55379-71-0

Basic information

• Product Name: PYRROLIDINE-1-CARBOXYLIC ACID PHENYL ESTER
• Synonyms: PYRROLIDINE-1-CARBOXYLIC ACID PHENYL ESTER
• CAS NO: 55379-71-0
• Molecular Formula: C₁₁H₁₃NO₂
• Molecular Weight: 191.23
• Mol File: 55379-71-0.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 293.4°Cat760mmHg
• Flash Point: 131.2°C
• Appearance: /
• Density: 1.173g/cm³
• Vapor Pressure: 0.00173mmHg at 25°C
• Refractive Index: 1.562
• CAS DataBase Reference: PYRROLIDINE-1-CARBOXYLIC ACID PHENYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: PYRROLIDINE-1-CARBOXYLIC ACID PHENYL ESTER(55379-71-0)
• EPA Substance Registry System: PYRROLIDINE-1-CARBOXYLIC ACID PHENYL ESTER(55379-71-0)

Safety Data

• Hazardous Substances Data: 55379-71-0(Hazardous Substances Data)

Usage

Description

PYRROLIDINE-1-CARBOXYLIC ACID PHENYL ESTER is a versatile chemical compound derived from pyrrolidine and phenyl ester. It is characterized by its high chemical stability and low toxicity, making it a valuable component in various industries.

Uses

Used in Pharmaceutical Industry:
PYRROLIDINE-1-CARBOXYLIC ACID PHENYL ESTER is used as a building block for the synthesis of various pharmaceuticals. Its unique structure allows it to be incorporated into the development of new drugs, contributing to the advancement of medicine.
Used in Organic Synthesis:
In the field of organic synthesis, PYRROLIDINE-1-CARBOXYLIC ACID PHENYL ESTER serves as a reagent, facilitating the creation of a wide range of organic compounds. Its versatility in reactions makes it an essential component in the synthesis process.
Used as a Precursor for Agrochemicals:
PYRROLIDINE-1-CARBOXYLIC ACID PHENYL ESTER is utilized as a precursor in the synthesis of agrochemicals, playing a crucial role in the development of pesticides and other agricultural products that contribute to increased crop yields and protection against pests.
Used in Flavor and Fragrance Industry:
This chemical compound is also employed in the production of flavors and fragrances, adding to the diverse applications of PYRROLIDINE-1-CARBOXYLIC ACID PHENYL ESTER. Its ability to contribute to the creation of various scents and tastes makes it a valuable asset in this industry.

InChI:InChI=1/C11H13NO2/c13-11(12-8-4-5-9-12)14-10-6-2-1-3-7-10/h1-3,6-7H,4-5,8-9H2

Upstream product

• 34085-53-5 phenyl bis(2-hydroxyethyl)carbamate 
• 1192-63-8 1-pyrrolidinecarbonyl chloride 
• 108-95-2 phenol 
• 100-66-3 methoxybenzene 
• 10130-87-7 o-Methoxybenzenesulfonyl chloride 
• 123-75-1 pyrrolidine 
• 1885-14-9 phenyl chloroformate 
• 681439-88-3 1-(2-methoxy-benzenesulfonyl)-pyrrolidine 

Downstream Products

• 1092074-43-5 3-(N-(phenoxycarbonyl)formamido)propanoic acid 
• 121751-70-0 1-phenoxycarbonyl-2-oxopyrrolidine 
• 98841-68-0 (2-hydroxy-phenyl)(pyrrolidin-1-yl)methanone 
• 69001-14-5 2-methoxy-pyrrolidine-1-carboxylic acid phenyl ester 
• 1414838-08-6 (E)-2-(3-ethoxy-3-oxoprop-1-en-1-yl)phenyl pyrrolidine-1-carboxylate 

Relevant articles and documents

Nickel-catalyzed reductive cyclization of alkyl dihalides

The reductive coupling protocol to intramolecular cyclization of dihaloalkanes is presented. It leads to five- and six-membered rings, with the former being more efficient. The incorporation of secondary alkyl halides generally promotes coupling efficiency. To the best of our knowledge, this is the first catalytic ring-closure reaction arising from dihaloalkanes under chemical reductive conditions.

Achieving functional group diversity in parallel synthesis: solution-phase synthesis of a library of ureas, carbamates, thiocarbamates, and amides using carbamoylimidazolium salts

A convenient protocol for the parallel solution-phase synthesis of a library of thiocarbamates, ureas, carbamates, and amides from carbamoylimidazolium salts has been developed. The crystalline carbamoylimidazolium salts are readily synthesized from secon

AZAARENE DERIVATIVES

A compound represented by the general formula: wherein X1 represents a nitrogen atom or a group represented by the formula -CR10=; X2 represents a nitrogen atom or a group represented by the formula -CR11=; Y represents an oxygen atom or the like; R1 represents a C1-6 alkoxy group, an optionally substituted C6-10 aryloxy group, a group represented by the formula -NR12aR12b or the like; R2 represents a hydrogen atom, an optionally substituted C1-6 alkyl group, or the like; R3, R4, R5, R6, R7, R8, R10 and R11 each independently represent a hydrogen atom, a halogen atom, an optionally substituted C1-6 alkyl group, or the like; R9 represents a group represented by the formula -NR16aR16b or the like; and R12a, R12b, R16a and R16b each independently represent a hydrogen atom, an optionally substituted C1-6 alkyl group, or the like, a salt thereof, or a hydrate of the foregoing.