2393-23-9

  • Product Name4-Methoxybenzylamine
  • Molecular FormulaC8H11NO
  • Molecular Weight137.181
  • Purity99%
  • Appearanceclear colorless to slightly yellow liquid
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Product Details

Quick Details

  • CasNo: 2393-23-9
  • Molecular Formula: C8H11NO
  • Appearance: clear colorless to slightly yellow liquid
  • Purity: 99%

4-Methoxybenzylamine Good Supplier In Bulk Supply High Purity 2393-23-9

  • Molecular Formula:C8H11NO
  • Molecular Weight:137.181
  • Appearance/Colour:clear colorless to slightly yellow liquid 
  • Vapor Pressure:0.0472mmHg at 25°C 
  • Melting Point:-10 °C 
  • Refractive Index:n20/D 1.546(lit.)  
  • Boiling Point:236.499 °C at 760 mmHg 
  • PKA:9.30±0.10(Predicted) 
  • Flash Point:98.8 °C 
  • PSA:35.25000 
  • Density:1.028 g/cm3 
  • LogP:1.85420 

4-Methoxybenzylamine(Cas 2393-23-9) Usage

Definition

ChEBI: 1-(4-methoxyphenyl)methanamine is an aralkylamino compound that is benzylamine substituted by a methoxy group at the para position. It is a primary amino compound, an aromatic ether and an aralkylamino compound.

Flammability and Explosibility

Notclassified

InChI:InChI=1/C8H11NO/c1-10-8-4-2-7(6-9)3-5-8/h2-5H,6,9H2,1H3/p+1

2393-23-9 Relevant articles

Zirconium-hydride-catalyzed site-selective hydroboration of amides for the synthesis of amines: Mechanism, scope, and application

Han, Bo,Jiao, Haijun,Wu, Lipeng,Zhang, Jiong

, p. 2059 - 2067 (2021/09/02)

Developing mild and efficient catalytic ...

Deoxygenative hydroboration of primary, secondary, and tertiary amides: Catalyst-free synthesis of various substituted amines

An, Duk Keun,Jaladi, Ashok Kumar,Kim, Hyun Tae,Yi, Jaeeun

, (2021/11/17)

Transformation of relatively less reacti...

Method for preparing primary amine by catalytically reducing nitrile compounds through nano-porous palladium catalyst

-

Paragraph 0073-0076, (2021/05/29)

The invention belongs to the technical f...

Cobalt-Catalyzed Hydrogenative Transformation of Nitriles

Zhang, Shaoke,Duan, Ya-Nan,Qian, Yu,Tang, Wenyue,Zhang, Runtong,Wen, Jialin,Zhang, Xumu

, p. 13761 - 13767 (2021/11/17)

Here, we report the transformation of ni...

2393-23-9 Process route

benzyl-(4-methoxybenzyl)amine
14429-02-8

benzyl-(4-methoxybenzyl)amine

benzaldehyde
100-52-7

benzaldehyde

4-methoxy-benzaldehyde
123-11-5

4-methoxy-benzaldehyde

4-methoxy-benzylamine
2393-23-9

4-methoxy-benzylamine

benzylamine
100-46-9

benzylamine

Conditions
Conditions Yield
With dihydrogen peroxide; sodium phosphate; horseradish peroxidase; In methanol; water; at 37 ℃; for 0.5h; pH=7.4; Further Variations:; Reaction partners; Kinetics;
sulfuric acid
7664-93-9

sulfuric acid

N-(4-methoxybenzyl)benzaldimine
31490-38-7

N-(4-methoxybenzyl)benzaldimine

benzaldehyde
100-52-7

benzaldehyde

4-methoxy-benzylamine
2393-23-9

4-methoxy-benzylamine

Conditions
Conditions Yield

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