2-(Benzylamino)but-3-en-1-ol

Base Information

Chemical Name:2-(Benzylamino)but-3-en-1-ol
CAS No.:50838-63-6
Molecular Formula:C₁₁H₁₅NO
Molecular Weight:177.246
Hs Code.:
DSSTox Substance ID:DTXSID80551580
Nikkaji Number:J1.685.007A
Mol file:50838-63-6.mol

Synonyms:2-(Benzylamino)but-3-en-1-ol;50838-63-6;DTXSID80551580

Suppliers and Price of 2-(Benzylamino)but-3-en-1-ol

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2-(Benzylamino)but-3-en-1-ol

Chemical Property:

XLogP3:1.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:177.115364102
Heavy Atom Count:13
Complexity:141

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C=CC(CO)NCC1=CC=CC=C1

Technology Process of 2-(Benzylamino)but-3-en-1-ol

There total 5 articles about 2-(Benzylamino)but-3-en-1-ol 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: 93.0%

: 119768-88-6
N-benzoyl vinyl glycine methyl ester

: 50838-63-6,53214-59-8
2-Benzylamino-3-buten-1-ol

Guidance literature:: With lithium aluminium tetrahydride; In diethyl ether; for 14h; Heating;
DOI:10.1016/0040-4039(94)88505-2

Reference yield: 65.0%

: 50297-21-7
oxazolidinone

: 50838-63-6,53214-59-8
2-Benzylamino-3-buten-1-ol

Guidance literature:: With potassium hydroxide; tert-butyl alcohol; In water;
DOI:10.1016/S0040-4039(00)96257-9

Reference yield:

: 98-88-4
benzoyl chloride

: 50838-63-6,53214-59-8
2-Benzylamino-3-buten-1-ol

Guidance literature:: Multi-step reaction with 2 steps

1: 50 percent / NaHCO₃ / H₂O; CH₂Cl₂ / 0.5 h / Ambient temperature

2: 93 percent / LiAlH₄ / diethyl ether / 14 h / Heating

With lithium aluminium tetrahydride; sodium hydrogencarbonate; In diethyl ether; dichloromethane; water;
DOI:10.1016/0040-4039(94)88505-2