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Thermo Scientific Chemicals
1-Pyrrolidinecarbonyl chloride, 97%
CAS: 1192-63-8 | C5H8ClNO | 133.575 g/mol
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Catalog number L13396.06
also known as L13396-06
Price (EUR)
111,00
Each
Quantity:
5 g
Price (EUR)
111,00
Each
Chemical Identifiers
CAS1192-63-8
IUPAC Namepyrrolidine-1-carbonyl chloride
Molecular FormulaC5H8ClNO
InChI KeyXACWJIQLDLUFSR-UHFFFAOYSA-N
SMILESClC(=O)N1CCCC1
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Specifications
Specification Sheet
Specification SheetIdentification (FTIR)Conforms
FormLiquid
Assay (GC)≥96.0%
Appearance (Color)Clear colorless to yellow
Refractive Index1.4905-1.4955 @ 20?C
1-Pyrrolidinecarbonyl chloride, is used in the synthesis of (S)-4-(2-(((benzyloxy)carbonyl)amino)-3-methoxy-3-oxopropyl)phenyl pyrrolidine-1-carboxylate
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
1-Pyrrolidinecarbonyl chloride, is used in the synthesis of (S)-4-(2-(((benzyloxy)carbonyl)amino)-3-methoxy-3-oxopropyl)phenyl pyrrolidine-1-carboxylate
Solubility
It reacts with water.
Notes
Moisture Sensitive. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Keep away from oxidizing agents, bases. Stable under recommended storage conditions.
1-Pyrrolidinecarbonyl chloride, is used in the synthesis of (S)-4-(2-(((benzyloxy)carbonyl)amino)-3-methoxy-3-oxopropyl)phenyl pyrrolidine-1-carboxylate
Solubility
It reacts with water.
Notes
Moisture Sensitive. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Keep away from oxidizing agents, bases. Stable under recommended storage conditions.
RUO – Research Use Only
General References:
- Benjamin Cao et. al. Design, synthesis and binding properties of a fluorescent α9β1/α4β1 integrin antagonist and its application as an in vivo probe for bone marrow haemopoietic stem cells. Organic & Biomolecular Chemistry. 2014, 12,(6), 965-978.
- JR Harrison.; P O'Brien. Asymmetric synthesis of N-substituted (R)-2-[(pyrrolidin-1-yl) methyl] pyrrolidines. Synthetic Communications. 2001, 31,(8), 1155-1160.