(Z)-Cinnamylamine

Base Information

• Chemical Name: (Z)-Cinnamylamine
• CAS No.: 4226-59-9
• Molecular Formula: C₉H₁₁N
• Molecular Weight: 133.193
• UNII: S16OZ7JDVK
• Nikkaji Number: J531.464J
• Wikidata: Q27288432
• Mol file: 4226-59-9.mol

Synonyms:cis-Cinnamylamine;(Z)-Cinnamylamine;Cinnamylamine, (Z)-;(Z)-3-Phenylprop-2-en-1-amine;(2Z)-3-Phenylprop-2-en-1-amine;UNII-S16OZ7JDVK;S16OZ7JDVK;4226-59-9;2-Propen-1-amine, 3-phenyl-, (2Z)-;(Z)-3-Phenyl-2-propenylamine;SCHEMBL10422962;AKOS005166895;EN300-383768;Q27288432

Chemical Property of (Z)-Cinnamylamine

Chemical Property:

• Boiling Point: 84 - 87 °C (1.8 mmHg)
• PSA: 26.02000
• Density: 0.993±0.06 g/cm3(Predicted)
• LogP: 2.35880
• XLogP3: 1.7
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 133.089149355
• Heavy Atom Count: 10
• Complexity: 101

Purity/Quality:

95% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C=CCN
• Isomeric SMILES: C1=CC=C(C=C1)/C=C\CN

Technology Process of (Z)-Cinnamylamine

There total 50 articles about (Z)-Cinnamylamine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 99.0%

2-[(E)-3-phenylprop-2-enyl]-2,3-dihydro-1H-isoindole-1,3-dione (17480-07-8) → (E)-cinnamylamine (4335-60-8,4360-51-4,4226-59-9)

Guidance literature:

With hydrazine hydrate; In methanol; at 20 ℃;

DOI:10.1016/j.ejmech.2014.01.049

Reference yield: 98.0%

(E)-cinnamyl azide (57294-86-7,76024-91-4,68340-12-5) → (E)-cinnamylamine (4335-60-8,4360-51-4,4226-59-9)

Guidance literature:

With tin(ll) chloride; In methanol; for 0.5h; Ambient temperature;

DOI:10.1016/S0040-4039(00)84275-6

Reference yield: 96.0%

(2E)-3-phenyl-2-propen-1-ol (4407-36-7) → (E)-cinnamylamine (4335-60-8,4360-51-4,4226-59-9)

Guidance literature:

With sodium azide; triphenylphosphine; In dichloromethane; N,N-dimethyl-formamide; at 90 ℃; for 4h;

DOI:10.1080/00397910008087402

upstream raw materials:

2-[(E)-3-phenylprop-2-enyl]-2,3-dihydro-1H-isoindole-1,3-dione

(1E,2E)-cinnamaldehyde oxime

cinnamic nitrile

bromobenzene

Downstream raw materials:

2-((E)-3-Phenyl-allylamino)-ethanethiol

1,1,1,3,3,3-Hexamethyl-2-((E)-styryl)-disilazane

1H-Indole-2-carboxylic acid ((E)-3-phenyl-allyl)-amide

2-(3-phenyl-2-propenyl)-1,3(2H,4H)-isoquinolinedione