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Merck
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文件

548030

Sigma-Aldrich

3-溴-4-甲基吡啶

96%

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About This Item

经验公式（希尔记法）:
C6H6BrN
CAS号:
3430-22-6
分子量:
172.02
MDL號碼:
MFCD00082592
分類程式碼代碼:
12352100
PubChem物質ID:
24879007
NACRES:
NA.22

化驗

96%

折射率

n20/D 1.56 (lit.)

bp

199-200 °C (lit.)

密度

1.549 g/mL at 25 °C (lit.)

SMILES 字串

Cc1ccncc1Br

InChI

1S/C6H6BrN/c1-5-2-3-8-4-6(5)7/h2-4H,1H3

InChI 密鑰

GSQZOLXWFQQJHJ-UHFFFAOYSA-N

應用

3-Bromo-4-methylpyridine may be used as a building block in the preparation of:
  • substituted 4-(2,2-diphenylethyl)pyridine-N-oxides for use as potent phosphodiesterase type 4 (PDE4) inhibitors
  • benzodiazepine site ligands bearing tricyclic pyridone moiety for human GABAA receptor
  • a novel isomer of ascididemin
  • 3-bromopyridine-4-carbonitrile

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險聲明

H315,H319,H335

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

10 - Combustible liquids

水污染物質分類（WGK）

WGK 3

閃點（°F）

174.9 °F - closed cup

閃點（°C）

79.4 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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James Crawforth et al.
Bioorganic & medicinal chemistry letters, 14(7), 1679-1682 (2004-03-18)
A series of tricyclic pyridones has been evaluated as benzodiazepine site ligands with functional selectivity for the alpha(3) over the alpha(1) containing subtype of the human GABA(A) receptor ion channel. This investigation led to the identification of a high affinity
Richard Frenette et al.
Bioorganic & medicinal chemistry letters, 12(20), 3009-3013 (2002-09-25)
A detailed SAR study directed toward the optimization of pharmacokinetic parameters for analogues of L-791,943 is reported. The introduction of a soft metabolic site on this structure permitted the identification of L-826,141 as a potent phosphodiesterase type 4 (PDE4) inhibitor
Condensed heteroaromatic ring systems. XV. Synthesis of pyranopyridinones from halopyridinecarbonitriles.
Sakamoto T, et al.
Chemical & Pharmaceutical Bulletin, 36(5), 1890-1894 (1988)
Ida Nymann Petersen et al.
Chemical communications (Cambridge, England), 48(72), 9092-9094 (2012-08-07)
A new and convergent synthesis of ascididemin is presented. Using an anionic cascade ring closure as the key step, this natural product is obtained in 45% overall yield in just 6 steps starting from 2'-fluoroacetophenone. This new approach was extended

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