CAS 4383-22-6

N-benzylprop-2-en-1-amine

Description:

N-benzylprop-2-en-1-amine, also known as benzyl allylamine, is an organic compound characterized by its structure, which features a benzyl group attached to an allylic amine. This compound typically appears as a colorless to pale yellow liquid with a distinct aromatic odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic benzyl group. N-benzylprop-2-en-1-amine is known for its reactivity, particularly in nucleophilic addition reactions, making it useful in organic synthesis and as an intermediate in the production of various pharmaceuticals and agrochemicals. The presence of both an amine and an alkene functional group allows for diverse chemical transformations, including polymerization and coupling reactions. Safety considerations should be taken into account when handling this compound, as it may cause irritation to the skin and eyes. Proper storage in a cool, dry place, away from light and incompatible materials, is recommended to maintain its stability and integrity.

Formula: C₁₀H₁₃N

InChI: InChI=1/C10H13N/c1-2-8-11-9-10-6-4-3-5-7-10/h2-7,11H,1,8-9H2

SMILES: C=CCNCc1ccccc1

Synonyms:

• Benzenemethanamine, N-2-propen-1-yl-
• N-Allylbenzylamine
• N-Benzylprop-2-en-1-amine

N-Allylbenzylamine

CAS: 4383-22-6

Formula: C₁₀H₁₃N

Purity: >97.0%(GC)

Color and Shape: Colorless to Light orange to Yellow clear liquid

Molecular weight: 147.22

Ref: 3B-A2142

N-Benzylprop-2-en-1-amine

CAS: 4383-22-6

Formula: C₁₀H₁₃N

Purity: 97%

Color and Shape: Liquid

Molecular weight: 147.2169

Ref: IN-DA003SPN

N-Benzylprop-2-en-1-amine

CAS: 4383-22-6

N-Benzylprop-2-en-1-amine

Purity: 98%

Color and Shape: Liquid

Molecular weight: 147.22g/mol

Ref: 54-OR906976

N-Allylbenzylamine

CAS: 4383-22-6

Formula: C₁₀H₁₃N

Purity: 97%(stabilized with MEHQ)

Color and Shape: Liquid, Clear

Molecular weight: 147.221

Ref: 10-F036658

N-Allylbenzylamine

CAS: 4383-22-6

N-Allylbenzylamine is an aliphatic hydrocarbon that is found in a variety of natural sources, including peanuts. It has shown anticancer activity against certain cell lines and may be useful in the treatment of cancer. N-Allylbenzylamine reacts with primary amines to form reaction products such as benzyl amine, which is used as a polymerization initiator in the production of polyurethane. The β-amino acid group can be incorporated into proteins by substitution with an amino acid side chain and is important for bone metabolism. N-Allylbenzylamine has also been shown to have anti-inflammatory properties due to its ability to inhibit prostaglandin synthesis.

Formula: C₁₀H₁₃N

Purity: Min. 95%

Molecular weight: 147.22 g/mol

Ref: 3D-EAA38322