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126896

间氟苄胺

Name: 间氟苄胺
Brand: ALDRICH

97%

别名:

(3-Fluorophenyl)methanamine, 1-(3-Fluorophenyl)methanamine, 3-Fluorobenzenemethanamine, 3-Fluorophenylmethylamine, m-Fluorobenzylamine

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关于此项目

线性分子式:

FC₆H₄CH₂NH₂

化学文摘社编号:

100-82-3

分子量:

125.14

PubChem Substance ID:

24847749

eCl@ss:

39040408

UNSPSC Code:

12352100

NACRES:

NA.22

EC Number:

202-891-3

MDL number:

MFCD00008113

Assay:

97%

Form:

liquid

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属性

Quality Level

100

assay

97%

form

liquid

refractive index

n20/D 1.514 (lit.)

density

1.097 g/mL at 25 °C (lit.)

functional group

amine, fluoro

SMILES string

NCc1cccc(F)c1

InChI

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

InChI key

QVSVMNXRLWSNGS-UHFFFAOYSA-N

说明

Application

3-Fluorobenzylamine has been used to study the rate of reaction of benzylamines with 1-Chloro-2,4-dinitrobenzene and toluene-p-sulphonyl chloride. It has also been used in the synthesis of substituted amino-sulfonamide protease inhibitors (PIs) DPC 681 and DPC 684.

pictograms

GHS05

signalword

Danger

hcodes

H314

pcodes

P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363 - P405

Hazard Classifications

Skin Corr. 1B

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

159.8 °F - closed cup

flash_point_c

71 °C - closed cup

ppe

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

0000428357

0000173812

MKCS2350

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Fischer A, et al.

Journal of the Chemical Society B: Physical Organic, 466-468 (1966)

Physical properties, ligand substitution reactions, and biological activity of Co(iii)-Schiff base complexes.

A Paden King et al.

Dalton transactions (Cambridge, England : 2003), 48(18), 5987-6002 (2019-01-24)

Four cobalt(iii) complexes of the general formula [Co(Schiff base)(L)2]+, where L is ammonia (NH3) or 3-fluorobenzylamine (3F-BnNH2), were synthesized. The complexes were characterized by NMR spectroscopy, mass spectrometry, and X-ray crystallography. Their electrochemical properties, ligand substitution mechanisms, and ligand exchange

Design, synthesis and evaluation of coumarin-pargyline hybrids as novel dual inhibitors of monoamine oxidases and amyloid-β aggregation for the treatment of Alzheimer's disease.

Hua-Li Yang et al.

European journal of medicinal chemistry, 138, 715-728 (2017-07-21)

A series of coumarin-pargyline hybrids (4a-x) have been designed, synthesized and evaluated as novel dual inhibitors of Alzheimer's disease (AD). Most of the compounds exhibited a potent ability to inhibit amyloid-β (Aβ) aggregation and monoamine oxidases. In particular, compound 4x

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全球贸易项目编号

货号	GTIN
126896-5G	04061838724489
126896-1G	04061837506147