(2S)-2--4-methylpentan-1-al

Base Information

Chemical Name:(2S)-2--4-methylpentan-1-al
CAS No.:144345-62-0
Molecular Formula:C₁₇H₂₄N₂O₄
Molecular Weight:320.389
Hs Code.:

(2S)-2-<N-(Benzyloxycarbonyl-(R)-alanyl)amino>-4-methylpentan-1-al

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

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Chemical Property of (2S)-2--4-methylpentan-1-al

Chemical Property:

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Technology Process of (2S)-2--4-methylpentan-1-al

There total 3 articles about (2S)-2--4-methylpentan-1-al 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:

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

: 144345-62-0
(2S)-2--4-methylpentan-1-al

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / dioxane / 12 h / Ambient temperature

2: 1.) (COCl)2, DMSO, 2.) Et₃N / 1.) CH₂Cl₂, -78 deg C, 1 h, 2.) -78 deg C, 15 min

With oxalyl dichloride; dimethyl sulfoxide; triethylamine; In 1,4-dioxane;

Reference yield:

: 26607-51-2
N-benzyloxycarbonyl-D-alanine

: 144345-62-0
(2S)-2--4-methylpentan-1-al

Guidance literature:: Multi-step reaction with 3 steps

1: DCC / dioxane / 12 h / Ambient temperature

2: 88 percent / dioxane / 12 h / Ambient temperature

3: 1.) (COCl)2, DMSO, 2.) Et₃N / 1.) CH₂Cl₂, -78 deg C, 1 h, 2.) -78 deg C, 15 min

With oxalyl dichloride; dimethyl sulfoxide; triethylamine; dicyclohexyl-carbodiimide; In 1,4-dioxane;

Reference yield:

: 177657-04-4
(2S)-2-[N-(Benzyloxycarbonyl-(R)-alanyl)amino]-4-methylpentan-1-ol

: 144345-62-0
(2S)-2--4-methylpentan-1-al

Guidance literature:: With oxalyl dichloride; dimethyl sulfoxide; triethylamine; Yield given. Multistep reaction; 1.) CH₂Cl₂, -78 deg C, 1 h, 2.) -78 deg C, 15 min;