N-Acetyl-dl-leucine

Name: N-Acetyl-dl-leucine
SKU: ACM99150
Rating: 5 (1 reviews)

CAS

99-15-0

Catalog Number

ACM99150

Category

Other Products

Molecular Weight

173.21

Molecular Formula

C₈H₁₅NO₃

COA MSDS SDS Spec Sheet

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What is the molecular formula of N-Acetyl-dl-leucine according to the reference?

The molecular formula of N-Acetyl-dl-leucine is C8H15NO3.

What is the molecular weight of N-Acetyl-dl-leucine?

The molecular weight of N-Acetyl-dl-leucine is 173.21 g/mol.

What is the IUPAC name of N-Acetyl-dl-leucine?

The IUPAC name of N-Acetyl-dl-leucine is 2-acetamido-4-methylpentanoic acid.

What is the InChIKey of N-Acetyl-dl-leucine?

The InChIKey of N-Acetyl-dl-leucine is WXNXCEHXYPACJF-UHFFFAOYSA-N.

What is the Canonical SMILES of N-Acetyl-dl-leucine?

The Canonical SMILES of N-Acetyl-dl-leucine is CC(C)CC(C(=O)O)NC(=O)C.

What is the CAS number for N-Acetyl-dl-leucine?

The CAS number for N-Acetyl-dl-leucine is 99-15-0.

What is the synonyms for N-Acetyl-dl-leucine?

The synonyms for N-Acetyl-dl-leucine include Acetylleucine and Ac-DL-Leu-OH.

What is the primary use of N-Acetyl-dl-leucine?

N-Acetyl-dl-leucine is used for treating vestibular-related imbalance and vertigo.

What is the XLogP3 value of N-Acetyl-dl-leucine?

The XLogP3 value of N-Acetyl-dl-leucine is 0.5.

How many hydrogen bond donors are there in N-Acetyl-dl-leucine?

There are 2 hydrogen bond donors in N-Acetyl-dl-leucine.

Upstream Synthesis Route 1

60-35-5
201230-82-2
590-86-3

99-15-0

Reference: [1] Angewandte Chemie - International Edition in English, 1997, vol. 36, # 13-14, p. 1494 - 1496

Upstream Synthesis Route 2

60-35-5
763-32-6
201230-82-2

99-15-0

Reference: [1] Journal of Organometallic Chemistry, 1985, vol. 279, p. 203 - 214
[2] Tetrahedron Letters, 1982, vol. 23, # 24, p. 2491 - 2494

Downstream Synthesis Route 1

64-17-5
99-15-0

4071-36-7

Reference: [1] Journal of the American Chemical Society, 1950, vol. 72, p. 1626

Downstream Synthesis Route 2

334-88-3
99-15-0

57289-25-5

Reference: [1]Karrer; Escher; Widmer
[Helvetica Chimica Acta, 1926, vol. 9, p. 317]
[2]Smart,N.A. et al.
[Journal of the Chemical Society, 1960, p. 3902 - 3912]
[3]Calmes, Monique; Daunis, Jacques; Jacquier, Robert; Verducci, Jean
[Tetrahedron, 1987, vol. 43, # 10, p. 2285 - 2292]

Downstream Synthesis Route 3

64-17-5
99-15-0

4071-36-7

Reference: [1]Journal of the American Chemical Society,1950,vol. 72,p. 1626

Downstream Synthesis Route 4

99-15-0

61-90-5

Reference: [1]Beller, Matthias; Eckert, Markus; Geissler, Holger; Napierski, Bernd; Rebenstock, Heinz-Peter; Holla, E. Wolfgang
[Chemistry - A European Journal, 1998, vol. 4, # 5, p. 935 - 941]
[2]Michi; Tsuda
[Journal of the Agricultural Chemical Society of Japan, 1957, vol. 21, p. 235,237]

* For details of the synthesis route, please refer to the original source to ensure accuracy.

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