2-Hexen-1-ol, 4-amino-5-methyl-, 1-benzoate, (2E,4S)-

Base Information

Chemical Name:2-Hexen-1-ol, 4-amino-5-methyl-, 1-benzoate, (2E,4S)-
CAS No.:789460-88-4
Molecular Formula:C₁₄H₁₉NO₂
Molecular Weight:233.31
Hs Code.:
DSSTox Substance ID:DTXSID901214431

Synonyms:DTXSID901214431;2-Hexen-1-ol, 4-amino-5-methyl-, 1-benzoate, (2E,4S)-;789460-88-4

Suppliers and Price of 2-Hexen-1-ol, 4-amino-5-methyl-, 1-benzoate, (2E,4S)-

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 2-Hexen-1-ol, 4-amino-5-methyl-, 1-benzoate, (2E,4S)-

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:233.141578849
Heavy Atom Count:17
Complexity:255

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)C(C=CCOC(=O)C1=CC=CC=C1)N
Isomeric SMILES:CC(C)[C@@H](/C=C/COC(=O)C1=CC=CC=C1)N

Technology Process of 2-Hexen-1-ol, 4-amino-5-methyl-, 1-benzoate, (2E,4S)-

There total 3 articles about 2-Hexen-1-ol, 4-amino-5-methyl-, 1-benzoate, (2E,4S)- 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:

: 145037-58-7
Benzoic acid (E)-(S)-4-tert-butoxycarbonylamino-5-methyl-hex-2-enyl ester

: 789460-88-4
Benzoic acid (E)-(S)-4-amino-5-methyl-hex-2-enyl ester

Guidance literature:: With hydrogenchloride; In ethyl acetate; for 3h;
DOI:10.1021/jm00101a005

Reference yield:

: 98-88-4
benzoyl chloride

: 789460-88-4
Benzoic acid (E)-(S)-4-amino-5-methyl-hex-2-enyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N / CH₂Cl₂ / 1.5 h

2: HCl / ethyl acetate / 3 h

With hydrogenchloride; triethylamine; In dichloromethane; ethyl acetate;
DOI:10.1021/jm00101a005

Reference yield:

: 104700-44-9
((E)-(S)-4-Hydroxy-1-isopropyl-but-2-enyl)-carbamic acid tert-butyl ester

: 789460-88-4
Benzoic acid (E)-(S)-4-amino-5-methyl-hex-2-enyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N / CH₂Cl₂ / 1.5 h

2: HCl / ethyl acetate / 3 h

With hydrogenchloride; triethylamine; In dichloromethane; ethyl acetate;
DOI:10.1021/jm00101a005