Chloromethyl pivalate - ≥99% , CAS No.18997-19-8

CAS: 18997-19-8 Cat. No.: C121587 Molecular Weight: 150.6 Beilstein Registry Number: 1560838 EC Number: 242-735-1

GRADE & PURITY ≥99%

Synonyms

AC-ASP-GLU-VAL-ASP-H | AS-19276 | SR-01000944704-1 | SMR000009000 | ZQU16YZ6MF | ((TERT-BUTYLCARBONYL)OXY)METHYL CHLORIDE | pivaloxymethyl chloride | InChI=1/C6H11ClO2/c1-6(2,3)5(8)9-4-7/h4H2,1-3H3 | Pivalic acid chloromethyl ester | Pivaloyloxymethyl chl

Storage

Room temperature,Argon charged

Shipped In

Normal

Overview

Chloromethyl pivalate reacts with sodium salt of sulbactam to yield sulbactam pivoxil. It undergoes acylation reaction with 9-(2-phosphonylmethoxyethyl)adenine (PMEA) to yield bis(pivaloyloxymethyl) PMEA.

Specifications

Synonyms

AC-ASP-GLU-VAL-ASP-H | AS-19276 | SR-01000944704-1 | SMR000009000 | ZQU16YZ6MF | ((TERT-BUTYLCARBONYL)OXY)METHYL CHLORIDE | pivaloxymethyl chloride | InChI=1/C6H11ClO2/c1-6(2, 3)5(8)9-4-7/h4H2, 1-3H3 | Pivalic acid chloromethyl ester | Pivaloyloxymethyl chl

Specifications & Purity

≥99%

Storage

Room temperature, Argon charged

Shipped In

Normal

Purity

≥99%

Names and Identifiers

• Pubchem Sid: 488186453
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488186453
• Canonical Smiles: CC(C)(C)C(=O)OCCl
• IUPAC Name: chloromethyl 2,2-dimethylpropanoate
• InChIKey: GGRHYQCXXYLUTL-UHFFFAOYSA-N
• INCHI: 1S/C6H11ClO2/c1-6(2,3)5(8)9-4-7/h4H2,1-3H3
• Isomeric SMILES: CC(C)(C)C(=O)OCCl
• WGK Germany: 3
• Molecular Weight: 150.6
• Beilstein: 1560838
• Reaxy-Rn: 1560838
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1560838&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Class Carboxylic acids and derivatives
      • Subclass Carboxylic acid derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: Carboxylic acids and derivatives
• Subclass: Carboxylic acid derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Carboxylic acid esters
• Alternative Parents: Monocarboxylic acids and derivatives Organochlorides Organic oxides Hydrocarbon derivatives Carbonyl compounds Alkyl chlorides
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Carboxylic acid ester - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organochloride - Organohalogen compound - Carbonyl group - Alkyl halide - Alkyl chloride - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as carboxylic acid esters. These are carboxylic acid derivatives in which the carbon atom from the carbonyl group is attached to an alkyl or an aryl moiety through an oxygen atom (forming an ester group).
• 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: Miscible with most organic solvents. Immiscible with water.
• Sensitivity: Moisture sensitive
• Refractive Index: 1.417
• Flash Point(°F): 104 °F
• Flash Point(°C): 40°C
• Boil Point(°C): 147°C
• Molecular Weight: 150.600 g/mol
• XLogP3: 2.200
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 150.045 Da
• Monoisotopic Mass: 150.045 Da
• Topological Polar Surface Area: 26.300 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 104.000
• 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