122775-20-6
122775-20-6
Chemical Structure
2-Chloroacetamide-d4
- CAS No.: 122775-20-6
- Formula:C2D4ClNO
- Molecular Weight:97.54
IUPAC Name: 2-chloroacetamide-N,N,2,2-d4
InChIKey: VXIVSQZSERGHQP-BGOGGDMHSA-N
SMILES: ClC([2H])([2H])C(N([2H])[2H])=O
Biological Activity: 2-Chloroacetamide-d4 is the deuterium labeled 2-Chloroacetamide[1]. 2-Chloroacetamide is a preservative and is a herbicide for both uplands and paddy fields. 2-Chloroacetamide is a biocide in agriculture, glues, paints and coatings. 2-Chloroacetamide inhibits very-long-chain fatty acid elongase[2][3][4].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
2-Chloroacetamide-d4 | 2-Chloroacetamide-d4 is the deuterium labeled 2-Chloroacetamide. 2-Chloroacetamide is a preservative and is a herbicide for both uplands and paddy fields. 2-Chloroacetamide is a biocide in agriculture, glues, paints and coatings. 2-Chloroacetamide inhibits very-long-chain fatty acid elongase. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
2-Chloroacetamide (Standard) | 99.80% | 2-Chloroacetamide (Standard) is the analytical standard of 2-Chloroacetamide. This product is intended for research and analytical applications. 2-Chloroacetamide is a preservative and is a herbicide for both uplands and paddy fields. 2-Chloroacetamide is a biocide in agriculture, glues, paints and coatings. 2-Chloroacetamide inhibits very-long-chain fatty acid elongase. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
2-Chloroacetamide | 99.89% | 2-Chloroacetamide is a preservative and is a herbicide for both uplands and paddy fields. 2-Chloroacetamide is a biocide in agriculture, glues, paints and coatings. 2-Chloroacetamide inhibits very-long-chain fatty acid elongase. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
References
- [1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216. [Content Brief]
- [2]. Hidenori Okamoto, et al. Synthesis and Herbicidal Activity of N(1-Arylethenyl)-2-chloroacetamides. Agricultural and Biological Chemistry, Volume 55, 1991-Issue 11.
- [3]. A Fonia, et al. Active Sensitization to Chloracetamide. Contact Dermatitis. 2009 Jan60(1):58-9. [Content Brief]
- [4]. Christian Eckermann, et al. Covalent Binding of Chloroacetamide Herbicides to the Active Site Cysteine of Plant Type III Polyketide Synthases. Phytochemistry. 2003 Nov64(6):1045-54. [Content Brief]
