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510297

Sigma-Aldrich

5-溴-2-甲氧基吡啶

95%

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About This Item

经验公式（希尔记法）:
C6H6BrNO
CAS号:
13472-85-0
分子量:
188.02
MDL號碼:
MFCD01318952
分類程式碼代碼:
12352100
PubChem物質ID:
24873491
NACRES:
NA.22

化驗

95%

折射率

n20/D 1.555 (lit.)

bp

80 °C/12 mmHg (lit.)

密度

1.453 g/mL at 25 °C (lit.)

官能基

bromo

SMILES 字串

COc1ccc(Br)cn1

InChI

1S/C6H6BrNO/c1-9-6-3-2-5(7)4-8-6/h2-4H,1H3

InChI 密鑰

XADICJHFELMBGX-UHFFFAOYSA-N

應用

αvβ3 拮抗剂的 β-丙氨酸部分的结构单元也是合成强效选择性促生长素抑制素 sst3 受体拮抗剂的结构单元。

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）

204.8 °F - closed cup

閃點（°C）

96 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
0000109592
0000053279
BGBC5322V
0000052339
BGBB5744V

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Sigma-Aldrich

683345

[Pd2(dba)3] x dba

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The Journal of organic chemistry, 69(6), 1959-1966 (2004-04-03)
A practical preparation of an alpha(v)beta(3) antagonist is reported. The antagonist consists of three key components, a tetrahydronaphthyridine moiety, a beta-alanine moiety, and a central imidazolidone moiety. The tetrahydronaphthyridine component was prepared using two different methods, both of which relied
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A scaleable synthesis of methyl 3-amino-5-(4-fluorobenzyl)-2-pyridinecarboxylate.
Organic Process Research & Development 11.5 (2007): 899-902
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A series of 3-substituted tetrahydro-[1,8]naphthyridine containing alpha(v)beta(3) antagonists was prepared. A comparison of their in vitro IC(50) values to the electron properties of the 3-substituents revealed a good linear Hammett correlation (rho=-1.96, R(2)=0.959). Electron-withdrawing groups at the 3-position of the
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