Thienopyridines
eMolecules 823-58-5 | 3,6-Dichloropyridazin-4-amine | Combi-Blocks | MFCD01647253 | 163.990 | C4H3Cl2N3 | 98.000 | Nc1cc(Cl)nnc1Cl | 1g | 117541468
3,6-Dichloropyridazin-4-amine | Combi-Blocks | 823-58-5 | MFCD01647253 | 163.990 | C4H3Cl2N3 | 98.000 | Nc1cc(Cl)nnc1Cl | 1g | 117541468
eMolecules 53180-76-0 | 3,5-Dichloropyridazin-4-amine | ChemScene | MFCD01647251 | 163.990 | C4H3Cl2N3 | 97.000 | Nc1c(Cl)cnnc1Cl | 1g | 486161833
3,5-Dichloropyridazin-4-amine | ChemScene | 53180-76-0 | MFCD01647251 | 163.990 | C4H3Cl2N3 | 97.000 | Nc1c(Cl)cnnc1Cl | 1g | 486161833
Medchemexpress LLC AMI-1 free acid | 134-47-4 | 99.5% | 504.49 | 25 MG
AMI-1 free acid | 134-47-4 | 99.5% | 504.49 | 25 MG
Cell Signaling Technology SSX1/3 (E9P5M) Rabbit mAb (Amino-terminal Antigen) 20 ul
SSX1/3 (E9P5M) Rabbit mAb (Amino-terminal Antigen) 20 ul
![Medchemexpress LLC Carbamic acid, N-[4-(4-amino-3-iodo-1H-pyrazolo[3,4-d]pyrimidin-1-yl)butyl]-, 1,1-dimethylethyl ester | 1887095-79-5 | 95.03% | 432.27 | 1 G](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000400878-logo.png-250.jpg){kind=logo}
Medchemexpress LLC Carbamic acid, N-[4-(4-amino-3-iodo-1H-pyrazolo[3,4-d]pyrimidin-1-yl)butyl]-, 1,1-dimethylethyl ester | 1887095-79-5 | 95.03% | 432.27 | 1 G
tert-Butyl (4-(4-amino-3-iodo-1H-pyrazolo[3,4-d]pyrimidin-1-yl)butyl)carbamate is a chemical compound that serves as a valuable drug intermediate for the synthesis of various active compounds. It is strictly for research purposes and not for direct use with patients. The compound is presented in a solid form.
- Drug intermediate for synthesizing active compounds.
- For research use only.
- Available in solid appearance.
Apexbio Technology LLC Thieno-CTP 50ul (100 mM)
Thieno-CTP is a structural analog of cytidine triphosphate (CTP) that incorporates a thiophene-modified nucleobase allowing incorporation into RNA by RNA polymerases during transcription Following enzymatic incorporation into nascent RNA transcripts the introduced thienyl modification acts as a reactive site suitable for subsequent bioorthogonal labeling via selective chemical reactions This chemical feature enables detection visualization and analysis of newly synthesized RNA molecules within biological systems Hence Thieno-CTP is utilized to examine transcriptional dynamics RNA synthetic regulation RNA trafficking and RNA-protein interaction studies supporting research into RNA biology and related areas