Leucine, 2-(2-methylpropyl)-

Base Information

• Chemical Name: Leucine, 2-(2-methylpropyl)-
• CAS No.: 99863-59-9
• Molecular Formula: C10H21NO2
• Molecular Weight: 187.27900
• DSSTox Substance ID: DTXSID80476380
• Nikkaji Number: J1.908.883I

Synonyms:Leucine, 2-(2-methylpropyl)-;99863-59-9;2-Amino-2-isobutyl-4-methylpentanoic acid;2-Isobutyl-DL-leucine;starbld0042955;SCHEMBL497762;2-AMINO-4-METHYL-2-(2-METHYLPROPYL)PENTANOIC ACID;DTXSID80476380;NHHUZNBRAXROKE-UHFFFAOYSA-N;MFCD02662639;2-amino-2-isobutyl-4-methylvaleric acid;SY265407;CS-0457850

Chemical Property of Leucine, 2-(2-methylpropyl)-

Chemical Property:

• Boiling Point: 282.8±23.0 °C(Predicted)
• PSA: 63.32000
• Density: 0.971±0.06 g/cm3(Predicted)
• LogP: 2.56100
• XLogP3: -0.2
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 5
• Exact Mass: 187.157228913
• Heavy Atom Count: 13
• Complexity: 166

Purity/Quality:

99% ^*data from raw suppliers

Leucine,2-(2-methylpropyl)- ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)CC(CC(C)C)(C(=O)O)N

Technology Process of Leucine, 2-(2-methylpropyl)-

There total 4 articles about Leucine, 2-(2-methylpropyl)- 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: 91.0%

ethyl 2,2-bis(allyl)-2-nitroacetate (93823-12-2) → 2,2-diisobutylglycine (99863-59-9)

Guidance literature:

With potassium hydroxide; In ethanol; for 24h; Heating;

DOI:10.1021/jo034885j

Reference yield:

2,2-diisobutyl-malonamic acid (854851-20-0) → 2,2-diisobutylglycine (99863-59-9)

Guidance literature:

With alkaline NaOBr; at -10 - -5 ℃;

Reference yield:

5,5-diisobutyl-imidazolidine-2,4-dione (36033-48-4) → 2,2-diisobutylglycine (99863-59-9)

Guidance literature:

(hydrolysis);

DOI:10.1021/jm00273a004

upstream raw materials:

2,2-diisobutyl-malonamic acid

5,5-diisobutyl-imidazolidine-2,4-dione

ethyl 2,2-bis(allyl)-2-nitroacetate

Downstream raw materials:

N^α-(benzyloxycarbonyl)-2,2-diisobutylglycine

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