N-Trimethylsilyl-2-pyrrolidone - ≥95% , CAS No.14468-90-7

CAS: 14468-90-7 Cat. No.: N587264 Molecular Weight: 157.29 EC Number: 238-461-7

GRADE & PURITY ≥95%

Synonyms

1-(Trimethylsilyl)-2-pyrrolidinone # | 1-trimethylsilylpyrrolidone | AKOS015898257 | N-trimethylsilyl-2-pyrrolidone | N-trimethylsilylpyrrolid-2-one | 1-trimethylsilylpyrrolidin-2-one | DTXSID50162783 | FT-0605886 | s20275 | E83844 | 1-(Trimethylsilyl)-2-

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Overview

Application：

1-Trimethylsilyl-2-pyrrolidinone, is used as a fine chemical intermediate.

Specifications

Synonyms

1-(Trimethylsilyl)-2-pyrrolidinone # | 1-trimethylsilylpyrrolidone | AKOS015898257 | N-trimethylsilyl-2-pyrrolidone | N-trimethylsilylpyrrolid-2-one | 1-trimethylsilylpyrrolidin-2-one | DTXSID50162783 | FT-0605886 | s20275 | E83844 | 1-(Trimethylsilyl)-2-

Specifications & Purity

≥95%

Storage

Store at 2-8°C, Argon charged

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥95%

Names and Identifiers

• Canonical Smiles: C[Si](C)(C)N1CCCC1=O
• IUPAC Name: 1-trimethylsilylpyrrolidin-2-one
• InChIKey: LUBVCBITQHEVCJ-UHFFFAOYSA-N
• INCHI: 1S/C7H15NOSi/c1-10(2,3)8-6-4-5-7(8)9/h4-6H2,1-3H3
• Isomeric SMILES: C[Si](C)(C)N1CCCC1=O
• WGK Germany: 3
• Molecular Weight: 157.29
• Reaxy-Rn: 114950
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=114950&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Class Pyrrolidines
      • Subclass Pyrrolidones

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Class: Pyrrolidines
• Subclass: Pyrrolidones
• Intermediate Tree Nodes: Not available
• Direct Parent: Pyrrolidine-2-ones
• Alternative Parents: Trialkylheterosilanes Lactams Organic metalloid salts N-silyl compounds Carboxylic acids and derivatives Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: 2-pyrrolidone - Trialkylheterosilane - Lactam - Carboxylic acid derivative - N-silyl compound - Organic metalloid salt - Azacycle - Organoheterosilane - Organic nitrogen compound - Organic salt - Organosilicon compound - Carbonyl group - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organic oxygen compound - Organopnictogen compound - Aliphatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as pyrrolidine-2-ones. These are pyrrolidines which bear a C=O group at position 2 of the pyrrolidine ring.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Solubility: It hydrolyzes with water
• Sensitivity: Moisture Sensitive
• Refractive Index: 1.46
• Flash Point(°F): 127.4 °F
• Flash Point(°C): 53 °C
• Boil Point(°C): 90°/20mm
• Molecular Weight: 157.290 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 157.092 Da
• Monoisotopic Mass: 157.092 Da
• Topological Polar Surface Area: 20.300 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 150.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

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