<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">125114</id>
  <title nil="true"/>
  <common-name>2-Chlorooxirane</common-name>
  <description>2-Chlorooxirane is an organic compound with the formula C2H3ClO and an average molecular weight of 78.50 g/mol. 2-Chlorooxirane belongs to the epoxides, a class of organoheterocyclic compounds within the organic compounds.

This compound is found in or released from 13 recorded sources across multiple sectors. Within electrical and electronic equipment, it is associated with cell phones, capacitors, wires and cables, batteries, and printed circuit boards, among one other source. It is found in textiles, leather and furnishings, specifically within carpets, rugs, and synthetic textiles. In the food, food processing and cookware sector, it is linked to food packaging. It is also present in healthcare, pharmaceuticals and veterinary products via medical devices. Additionally, it is found in lubricants used in both industrial manufacturing and chemical processing, as well as in the energy, oil and gas sector. One other sector is also recorded as a source. Recorded exposure routes for 2-chlorooxirane include inhalation, oral, and touch.</description>
  <cas>7763-77-1</cas>
  <pubchem-id>24472</pubchem-id>
  <chemical-formula>C2H3ClO</chemical-formula>
  <weight>78.5</weight>
  <appearance nil="true"/>
  <melting-point nil="true"/>
  <boiling-point nil="true"/>
  <density nil="true"/>
  <solubility nil="true"/>
  <specific-gravity nil="true"/>
  <flash-point nil="true"/>
  <vapour-pressure nil="true"/>
  <route-of-exposure nil="true"/>
  <target nil="true"/>
  <mechanism-of-toxicity nil="true"/>
  <metabolism nil="true"/>
  <toxicity nil="true"/>
  <lethaldose nil="true"/>
  <carcinogenicity nil="true"/>
  <use-source nil="true"/>
  <min-risk-level nil="true"/>
  <health-effects nil="true"/>
  <symptoms nil="true"/>
  <treatment nil="true"/>
  <created-at type="dateTime">2026-04-06T09:01:33Z</created-at>
  <updated-at type="dateTime">2026-08-22T09:35:48Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia nil="true"/>
  <uniprot-id nil="true"/>
  <kegg-compound-id nil="true"/>
  <omim-id nil="true"/>
  <chebi-id nil="true"/>
  <biocyc-id nil="true"/>
  <ctd-id nil="true"/>
  <stitch-id nil="true"/>
  <drugbank-id nil="true"/>
  <pdb-id nil="true"/>
  <actor-id nil="true"/>
  <organism nil="true"/>
  <export type="boolean">true</export>
  <metabolizing-proteins nil="true"/>
  <transporting-proteins nil="true"/>
  <moldb-smiles nil="true"/>
  <moldb-formula>C2H3ClO</moldb-formula>
  <moldb-inchi>InChI=1S/C2H3ClO/c3-2-1-4-2/h2H,1H2</moldb-inchi>
  <moldb-inchikey>WBNCHVFLFSFIGK-UHFFFAOYSA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">78.5</moldb-average-mass>
  <moldb-mono-mass type="decimal">77.9872424</moldb-mono-mass>
  <origin nil="true"/>
  <state nil="true"/>
  <logp>0.6</logp>
  <hmdb-id nil="true"/>
  <chembl-id nil="true"/>
  <chemspider-id nil="true"/>
  <structure-image-file-name nil="true"/>
  <structure-image-content-type nil="true"/>
  <structure-image-file-size type="integer" nil="true"/>
  <structure-image-updated-at type="dateTime" nil="true"/>
  <biodb-id nil="true"/>
  <synthesis-reference nil="true"/>
  <structure-image-caption nil="true"/>
  <chemdb-id>CHEM121007</chemdb-id>
  <dsstox-id nil="true"/>
  <toxcast-id nil="true"/>
  <stoff-ident-origin nil="true"/>
  <stoff-ident-id nil="true"/>
  <susdat-id>NS00115916</susdat-id>
  <iupac>2-chlorooxirane</iupac>
  <moldb-polar-surface-area nil="true"/>
  <moldb-refractivity nil="true"/>
  <moldb-polarizability nil="true"/>
  <moldb-rotatable-bond-count nil="true"/>
  <moldb-acceptor-count nil="true"/>
  <moldb-donor-count nil="true"/>
  <moldb-pka-strongest-acidic nil="true"/>
  <moldb-pka-strongest-basic nil="true"/>
  <moldb-physiological-charge nil="true"/>
  <moldb-number-of-rings nil="true"/>
  <moldb-alogps-logp nil="true"/>
  <moldb-alogps-logs nil="true"/>
  <moldb-alogps-solubility nil="true"/>
  <kingdom>Organic compounds</kingdom>
  <superklass>Organoheterocyclic compounds</superklass>
  <klass>Epoxides</klass>
  <subklass nil="true"/>
  <paper-count type="integer">10</paper-count>
  <sync-id>CED0035712</sync-id>
  <structure-inchikey nil="true"/>
  <structure-fingerprint nil="true"/>
  <structure-pattern-fingerprint nil="true"/>
  <structure-pickle nil="true"/>
  <structure-indexed-at nil="true"/>
</compound>
