≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Application
6-Bromopurine is a brominated derivative of purine used in various organic syntheses. Used in the synthesis of several benzo-fused scaffolds with purine or pyrimidine moietes which display antitumor and anticancer properties.
| Pubchem Sid | 504763509 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504763509 |
| Sonrisas canónicas | C1=NC2=C(N1)C(=NC=N2)Br |
| IUPAC Name | 6-bromo-7H-purine |
| InChIKey | CTGFGRDVWBZYNB-UHFFFAOYSA-N |
| INCHI | 1S/C5H3BrN4/c6-4-3-5(9-1-7-3)10-2-8-4/h1-2H,(H,7,8,9,10) |
| Isómeros SMILES | C1=NC2=C(N1)C(=NC=N2)Br |
| WGK Alemania | 3 |
| RTECS | UO7513000 |
| Peso molecular | 199.01 |
| Reaxy-Rn | 5775 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=5775&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Clase | Imidazopyrimidines |
| Subclass | Purines and purine derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Purines and purine derivatives |
| Alternative Parents | Halopyrimidines Aryl bromides Imidazoles Heteroaromatic compounds Azacyclic compounds Organonitrogen compounds Organobromides Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Purine - Halopyrimidine - Pyrimidine - Aryl halide - Aryl bromide - Heteroaromatic compound - Imidazole - Azole - Azacycle - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Organobromide - Organohalogen compound - Aromatic heteropolycyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as purines and purine derivatives. These are aromatic heterocyclic compounds containing a purine moiety, which is formed a pyrimidine-ring ring fused to an imidazole ring. |
| External Descriptors | Not available |
| Solubilidad | DMSO (Slightly), Methanol (Slightly) |
|---|---|
| Punto de fusión (°C) | >300°C |
| Peso molecular | 199.010 g/mol |
| XLogP3 | 1.300 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 0 |
| Exact Mass | 197.954 Da |
| Monoisotopic Mass | 197.954 Da |
| Topological Polar Surface Area | 54.500 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 131.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Yu Sun, Guanghua Lu, Peng Zhang, Ying Wang, Xin Ling, Qi Xue, Zhenhua Yan, Jianchao Liu. (2022) Natural colloids at environmentally relevant concentrations affect the absorption and removal of benzophenone-3 in zebrafish. ENVIRONMENTAL POLLUTION, [PMID:35948112] [10.1016/j.envpol.2022.119860] |
| 2. Ping He, Qian Zheng, Matin Naghizadeh, Guiqi Huang, Sheying Dong. (2024) Efficient and recycled magnetic self-stirring hollow fiber-solid/liquid phase system: An extraction and removal technique for personal care pollutants. JOURNAL OF MOLECULAR LIQUIDS, [PMID:] [10.1016/j.molliq.2024.124002] |
| 3. Yu-Jia Lin, Hong-Mei Li, Yan-Rong Gao, Ping-Fan Wu, Bin Cheng, Chen-Long Yu, Yu-Xin Sheng, Hai-Ming Xu. (2024) Environmentally relevant concentrations of benzophenones exposure disrupt intestinal homeostasis, impair the intestinal barrier, and induce inflammation in mice. ENVIRONMENTAL POLLUTION, [PMID:38614423] [10.1016/j.envpol.2024.123948] |
K2204003