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Merck
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文件

162485

Sigma-Aldrich

邻氟苄胺

96%

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About This Item

線性公式:
FC6H4CH2NH2
CAS號碼:
分子量::
125.14
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
eCl@ss:
39040407
PubChem物質ID:
NACRES:
NA.22

化驗

96%

形狀

liquid

折射率

n20/D 1.517 (lit.)

bp

73-75 °C/13 mmHg (lit.)

密度

1.095 g/mL at 25 °C (lit.)

SMILES 字串

NCc1ccccc1F

InChI

1S/C7H8FN/c8-7-4-2-1-3-6(7)5-9/h1-4H,5,9H2

InChI 密鑰

LRFWYBZWRQWZIM-UHFFFAOYSA-N

應用

2-Fluorobenzylamine was used in synthesis of 9-(2-fluorobenzyl)-6-(methylamino)-9H-purine, having anticonvulsant activity. It was also used in synthesis and study of structure-activity relationship of a series of substituted spirohydantoins.

象形圖

Corrosion

訊號詞

Danger

危險聲明

危險分類

Skin Corr. 1B

儲存類別代碼

8A - Combustible corrosive hazardous materials

水污染物質分類(WGK)

WGK 3

閃點(°F)

152.6 °F - closed cup

閃點(°C)

67 °C - closed cup

個人防護裝備

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


分析證明 (COA)

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Martin W Rowbottom et al.
Bioorganic & medicinal chemistry letters, 17(8), 2171-2178 (2007-03-14)
The design, synthesis, and SAR of a series of substituted spirohydantoins are described. Optimization of an in-house screening hit gave compounds that exhibited potent binding affinity and functional activity at MCH-R1.
9-(2-Fluorobenzyl)-6-(methylamino)-9H-purine hydrochloride. Synthesis and anticonvulsant activity.
J L Kelley et al.
Journal of medicinal chemistry, 29(7), 1133-1134 (1986-07-01)

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