1121-22-8
1121-22-8
Chemical Structure
trans-1,2-Cyclohexanediamine
- CAS No.: 1121-22-8
- Formula:C6H14N2
- Molecular Weight:114.19
IUPAC Name: (1R,2R)-cyclohexane-1,2-diamine
InChIKey: SSJXIUAHEKJCMH-PHDIDXHHSA-N
SMILES: N[C@H]1[C@@H](CCCC1)N
Biological Activity: trans-1,2-Cyclohexanediamine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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trans-1,2-Cyclohexanediamine | 99.24% | trans-1,2-Cyclohexanediamine 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-trans-Hydroxycyclohexylamine | 99.98% | 4-trans-Hydroxycyclohexylamine (trans-4-Aminocyclohexan-1-ol) is an intermediate. 4-trans-Hydroxycyclohexylamine is used in the synthesis of the PGK1 inhibitor Compd 25-4. 4-trans-Hydroxycyclohexylamine is used in research on EGFR-positive esophageal squamous cell carcinoma. | ||||||||||||||||||||
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trans-1,4-Cyclohexanediamine | trans-1,4-Cyclohexanediamine is a PROTAC linker that can be used in the synthesis of PROTACs. | |||||||||||||||||||||
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Cyclohexane-1,4-diamine | Cyclohexane-1,4-diamine (1,4-Diaminocyclohexane) is a PROTAC Linker and can be used for PROTAC synthesis, such as TYD-68 (HY-173357). | |||||||||||||||||||||
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trans-4-Methylcyclohexanamine | 99.97% | trans-4-Methylcyclohexanamine is an organic amine compound that can be used in the development of T. cruzi enzyme inhibitors. | ||||||||||||||||||||
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trans-4-Aminocyclohexanol hydrochloride | trans-4-Aminocyclohexanol hydrochloride is a PROTAC linker that can be used in the synthesis of PROTACs. | |||||||||||||||||||||
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trans-1,2-Dimethylcyclohexane | trans-1,2-Dimethylcyclohexane is a kind of biological materials or organic compounds that are widely used in life science research. | |||||||||||||||||||||
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4-(2-Aminoethyl)cyclohexan-1-amine | 4-(2-Aminoethyl)cyclohexan-1-amine is a PROTAC linker that can be used in the synthesis of PROTACs. | |||||||||||||||||||||
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