N-Boc-2-piperidinecarboxylic acid

CAS

98303-20-9

Catalog Number

ACM98303209

Category

Other Products

Molecular Weight

229.27

Molecular Formula

C₁₁H₁₉NO₄

MSDS COA Spec Sheet

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What is the molecular formula of N-Boc-2-piperidinecarboxylic acid?

The molecular formula of N-Boc-2-piperidinecarboxylic acid is C11H19NO4.

What is the molecular weight of N-Boc-2-piperidinecarboxylic acid?

The molecular weight of N-Boc-2-piperidinecarboxylic acid is 229.27 g/mol.

What are some synonyms of N-Boc-2-piperidinecarboxylic acid?

Some synonyms of N-Boc-2-piperidinecarboxylic acid include 98303-20-9, 1-(tert-butoxycarbonyl)piperidine-2-carboxylic acid, 1-Boc-piperidine-2-carboxylic acid, and N-Boc-DL-pipecolinic acid.

What is the IUPAC name of N-Boc-2-piperidinecarboxylic acid?

The IUPAC name of N-Boc-2-piperidinecarboxylic acid is 1-[(2-methylpropan-2-yl)oxycarbonyl]piperidine-2-carboxylic acid.

What is the InChIKey of N-Boc-2-piperidinecarboxylic acid?

The InChIKey of N-Boc-2-piperidinecarboxylic acid is JQAOHGMPAAWWQO-UHFFFAOYSA-N.

What is the Canonical SMILES representation of N-Boc-2-piperidinecarboxylic acid?

The Canonical SMILES representation of N-Boc-2-piperidinecarboxylic acid is CC(C)(C)OC(=O)N1CCCCC1C(=O)O.

How many hydrogen bond acceptors does N-Boc-2-piperidinecarboxylic acid have?

N-Boc-2-piperidinecarboxylic acid has 4 hydrogen bond acceptors.

What is the topological polar surface area of N-Boc-2-piperidinecarboxylic acid?

The topological polar surface area of N-Boc-2-piperidinecarboxylic acid is 66.8 Å².

Does N-Boc-2-piperidinecarboxylic acid have any defined atom stereocenters?

No, N-Boc-2-piperidinecarboxylic acid does not have any defined atom stereocenters.

Is N-Boc-2-piperidinecarboxylic acid considered as a canonicalized compound?

Yes, N-Boc-2-piperidinecarboxylic acid is considered a canonicalized compound.

Upstream Synthesis Route 1

24424-99-5
4043-87-2

98303-20-9

Reference: [1] Tetrahedron Letters, 1996, vol. 37, # 20, p. 3441 - 3444

Downstream Synthesis Route 1

98303-20-9

20845-34-5

Reference: [1] Journal of Medicinal Chemistry, 1992, vol. 35, # 23, p. 4334 - 4343
[2] Patent: US5571832, 1996, A,

Downstream Synthesis Route 2

98303-20-9

15883-20-2

Reference: [1] European Journal of Medicinal Chemistry, 1998, vol. 33, # 1, p. 23 - 31

Downstream Synthesis Route 3

98303-20-9

20845-34-5

Reference: [1]Journal of Medicinal Chemistry,1992,vol. 35,p. 4334 - 4343
[2]Patent: US5571832,1996,A

Downstream Synthesis Route 4

98303-20-9

388077-74-5

Reference: [1]Patent: WO2019/86469,2019,A1 .Location in patent: Page/Page column 29

Downstream Synthesis Route 5

5266-85-3
98303-20-9

205993-79-9

Reference: [1]European Journal of Medicinal Chemistry,2001,vol. 36,p. 265 - 286
[2]European Journal of Medicinal Chemistry,1998,vol. 33,p. 23 - 31

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