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Merck

197556

Sigma-Aldrich

1-(4-羧基苯基)-3-甲基-5-吡唑酮

≥98%

别名:

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

经验公式(希尔记法):
C11H10N2O3
CAS号:
分子量:
218.21
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

≥98%

mp

285 °C (dec.) (lit.)

SMILES 字串

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

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)

InChI 密鑰

CUGBBQWDGCXWNB-UHFFFAOYSA-N

一般說明

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

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Oral

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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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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