What is the 4-Methoxybenzylamine?

4-Methoxybenzylamine is clear colorless to slightly yellow liquid, while it's Molecular Formula is C8H11NO. clear colorless to slightly yellow liquid 4-Methoxybenzylamine is an important raw material and intermediate used in Organic Synthesis, Pharmaceuticals, Agrochemicals and Dyestuff. It is also used fine chemical intemediate.

What is the CAS number for 4-Methoxybenzylamine?

The CAS number of 4-Methoxybenzylamine is 2393-23-9.

What is the 4-Methoxybenzylamine?

4-Methoxybenzylamine is clear colorless to slightly yellow liquid, while it's Molecular Formula is C8H11NO. clear colorless to slightly yellow liquid 4-Methoxybenzylamine is an important raw material and intermediate used in Organic Synthesis, Pharmaceuticals, Agrochemicals and Dyestuff. It is also used fine chemical intemediate.

What is the CAS number for 4-Methoxybenzylamine?

The CAS number of 4-Methoxybenzylamine is 2393-23-9.

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

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

: 100-52-7
benzaldehyde

: 123-11-5
4-methoxy-benzaldehyde

: 2393-23-9
4-methoxy-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;