3-(2-Hydroxyethyl)piperidine-1-carboxylic acid tert-butyl ester

• CAS: 146667-84-7
• Catalog Number: ACM146667847
• Category: Other Products
• Molecular Weight: 229.32
• Molecular Formula: C₁₂H₂₃NO₃
• Synonyms: 3-(2-HYDROXY-ETHYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER;1-N-BOC-PIPERIDINE-3-ETHANOL;1-BOC-3-(2-HYDROXY-ETHYL)-PIPERIDINE;TERT-BUTYL 3-(2-HYDROXYETHYL)PIPERIDINE-1-CARBOXYLATE;1-Boc-piperidine-3-ethanol;1-Boc-3-hydroxyethyl piperidine;1-N-Boc-piperidine-3-ethanol ,98%;N-Boc-3-(2-hydroxyethyl)piperidine

Custom Q&A

What is the molecular formula of 3-(2-Hydroxyethyl)piperidine-1-carboxylic acid tert-butyl ester?

The molecular formula is C12H23NO3.

What is the molecular weight of 3-(2-Hydroxyethyl)piperidine-1-carboxylic acid tert-butyl ester?

The molecular weight is 229.32 g/mol.

What is the IUPAC name of 3-(2-Hydroxyethyl)piperidine-1-carboxylic acid tert-butyl ester?

The IUPAC name is tert-butyl 3-(2-hydroxyethyl)piperidine-1-carboxylate.

What is the InChI key of 3-(2-Hydroxyethyl)piperidine-1-carboxylic acid tert-butyl ester?

The InChI key is DXABICKZWDHPIP-UHFFFAOYSA-N.

How many hydrogen bond donor counts are there in 3-(2-Hydroxyethyl)piperidine-1-carboxylic acid tert-butyl ester?

There is 1 hydrogen bond donor count.

What is the hydrogen bond acceptor count in 3-(2-Hydroxyethyl)piperidine-1-carboxylic acid tert-butyl ester?

There are 3 hydrogen bond acceptor counts.

What is the topological polar surface area of 3-(2-Hydroxyethyl)piperidine-1-carboxylic acid tert-butyl ester?

The topological polar surface area is 49.8 Ų.

How many rotatable bond counts are present in 3-(2-Hydroxyethyl)piperidine-1-carboxylic acid tert-butyl ester?

There are 4 rotatable bond counts.

Is 3-(2-Hydroxyethyl)piperidine-1-carboxylic acid tert-butyl ester a canonicalized compound?

Yes, the compound is canonicalized.

What is the CAS number of 3-(2-Hydroxyethyl)piperidine-1-carboxylic acid tert-butyl ester?

The CAS number is 146667-84-7.

Synthetic Use

Upstream Synthesis Route 1

• 146667-83-6

• 146667-84-7

Reference: [1] Journal of Heterocyclic Chemistry, 1992, vol. 29, # 6, p. 1663 - 1665

Upstream Synthesis Route 2

• 73579-06-3
• 24424-99-5

• 146667-84-7

Reference: [1] Bioorganic and medicinal chemistry letters, 2002, vol. 12, # 13, p. 1785 - 1789

Upstream Synthesis Route 3

• 6293-56-7

• 146667-84-7

Reference: [1] Journal of Heterocyclic Chemistry, 1992, vol. 29, # 6, p. 1663 - 1665

Upstream Synthesis Route 4

• 146667-83-6

• 146667-84-7

Reference: [1]Journal of Heterocyclic Chemistry,1992,vol. 29,p. 1663 - 1665

Upstream Synthesis Route 5

• 73579-06-3
• 24424-99-5

• 146667-84-7

Reference: [1]Bioorganic and medicinal chemistry letters,2002,vol. 12,p. 1785 - 1789

Downstream Synthesis Route 1

• 98-59-9
• 146667-84-7

• 146667-85-8

Reference: [1]Journal of Heterocyclic Chemistry,1992,vol. 29,p. 1663 - 1665

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