3910-58-5

Basic information

• Product Name: CHEMBRDG-BB 4022333
• Synonyms: UKRORGSYN-BB BBV-125487;N-(4-methoxybenzyl)butan-1-amine(SALTDATA: FREE);N-Butyl-4-Methoxy-benzeneMethanaMine;N-Butyl-p-Methoxy-benzylaMine;N-n-Butyl-4-MethoxybenzylaMine, 97%;CHEMBRDG-BB 4022333;N-(4-Methoxybenzyl)-1-butanamine;N-(4-METHOXYBENZYL)BUTAN-1-AMINE
• CAS NO: 3910-58-5
• Molecular Formula: C₁₂H₁₉NO
• Molecular Weight: 193.288
• Mol File: 3910-58-5.mol
• Article Data: 18

Chemical Properties

• Boiling Point: 277.6°C at 760 mmHg
• Flash Point: 115°C
• Appearance: /
• Density: 0.944g/cm³
• Vapor Pressure: 0.00449mmHg at 25°C
• Refractive Index: 1.498
• Storage Temp.: Refrigerator
• Solubility: Chloroform, Methanol
• CAS DataBase Reference: CHEMBRDG-BB 4022333(CAS DataBase Reference)
• NIST Chemistry Reference: CHEMBRDG-BB 4022333(3910-58-5)
• EPA Substance Registry System: CHEMBRDG-BB 4022333(3910-58-5)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 3910-58-5(Hazardous Substances Data)

Usage

Uses

Synthetic intermediate. Can be used in the synthesis of dialkylphenanthrenylamines.

InChI:InChI=1/C12H19NO/c1-3-4-9-13-10-11-5-7-12(14-2)8-6-11/h5-8,13H,3-4,9-10H2,1-2H3

Upstream product

• 2746-25-0 p-Methoxybenzyl bromide 
• 109-73-9 N-butylamine 
• 3910-55-2 N-(p-methoxybenzylidene)butylamine 
• 123-11-5 4-methoxy-benzaldehyde 
• 874-90-8 4-methoxybenzonitrile 
• 100-07-2 4-methoxy-benzoyl chloride 
• 2280-99-1 N-butyl-p-methoxybenzamide 
• 7332-00-5 n-butylazide 
• 105-13-5 4-Methoxybenzyl alcohol 
• 3910-55-2 N-(4-methoxybenzylidene)-n-butylamine 
• 6117-91-5 (E/Z)-2-buten-1-ol 
• 2393-23-9 4-methoxy-benzylamine 
• 109-65-9 1-bromo-butane 

Downstream Products

• 24922-69-8 BuNH₂*TFA 
• 123-11-5 4-methoxy-benzaldehyde 
• 2280-99-1 N-butyl-p-methoxybenzamide 
• 1027986-05-5 [(E)-2-(2-Bromo-3,4,5-trimethoxy-phenyl)-1-(4-methoxy-phenyl)-vinyl]-butyl-(4-methoxy-benzyl)-amine 
• 367943-59-7 [[butyl-(4-methoxy-benzyl)-amino]-(4-methoxy-phenyl)-methyl]-phosphonic acid dimethyl ester 

Relevant articles and documents

Polyoxometalate-Driven Ease Conversion of Valuable Furfural to trans- N, N-4,5-Diaminocyclopenten-2-ones

We investigated the catalytic efficacy of silicotungstic acid (H4SiW12O40) polyoxometalate (POM) toward the reaction between furfural and amines that selectively yields trans-N,N-4,5-substituted-diaminocyclopenten-2-ones (trans-DACPs). H4SiW12O40 facilita

Intramolecular C?H Amination of N-Alkylsulfamides by tert-Butyl Hypoiodite or N-Iodosuccinimide

1,3-Diamines are an important class of compounds that are broadly found in natural products and are also widely used as building blocks in organic synthesis. Although the intramolecular C?H amination of N-alkylsulfamide derivatives is a reliable method for the construction of 1,3-diamine structures, the majority of these methods involve the use of a transition-metal catalyst. We herein report on a new transition-metal-free method using tert-butyl hypoiodite (t-BuOI) or N-iodosuccinimide (NIS), enabling secondary non-benzylic and tertiary C?H amination reactions to proceed. The cyclic sulfamide products can be easily transformed into 1,3-diamines. Mechanistic investigations revealed that amination reactions using t-BuOI or NIS each proceed via different pathways.

Photocatalyzed cascade Meerwein addition/cyclization of: N -benzylacrylamides toward azaspirocycles

A visible-light-induced cascade Meerwein addition/cyclization of alkenes involving C-F bond cleavage was developed. This method offers a rapid access to azaspirocyclic cyclohexadienones from N-benzylacrylamides via C-F bond cleavage applying H2O as an external oxygen source, allowing for the incorporation of various aromatic moieties originating from aryldiazonium salts.