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Merck
CN

197556

4-(3-Methyl-5-oxo-2-pyrazolin-1-yl)benzoic acid

≥98%

Synonym(s):

1-(4-Carboxyphenyl)-3-methyl-2-pyrazolin-5-one, 1-(4-Carboxyphenyl)-3-methyl-2-pyrazolinone, 1-(4-Carboxyphenyl)-3-methyl-5-pyrazolone, 1-(p-Carboxyphenyl)-3-methyl-5-pyrazolone, 4-(3-Methyl-5-oxo-4,5-dihydro-1H-pyrazol-1-yl)benzoic acid, 4-(3-Methyl-5-oxopyrazol-1-yl)benzoic acid, 4-(4,5-Dihydro-3-methyl-5-oxo-1H-pyrazol-1-yl)benzoic acid

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About This Item

Empirical Formula (Hill Notation):
C11H10N2O3
CAS Number:
60875-16-3
Molecular Weight:
218.21
NACRES:
NA.22
PubChem Substance ID:
24851835
UNSPSC Code:
12352100
EC Number:
262-509-6
MDL number:
MFCD00003135

Key Documents

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Product Name

4-(3-Methyl-5-oxo-2-pyrazolin-1-yl)benzoic acid, ≥98%

InChI key

CUGBBQWDGCXWNB-UHFFFAOYSA-N

InChI

1S/C11H10N2O3/c1-7-6-10(14)13(12-7)9-4-2-8(3-5-9)11(15)16/h2-5H,6H2,1H3,(H,15,16)

SMILES string

CC1=NN(C(=O)C1)c2ccc(cc2)C(O)=O

assay

≥98%

mp

285 °C (dec.) (lit.)

functional group

carboxylic acid

Quality Level

100

Related Categories

General description

The pharmacological activity of 4-(3-methyl-5-oxo-2-pyrazolin-1-yl)benzoic acid was studied.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
MKCW6312
0000256932
0000256932
0000001503
0000000869

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G M Antón-Fos et al.
Arzneimittel-Forschung, 44(7), 821-826 (1994-07-01)
New compounds showing hypoglycaemic activity have been designed through a computer-aided method based on QSAR (quantitative structure activity relationship) and molecular connectivity. The pharmacological tests carried out on the newly designed compounds demonstrated the existence of notable activity for two
Xixi Chen et al.
EBioMedicine, 25, 143-153 (2017-10-17)
Glycated haemoglobin (HbA1c) is the most important marker of hyperglycaemia in diabetes mellitus. We show that d-ribose reacts with haemoglobin, thus yielding HbA1c. Using mass spectrometry, we detected glycation of haemoglobin with d-ribose produces 10 carboxylmethyllysines (CMLs). The first-order rate

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