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N-Boc-3-carboethoxy-4-piperidone

N-Boc-3-carboethoxy-4-piperidone Structure
CAS No.
98977-34-5
Chemical Name:
N-Boc-3-carboethoxy-4-piperidone
Synonyms
1-tert-butyl 3-ethyl 4-oxopiperidine-1,3-dicarboxylate;N-Boc-4-Oxo-3-piperidinecarboxylic acid ethyl ester;N-Boc-3-carboethoxy piperidone;4-oxopiperidine-1,3-dicarboxyL;N-Boc-3-Carboethxy-4-Piperidone;N-BOC-3-CARBETHOXY-4-PIPERIDONE;N-BOC-3-CARBOETHOXY-4-PIPERIDONE;N-T-BOC-3-CARBOETHOXY-4-PIPERIDONE;N-BOC-3-CARBOETHOXY-4-PIPERIDONE-C;1-Boc-3-ethoxycarbonyl-4-piperidone
CBNumber:
CB5762671
Molecular Formula:
C13H21NO5
Molecular Weight:
271.31
MOL File:
98977-34-5.mol
Modify Date:
2024/7/22 11:03:48

N-Boc-3-carboethoxy-4-piperidone Properties

Melting point 62.0 to 66.0 °C
Boiling point 364.6±42.0 °C(Predicted)
Density 1.152±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form powder to crystal
pka 11.08±0.20(Predicted)
color White to Yellow

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
Risk Statements  36/38
Safety Statements  36
HS Code  29333990

N-Boc-3-carboethoxy-4-piperidone price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemicals (India) E0983 Ethyl 1-tert-Butoxycarbonyl-4-oxo-3-piperidinecarboxylate 98977-34-5 1G ₹3500 2022-05-26 Buy
TCI Chemicals (India) E0983 Ethyl 1-tert-Butoxycarbonyl-4-oxo-3-piperidinecarboxylate 98977-34-5 5G ₹7600 2022-05-26 Buy
Product number Packaging Price Buy
E0983 1G ₹3500 Buy
E0983 5G ₹7600 Buy

N-Boc-3-carboethoxy-4-piperidone Chemical Properties,Uses,Production

Description

N-Boc-3-Carboethoxy-4-piperidone has several applications in scientific research. It is used as a biochemical reagent, a pharmaceutical intermediate, and a building block in organic synthesis. In biochemical research, N-Boc-3-Carboethoxy-4-piperidone can be a substrate for various enzymes, such as proteases and glycosidases. It can also be used as a starting material for synthesising various pharmaceuticals, such as antibiotics and anti-inflammatory drugs. Finally, it can be used as a building block in organic synthesis, as it can be used to synthesize various polymers and other organic compounds.

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N-Boc-3-carboethoxy-4-piperidone Spectrum

Ethyl N-Boc-4-oxopiperidine-3-carboxylate N-Boc-3-carboethoxy piperidone Ethyl 1-tert-Butoxycarbonyl-4-oxo-3-piperidinecarboxylate N-Boc-3-Carboethxy-4-Piperidone 1,3-Piperidinedicarboxylic acid, 4-oxo-, 1-(1,1-diMethylethyl) 3-ethyl ester 1-Tert-butoxycarbonyl-4-oxo-3-piperidinecarboxylate ethyl ester/N-Boc-3-carboethoxy-4-piperidone 1-tert-Butoxycarbonyl-3-(ethoxycarbonyl)piperidin-4-one Ethyl 1-tert-Butoxycarbonyl-4-oxo-3-piperidinecarboxylate Ethyl 1-Boc-4-piperidone-3-carboxylate 4-OXO-PIPERIDINE-1,3-DICARBOXYLIC ACID 1-TERT-BUTYL ESTER 3-ETHYL ESTER 1-N-BOC-4-OXO-3-PIPERIDINECARBOXYLIC ACID ETHYL ESTER N-BOC-3-CARBETHOXY-4-PIPERIDONE N-BOC-3-CARBOETHOXY-4-PIPERIDONE N-T-BOC-3-CARBOETHOXY-4-PIPERIDONE 1-Boc-4-oxo-3-piperidine carboxylic acid ethyl ester Ethyl 1-(tert-butoxycarbonyl)-4-oxopiperidine-3-carboxylate, 1-tert-Butyl 3-ethyl 4-oxopiperidine-1,3-dicarboxylate Ethyl 4-oxopiperidine-3-carboxylate, N-BOC protected Ethyl-N-Boc-4-piperidone-3-carboxylate 1-O-tert-butyl 3-O-ethyl 4-oxopiperidine-1,3-dicarboxylate N-BOC-3-CARBOETHOXY-4-PIPERIDONE-C 4-Oxo-piperidine-1,3-dicarboxylic acid Ethyl 1-n-boc-4-oxo-3-piperidine carboxylate Ethyl1-tert-Butoxycarbonyl-4-oxo-3-piperidinecarboxylate> 4-oxopiperidine-1,3-dicarboxyL 1-tert-Butoxycarbonyl-3-ethoxycarbonyl-4-piperidone 1-Boc-3-ethoxycarbonyl-4-piperidone Ethyl 1-Boc-4-oxo-3-piperidinecarboxylate 1-tert-Butoxycarbonyl-4-oxo-3-piperidinecarboxylic Acid Ethyl Ester 1-tert-butyl 3-ethyl 4-oxopiperidine-1,3-dicarboxylate N-Boc-4-Oxo-3-piperidinecarboxylic acid ethyl ester 1-(1,1-Dimethylethyl) 3-ethyl 4-oxo-1,3-piperidinedicarboxylate O1-tert-butyl O3-ethyl 4-oxopiperidine-1,3-dicarboxylate 98977-34-5 77-34-5 C13H21NO5 pharmacetical API intermediates