Date published: 2025-10-14

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2-Chloroacetamide (CAS 79-07-2)

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CAS Number:
79-07-2
Purity:
≥98%
Molecular Weight:
93.51
Molecular Formula:
C2H4ClNO
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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2-Chloroacetamide is widely used in the field of organic chemistry for research focused on the synthesis and modification of organic compounds. It serves as a versatile reagent that is particularly useful for introducing amide functionalities into molecules, which is a key step in the synthesis of various chemical products. Researchers utilize 2-Chloroacetamide to study its reactivity and the conditions under which it can effectively participate in chemical reactions, such as nucleophilic substitution. Furthermore, it is investigated for its role as a chemical intermediate in the production of herbicides, fungicides, and other industrial chemicals.


2-Chloroacetamide (CAS 79-07-2) References

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  2. Conformation and intramolecular hydrogen bonding of 2-chloroacetamide as studied by microwave spectroscopy and quantum chemical calculations.  |  Møllendal, H. and Samdal, S. 2006. J Phys Chem A. 110: 2139-46. PMID: 16466249
  3. The Impact of Commonly Used Alkylating Agents on Artifactual Peptide Modification.  |  Hains, PG. and Robinson, PJ. 2017. J Proteome Res. 16: 3443-3447. PMID: 28799334
  4. N-Containing α-Mangostin Analogs via Smiles Rearrangement as the Promising Cytotoxic, Antitrypanosomal, and SARS-CoV-2 Main Protease Inhibitory Agents.  |  Pyae, NYL., et al. 2023. Molecules. 28: PMID: 36770770
  5. Mesoporous manganese oxide for the degradation of organophosphates pesticides  |  , et al. (2016). Journal of Materials Science. volume 51,: pages 2634–2642.
  6. Synthesis of 2-oxo and 2-thioxo-3(2H)-benzothiazoleethanimic acid anhydride with acetic acid and related products  |   and. September/October 1988. Journal of Heterocyclic Chemistry. Volume25, Issue5: Pages 1503-1509.
  7. Evaluation of alternative reference toxicants for use in the earthworm toxicity test  |   and. July 1995. Environmental Toxicology and Chemistry. Volume14, Issue7: Pages 1189-1194.
  8. An efficient microwave-assisted synthesis of thieno[2,3- b ]quinolines under solvent-free conditions  |  Belalakatte P. Nandeshwarappa, et al. 2005 -. Journal of Sulfur Chemistry. Volume 26, Issue 4-5: Pages 373-379.
  9. Synthesis, Reactions, and Antiviral Activity of 5′-Acetyl-6′-methyl-2′-thioxo-1′,2′-dihydro-3,4′-bipyridine-3′-carbonitrile  |  Fawzy A. Attaby, et al. 2006 -. Phosphorus, Sulfur, and Silicon and the Related Elements. Volume 181, Issue 1: Pages 1-14.
  10. Mesoporous titanium–manganese dioxide for sulphur mustard and soman decontamination  |  V Štengl, J Bludska, F Opluštil, T Němec - Materials Research Bulletin, 2011 - Elsevier. November 2011,. Materials Research Bulletin. Volume 46, Issue 11,: Pages 2050-2056.
  11. Synthesis, characterization and crystal structure of some novel partially hydrogenated isoquinolines and their fused heterocyclic systems  |   and Islam S. Marae, Omaima F. Ibrahim, Shams H. Abdel-Hafez, Shaaban K. Mohamed, Joel T. Mague, Etify A. -G. Bakhite. July 2022. Journal of Heterocyclic Chemistry. Volume59, Issue7: Pages 1230-1240.
  12. Mesoporous manganese oxide for warfare agents degradation  |  V Štengl, D Králová, F Opluštil, T Němec - Microporous and mesoporous …, 2012 - Elsevier. 1 July 2012,. Elsevier Microporous and Mesoporous Materials. Volume 156,: Pages 224-232.
  13. One-pot conversion of phenols to anilines via Smiles rearrangement  |  YS Xie, BVD Vijaykumar, K Jang, HH Shin, H Zuo… - Tetrahedron …, 2013 - Elsevier. 18 September 2013,. Tetrahedron Letters. Volume 54, Issue 38,: Pages 5151-5154.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2-Chloroacetamide, 250 g

sc-237988
250 g
$36.00