Tert-Butyl 3-cyano-4-oxopyrrolidine-1-carboxylate CAS 175463-32-8

We can provide tert-Butyl 3-cyano-4-oxopyrrolidine-1-carboxylate CAS 175463-32-8 with a certificate of analysis (COA), method of analysis (MOA), route of synthesis (ROS), and material safety data sheet (MSDS)

 

Chemical Properties:

Melting point: 160-167°C

Boiling point: 360.7±42.0 °C at 760 mmHg

Density:1.2±0.1 g/cm3

Flash Point:172.0±27.9 °C

 

Synonyms：

N-BOC-3-CYANO-4-PYRROLIDINONE

N-Boc-3-Cyano-4-Pyrrolidinone

1-N-Boc-3-Cyano-Pyrrolidone-4

1-N-BOC-3-CYANO-PYRROLIDONE-4

1-N-BOC-3-CYANO-PYRROLID-4-ONE

1-Boc-3-cyano-4-oxopyrrolidine

1-N-Boc-3-Cyano-Pyrrolid-4-One

1-N-Boc-3-Cyano-Pyrrolidinone-4

1-Boc-3-Cyano-4-Oxo-Pyrrolidine

1-N-BOC-3-CYANO-PYRROLIDINONE-4

4-CYANO-1-N-BOC PYRROLIDIN-3-ONE

4-Cyano-1-N-Boc Pyrrolidin-3-One

1-N-BOC-4-CYANO-PYRROLIDINE-3-ONE

Tert-Butyl 3-Cyano-4-Oxopyrrolidine-1-Carboxylate

Tert-Butyl-3-Cyano-4-Oxopyrrolidine-1-Carboxylate

4-Cyano-1-N-(Tert-Butoxycarbonyl)Pyrrolidin-3-One

TERT-BUTYL-3-CYANO-4-OXOPYRROLIDINE-1-CARBOXYLATE

3-Cyano-4-Oxo-Pyrrolidine-1-Carboxylic Acid Tert-Butyl Ester

3-CYANO-4-OXO-PYRROLIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER

 

tert-Butyl 3-cyano-4-oxopyrrolidine-1-carboxylate CAS 175463-32-8 is an organic compound. It is a white to light yellow solid with a distinctive odor.

tert-Butyl 3-cyano-4-oxopyrrolidine-1-carboxylate CAS 175463-32-8 is a compound with multiple functional groups. It contains a quaternary ammonium carbonyl (Boc) protecting group, a cyano group and a pyrrolidone ring. The quaternary ammonium carbonyl (Boc) is a protecting group that stabilizes the compound and makes it easier to handle and purify. The cyano group is a nitrogen-containing functional group, while the pyrrolidone is a five-membered heterocycle containing a ketone group.

tert-Butyl 3-cyano-4-oxopyrrolidine-1-carboxylate CAS 175463-32-8 is often used as an intermediate in organic synthesis. It can be synthesized by various methods, such as the reaction of pyrrolidone with Boc-Cl. It can be reduced to the corresponding amine or the Boc-protecting group can be removed by acid hydrolysis reactions.

 

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