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

General Description

PYRROLIDINE-1-CARBOXYLIC ACID PHENYL ESTER is a chemical compound that is derived from pyrrolidine and phenyl ester. It is commonly used in the production of pharmaceuticals and in organic synthesis as a reagent. The compound has a wide range of applications, including as a building block for various organic compounds, and as a precursor for the synthesis of drugs and agrochemicals. It is also used in the production of flavors and fragrances. PYRROLIDINE-1-CARBOXYLIC ACID PHENYL ESTER is known for its high chemical stability and low toxicity, making it a versatile and valuable chemical compound in various industries.

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

• 123-75-1 pyrrolidine 
• 1885-14-9 phenyl chloroformate 
• 100-66-3 methoxybenzene 
• 108-95-2 phenol 
• 34085-53-5 phenyl bis(2-hydroxyethyl)carbamate 
• 1192-63-8 1-pyrrolidinecarbonyl chloride 
• 10130-87-7 o-Methoxybenzenesulfonyl chloride 
• 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 
• 1414838-08-6 (E)-2-(3-ethoxy-3-oxoprop-1-en-1-yl)phenyl pyrrolidine-1-carboxylate 
• 69001-14-5 2-methoxy-pyrrolidine-1-carboxylic acid phenyl ester 

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.