(4-氟苄基)丁基-1-胺

(4-氟苄基)丁基-1-胺 - Names and Identifiers

Name	N-(4-fluorobenzyl)butan-1-amine
Synonyms	AKOS LT-992X0116 CHEMBRDG-BB 9071894 UKRORGSYN-BB BBV-125484 N-(4-FLUOROBENZYL)-1-BUTANAMINE N-(4-FLUOROBENZYL)BUTAN-1-AMINE N-(4-fluorobenzyl)butan-1-amine N-(4-FLUOROPHENYLMETHYL)BUTYLAMINE benzenemethanamine, N-butyl-4-fluoro-
CAS	60509-35-5
InChI	InChI=1/C11H16FN/c1-2-3-8-13-9-10-4-6-11(12)7-5-10/h4-7,13H,2-3,8-9H2,1H3

(4-氟苄基)丁基-1-胺 - Physico-chemical Properties

Molecular Formula	C11H16FN
Molar Mass	181.25
Density	0.98g/cm³
Boling Point	237.6°C at 760 mmHg
Flash Point	97.5°C
Vapor Presure	0.0444mmHg at 25°C
Storage Condition	Room Temprature
Refractive Index	1.488

(4-氟苄基)丁基-1-胺 - Introduction

N-(4-fluorobenzyl)butan-1-amine is an organic compound with the molecular formula C11H16FN and a molecular weight of 181.25g/mol.

Nature:
N-(4-fluorobenzyl)butan-1-amine is a colorless to light yellow liquid with a special ammonia odor. It is soluble in organic solvents such as alcohols and ethers and practically insoluble in water. It is a corrosive compound and should be handled with caution.

Use:
N-(4-fluorobenzyl)butan-1-amine are often used as organic synthesis intermediates for the synthesis of other compounds. It can be used in the fields of drug synthesis, dye synthesis and pesticide synthesis. It can also be used as a metal coordinating ligand.

Preparation Method:
N-(4-fluorobenzyl)butan-1-amine can be synthesized by benzylation and alkylation reactions. First, butyl bromide and benzyl amide are reacted under appropriate conditions to produce N-(4-fluorobenzyl) butylamine, which is then reduced to N-N-(4-fluorobenzyl)butan-1-amine with a reducing agent.

Safety Information:
N-(4-fluorobenzyl)butan-1-amine is corrosive and contact with skin or eyes may cause irritation and burns. Wear appropriate protective gloves and glasses during use. Avoid inhaling its vapor or dust. Pay attention to fire and explosion prevention during storage and handling, and store in a cool and dry place.

Last Update：2024-04-09 21:01:54