39959-59-6
39959-59-6
Chemical Structure
4-Iodobenzylamine
Synonym(s): (4-Iodophenyl)methanamine
- CAS No.: 39959-59-6
- Formula:C7H8IN
- Molecular Weight:233.05
IUPAC Name: (4-Iodophenyl)methanamine
InChIKey: KCGZGJOBKAXVSU-UHFFFAOYSA-N
SMILES: IC1=CC=C(CN)C=C1
Biological Activity: 4-Iodobenzylamine ((4-Iodophenyl)methanamine) is a probe that can detect the binding patterns of serine proteases that are like trypsin, as well as urokinase-type plasminogen activator (uPA). 4-Iodobenzylamine is stable in aqueous solution[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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4-Iodobenzylamine | 99.84% | 4-Iodobenzylamine ((4-Iodophenyl)methanamine) is a probe that can detect the binding patterns of serine proteases that are like trypsin, as well as urokinase-type plasminogen activator (uPA). 4-Iodobenzylamine is stable in aqueous solution. | ||||||||||||||||||||
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4-Iodoamphetamine hydrochloride | 4-Iodoamphetamine (p-Iodoamphetamine) hydrochloride is a halogenated amphetamine featuring an iodine atom at the para position of the phenyl group. 4-Iodoamphetamine hydrochloride selectively induces serotonin release and inhibits reuptake by rat brain synaptosomes. | |||||||||||||||||||||
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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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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-Iodobenzaldehyde | 99.93% | 4-Iodobenzaldehyde is an aromatic halobenzaldehyde derivative and synthetic intermediate. 4-Iodobenzaldehyde is used for the synthesis of various bioactive molecules such as chalcones, heterocycles, receptor antagonists and channel blockers. | ||||||||||||||||||||
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4-Hydroxybenzylamine (Standard) | ≥98% | 4-Hydroxybenzylamine (Standard) is the analytical standard of 4-Hydroxybenzylamine (HY-W004078). This product is intended for research and analytical applications. 4-Hydroxybenzylamine is a dimerizer and precursor. 4-Hydroxybenzylamine forms cyclic dimers stabilized by O-H/N hydrogen bonds and π-stacking interactions in solution. 4-Hydroxybenzylamine undergoes condensation with formaldehyde to form a 12-atom azacyclophane, facilitated by pre-organization into cyclic dimeric templates. | ||||||||||||||||||||
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1,4-Diiodobenzene | 99.88% | 1,4-Diiodobenzene is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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4-(Aminomethyl)benzonitrile hydrochloride | 99.90% | 4-(Aminomethyl)benzonitrile hydrochloride is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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1,4-Bis(aminomethyl)benzene | 99.91% | 1,4-Bis(aminomethyl)benzene is a PROTAC linker that can be used in the synthesis of PROTACs. | ||||||||||||||||||||
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4-Iodobenzylamine hydrochloride | 4-Iodobenzylamine hydrochloride ((4-Iodophenyl)methanamine hydrochloride) is a probe that can detect the binding patterns of serine proteases that are like trypsin, as well as urokinase-type plasminogen activator (uPA). | |||||||||||||||||||||
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Bengamin hydrochloride | Bengamin (4-(Aminomethyl)phenol) hydrochloride is a drug intermediate that can be used for the synthesis of benzylguanidine derivatives, and it possesses antibacterial activity. | |||||||||||||||||||||
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References
- [1]. Longguang Jiang, et al. Halogen bonding for the design of inhibitors by targeting the S1 pocket of serine proteases. RSC Advances. 2018, 8, 28189. [Content Brief]
- [2]. Goutam Pramanik, et al. Inverse heavy-atom effect in near infrared photoluminescent gold nanoclusters. Nanoscale. 2021 Jun 17;13(23):10462-10467. [Content Brief]
