N-Boc-piperidin-4-ylpropionic acid

N-Boc-piperidin-4-ylpropionic acid - Names and Identifiers

Name	1-BOC-PIPERIDIN-4-YLPROPIONIC ACID
Synonyms	Boc-piperidine-4-propanoic acid 1-Boc-4-piperidinepropanoic acid 1-BOC-PIPERIDINE-4-PROPANOIC ACID 1-BOC-PIPERIDIN-4-YLPROPIONIC ACID N-Boc-piperidin-4-ylpropionic acid N-BOC-PIPERIDINYL-4-PROPIONIC ACID 3-(1-tert-Butoxycarbonyl-4-piperidyl)propanoic acid 3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propanoic acid 4-Piperidinepropanoic acid, 1-[(1,1-dimethylethoxy)carbonyl]-
CAS	154775-43-6

N-Boc-piperidin-4-ylpropionic acid - Physico-chemical Properties

Molecular Formula	C13H23NO4
Molar Mass	257.33
Density	1.102±0.06 g/cm3(Predicted)
Boling Point	386.4±15.0 °C(Predicted)
pKa	4.73±0.10(Predicted)
Storage Condition	2-8°C

N-Boc-piperidin-4-ylpropionic acid - Risk and Safety

Hazard Symbols	Xn - Harmful
Risk Codes	22 - Harmful if swallowed
HS Code	29333990

N-Boc-piperidin-4-ylpropionic acid - Upstream Downstream Industry

Raw Materials

(E)-tert-Butyl 4-(3-methoxy-3-oxoprop-1-en-1-yl)piperidine-1-carboxylate
1-Piperidinecarboxylic acid, 4-(2-carboxyethylidene)-, 1-(1,1-dimethylethyl) ester
METHYL N-BOC-4-PIPERIDINEPROPIONATE
3-PIPERIDIN-4-YL-PROPIONIC ACID
tert-butyl 4-(3-ethoxy-3-oxopropyl)piperidine-1-carboxylate
3-(4-Pyridine)acrylic acid
4-Piperidinepropanoic acid, hydrochloride
1-Boc-4-[methoxy(methyl)carbamoyl]piperidine
1-tert-Butoxycarbonyl-4-piperidinecarboxaldehyde
N-BOC-piperidine-4-carboxylic acid
Di-tert-butyl dicarbonate
Isonipecotic acid

N-Boc-piperidin-4-ylpropionic acid - Introduction

ACID is an organic compound with the molecular formula C14H23NO4, and the structure contains a BOC (hydroxymethylpropionyl) protecting group.

ACID is often used as an intermediate in organic synthesis, especially in the field of medicine. It can be used to prepare a variety of drugs and bioactive molecules, such as anti-cancer drugs, nerve conduction regulators, etc.

The method for preparing the phosphonic ACID is generally obtained by reacting piperidine and N-Boc propionimide. Specific synthesis steps: first propionyl chloride reaction to get N-propionyl piperidine, and then through the reaction with Boc2O, add base, get ACID.

Regarding safety information, ACID is generally not significantly toxic to humans, but as an organic compound, attention should be paid to its safe operation in laboratories and industrial production. It may cause irritation to the eyes, skin and respiratory tract, so wear appropriate protective equipment when handling, avoid contact with skin and eyes, and ensure adequate ventilation.

Last Update：2024-04-09 20:49:11