1,2-disubstituted nitroalkenes, with loss of the nitro group, to give moderate yields of 3-(D-galacto-pentitol-1-yl)-1-phenylpyrazoles variously substituted at positins 4, 5 and a mechanism is proposed.Acetylation of these products affords pentaacetates and periodate oxidation gave the corresponding 1-phenylpyrazole-3-carbaldehyde derivatives, some of which were oxidised to the carboxylic acids.U.v., i.r., and n.m.r. data confirm the proposed structures.
