Key Documents

View All Documentation

126896

3-Fluorobenzylamine

Name: 3-Fluorobenzylamine
Brand: ALDRICH

97%

Synonym(s):

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

Select a Size

Change View

About This Item

Linear Formula:

FC₆H₄CH₂NH₂

CAS Number:

100-82-3

Molecular Weight:

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

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Properties

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

Description

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

Storage Class

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

0000428357

0000173812

MKCS2350

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Fischer A, et al.

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

DPC 681 and DPC 684: potent, selective inhibitors of human immunodeficiency virus protease active against clinically relevant mutant variants.

R F Kaltenbach et al.

Antimicrobial agents and chemotherapy, 45(11), 3021-3028 (2001-10-16)

Human immunodeficiency virus (HIV) protease inhibitors (PIs) are important components of many highly active antiretroviral therapy regimens. However, development of phenotypic and/or genotypic resistance can occur, including cross-resistance to other PIs. Development of resistance takes place because trough levels of

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

View All Related Papers

Global Trade Item Number

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