538-75-0
538-75-0
Chemical Structure
N,N-Dicyclohexylcarbodiimide(DCC)
- CAS No.: 538-75-0
- Formula:C13H22N2
- Molecular Weight:206.33
IUPAC Name: dicyclohexylmethanediimine
InChIKey: QOSSAOTZNIDXMA-UHFFFAOYSA-N
SMILES: C1(N=C=NC2CCCCC2)CCCCC1
Biological Activity: N,N-Dicyclohexylcarbodiimide(DCC) is a dehydrating and condensing agent. N,N-Dicyclohexylcarbodiimide(DCC) enhances adenylate cyclase activity. N,N-Dicyclohexylcarbodiimide(DCC) inhibits amine accumulation. N,N-Dicyclohexylcarbodiimide(DCC) is used to prepare 3-phenylcoumarin derivatives, sulfated derivatives of purslane polysaccharides[1][2][3][4][5][6].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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N,N-Dicyclohexylcarbodiimide(DCC) | 99.43% | N,N-Dicyclohexylcarbodiimide(DCC) is a dehydrating and condensing agent. N,N-Dicyclohexylcarbodiimide(DCC) enhances adenylate cyclase activity. N,N-Dicyclohexylcarbodiimide(DCC) inhibits amine accumulation. N,N-Dicyclohexylcarbodiimide(DCC) is used to prepare 3-phenylcoumarin derivatives, sulfated derivatives of purslane polysaccharides. | ||||||||||||||||||||
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N,N-Dicyclohexylcarbodiimide(DCC) (Standard) | 99.16% | N,N-Dicyclohexylcarbodiimide(DCC) (Standard) is the analytical standard of N,N-Dicyclohexylcarbodiimide(DCC). This product is intended for research and analytical applications. N,N-Dicyclohexylcarbodiimide(DCC) is a dehydrating and condensing agent. N,N-Dicyclohexylcarbodiimide(DCC) enhances adenylate cyclase activity. N,N-Dicyclohexylcarbodiimide(DCC) inhibits amine accumulation. N,N-Dicyclohexylcarbodiimide(DCC) is used to prepare 3-phenylcoumarin derivatives, sulfated derivatives of purslane polysaccharides. | ||||||||||||||||||||
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References
- [1]. Suchi R, et al. Covalent modification of the amine transporter with N,N'-dicyclohexylcarbodiimide. Biochemistry. 1991 Jul 2;30(26):6490-4. [Content Brief]
- [2]. Azulai R, et al. Uncoupling of gonadotropin-sensitive adenylate cyclase by N,N'-dicyclohexylcarbodiimide. Evidence for modification of two sites. Mol Cell Endocrinol. 1980 Apr;18(1):1-10. [Content Brief]
- [3]. Al-Sheddi ES, et al. Novel all trans-retinoic Acid derivatives: cytotoxicity, inhibition of cell cycle progression and induction of apoptosis in human cancer cell lines. Molecules. 2015 May 7;20(5):8181-97. [Content Brief]
- [4]. Chen T, et al. Sulfated modification and cytotoxicity of Portulaca oleracea L. polysaccharides. Glycoconj J. 2010 Aug;27(6):635-42. [Content Brief]
- [5]. Sashidhara KV, et al. Discovery and synthesis of novel 3-phenylcoumarin derivatives as antidepressant agents. Bioorg Med Chem Lett. 2011 Apr 1;21(7):1937-41. [Content Brief]
- [6]. Kim KS, et al. Oral Nanoparticles Exhibit Specific High-Efficiency Intestinal Uptake and Lymphatic Transport. ACS Nano. 2018 Sep 25;12(9):8893-8900. [Content Brief]
