233600-80-1
233600-80-1
Chemical Structure
4-Iodoaniline-13C6
- CAS No.: 233600-80-1
- Formula:13C6H6IN
- Molecular Weight:224.98
IUPAC Name: 4-iodoaniline-13C6
InChIKey: VLVCDUSVTXIWGW-IDEBNGHGSA-N
SMILES: I[13C]1=[13CH][13CH]=[13C]([13CH]=[13CH]1)N
Biological Activity: 4-Iodoaniline-13C6 is the 13C labeled 4-Iodoaniline (HY-I0210). 4-Iodoaniline is a potent methemoglobin former. 4-Iodoaniline is also an intermediate. 4-Iodoaniline can be used to synthesize glycogen phosphorylase inhibitors. 4-Iodoaniline is used in the research of liver cancer and blood diseases[1][2].
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4-Iodoaniline-13C6 | 99.17% | 4-Iodoaniline-13C6 is the 13C labeled 4-Iodoaniline (HY-I0210). 4-Iodoaniline is a potent methemoglobin former. 4-Iodoaniline is also an intermediate. 4-Iodoaniline can be used to synthesize glycogen phosphorylase inhibitors. 4-Iodoaniline is used in the research of liver cancer and blood diseases. | ||||||||||||||||||||
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4-Iodoaniline, 98% | 99.97% | 4-Iodoaniline is a potent methemoglobin former. 4-Iodoaniline is also an intermediate. 4-Iodoaniline can be used to synthesize glycogen phosphorylase inhibitors. 4-Iodoaniline is used in the research of liver cancer and blood diseases. | ||||||||||||||||||||
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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]. Mahmud R, et al. Structural basis for the haemotoxicity of dapsone: the importance of the sulphonyl group. Toxicology. 1997 Feb 14;117(1):1-11. [Content Brief]
Keywords
