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Merck

278246

Sigma-Aldrich

3-氰基-6-甲基-2(1H)-吡啶酮

97%

别名:

1,2-二氢-6-甲基-2-氧代-3-氰基吡啶

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About This Item

经验公式(希尔记法):
C7H6N2O
CAS号:
分子量:
134.14
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

97%

mp

293-295 °C (lit.)

SMILES 字串

CC1=CC=C(C#N)C(=O)N1

InChI

1S/C7H6N2O/c1-5-2-3-6(4-8)7(10)9-5/h2-3H,1H3,(H,9,10)

InChI 密鑰

FIMGYEKEYXUTGD-UHFFFAOYSA-N

一般說明

Supramolecular structures of coordination copper(I) compounds of 3-cyano-6-methyl-2(1H)-pyridinone has been investigated.

應用

3-Cyano-6-methyl-2(1H)-pyridinone has been used in the preparation of the N3′-pyridyl thiamine, a potent in vitro thiamine antagonist.

象形圖

Exclamation mark

訊號詞

Warning

危險分類

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

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

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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Allen A Thomas et al.
Bioorganic & medicinal chemistry letters, 18(6), 2206-2210 (2008-02-13)
Tumor cells extensively utilize the pentose phosphate pathway for the synthesis of ribose. Transketolase is a key enzyme in this pathway and has been suggested as a target for inhibition in the treatment of cancer. In a pharmacodynamic study, nude
Construction of three-dimensional supramolecular coordination copper (I) compounds with channel structures hosting a variety of anions by changing the hydrogen-bonding mode and distances.
Munakata M, et al.
Journal of the American Chemical Society, 118(13), 3117-3124 (1996)

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