Cas no 33295-53-3 (7-Bromo-1-methoxynaphthalene)
7-Bromo-1-methoxynaphthalene Chemical and Physical Properties
Names and Identifiers
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- Naphthalene, 7-bromo-1-methoxy-
- 7-bromo-1-methoxynaphthalene
- BTPIORDWKIZDNM-UHFFFAOYSA-N
- FT-0751482
- AKOS022529180
- MFCD17012269
- AS-32944
- 33295-53-3
- SCHEMBL4310484
- 2-Bromo-8-methoxynaphthalene
- DTXSID40619074
- 7-Bromo-1-methoxynaphthalene
-
- MDL: MFCD17012269
- Inchi: 1S/C11H9BrO/c1-13-11-4-2-3-8-5-6-9(12)7-10(8)11/h2-7H,1H3
- InChI Key: BTPIORDWKIZDNM-UHFFFAOYSA-N
- SMILES: BrC1C=CC2=CC=CC(=C2C=1)OC
Computed Properties
- Exact Mass: 235.98367
- Monoisotopic Mass: 235.98368g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 13
- Rotatable Bond Count: 1
- Complexity: 172
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 4.3
- Topological Polar Surface Area: 9.2?2
Experimental Properties
- PSA: 9.23
7-Bromo-1-methoxynaphthalene Security Information
- Signal Word:warning
- Hazard Statement: H303May be harmful if swallowed+H313Skin contact may be harmful+H333Inhalation may be harmful to the body
- Warning Statement: P264+P280+P305+P351+P338+P337+P313
- Safety Instruction: H303+H313+H333
- Storage Condition:storage at -4℃ (1-2weeks), longer storage period at -20℃ (1-2years)
7-Bromo-1-methoxynaphthalene Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| CHENG DOU FEI BO YI YAO Technology Co., Ltd. | ARK-1216-10g |
7-Bromo-1-methoxynaphthalene |
33295-53-3 | 95 | 10g |
$2000 | 2021-05-11 | |
| TRC | B800280-10mg |
7-Bromo-1-methoxynaphthalene |
33295-53-3 | 10mg |
$ 50.00 | 2022-06-06 | ||
| TRC | B800280-50mg |
7-Bromo-1-methoxynaphthalene |
33295-53-3 | 50mg |
$ 160.00 | 2022-06-06 | ||
| TRC | B800280-100mg |
7-Bromo-1-methoxynaphthalene |
33295-53-3 | 100mg |
$ 250.00 | 2022-06-06 | ||
| Chemenu | CM140180-1g |
7-bromo-1-methoxynaphthalene |
33295-53-3 | 95% | 1g |
$561 | 2021-08-05 | |
| abcr | AB447082-250 mg |
7-Bromo-1-methoxynaphthalene |
33295-53-3 | 250mg |
€365.70 | 2023-04-22 | ||
| abcr | AB447082-1 g |
7-Bromo-1-methoxynaphthalene |
33295-53-3 | 1g |
€833.10 | 2023-04-22 | ||
| Chemenu | CM140180-1g |
7-bromo-1-methoxynaphthalene |
33295-53-3 | 95% | 1g |
$*** | 2023-05-30 | |
| eNovation Chemicals LLC | D584626-2g |
7-Bromo-1-methoxynaphthalene |
33295-53-3 | 95% | 2g |
$850 | 2025-08-06 | |
| Alichem | A219000372-500mg |
2-Bromo-8-methoxynaphthalene |
33295-53-3 | 98% | 500mg |
$999.60 | 2023-09-02 |
7-Bromo-1-methoxynaphthalene Suppliers
7-Bromo-1-methoxynaphthalene Related Literature
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J. Xu,T. J. Carrocci,A. A. Hoskins Chem. Commun., 2016,52, 549-552
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Gloria Belén Ramírez-Rodríguez,José Manuel Delgado-López,Jaime Gómez-Morales CrystEngComm, 2013,15, 2206-2212
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Abdelaziz Houmam,Emad M. Hamed Chem. Commun., 2012,48, 11328-11330
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Gaurav J. Shah,Eric P.-Y. Chiou,Ming C. Wu,Chang-Jin “CJ” Kim Lab Chip, 2009,9, 1732-1739
Additional information on 7-Bromo-1-methoxynaphthalene
Introduction to Naphthalene, 7-bromo-1-methoxy- (CAS No. 33295-53-3)
Naphthalene, 7-bromo-1-methoxy-, with the chemical formula C10H7BrO, is a brominated and methoxylated derivative of naphthalene. This compound has garnered significant attention in the field of organic synthesis and pharmaceutical research due to its versatile structural framework and potential applications in medicinal chemistry. As a heterocyclic aromatic compound, it serves as a valuable intermediate in the synthesis of various bioactive molecules, including pharmaceuticals and agrochemicals.
The CAS number 33295-53-3 uniquely identifies this compound in scientific literature and industrial applications. Its molecular structure consists of a naphthalene core substituted with a bromine atom at the 7-position and a methoxy group at the 1-position. This specific substitution pattern imparts unique electronic and steric properties, making it a compelling candidate for further functionalization and derivatization.
In recent years, the interest in Naphthalene, 7-bromo-1-methoxy- has surged due to its role as a key precursor in the development of novel therapeutic agents. Researchers have explored its utility in constructing complex scaffolds that mimic natural products and exhibit promising biological activities. For instance, derivatives of this compound have been investigated for their potential antimicrobial, anti-inflammatory, and anticancer properties.
The synthesis of Naphthalene, 7-bromo-1-methoxy- typically involves bromination and methylation reactions on naphthalene or its derivatives. Advanced synthetic methodologies, such as palladium-catalyzed cross-coupling reactions, have been employed to achieve high regioselectivity and yield. These techniques enhance the efficiency of producing this compound in laboratory-scale settings, facilitating further research and development.
One of the most notable applications of Naphthalene, 7-bromo-1-methoxy- is in the synthesis of kinase inhibitors. Kinases are enzymes involved in numerous cellular processes, and their dysregulation is often associated with diseases such as cancer. By incorporating this compound into drug candidates, researchers aim to develop selective kinase inhibitors that can modulate signaling pathways aberrantly activated in disease states. Preliminary studies have shown that certain derivatives exhibit inhibitory activity against specific kinases, highlighting their therapeutic potential.
The pharmaceutical industry has also explored Naphthalene, 7-bromo-1-methoxy- as a building block for antiviral drugs. The structural features of this compound allow for the design of molecules that can interact with viral enzymes or receptors, thereby inhibiting viral replication. Recent advancements in medicinal chemistry have led to the discovery of novel antiviral agents derived from brominated naphthalenes, demonstrating the importance of this scaffold in drug discovery.
Moreover, agrochemical researchers have utilized Naphthalene, 7-bromo-1-methoxy- to develop new pesticides and herbicides. The compound’s ability to undergo further functionalization enables the creation of molecules with enhanced efficacy against pests while maintaining environmental safety. Such developments are crucial for addressing the growing challenges in global food security and sustainable agriculture.
The chemical properties of Naphthalene, 7-bromo-1-methoxy- make it an attractive candidate for material science applications as well. Its aromatic structure and substituents contribute to its solubility and reactivity, making it suitable for use in organic electronics and polymer chemistry. Researchers are investigating its potential use in developing conductive polymers and organic semiconductors, which could revolutionize technologies such as flexible electronics and solar cells.
In conclusion, Naphthalene, 7-bromo-1-methoxy- (CAS No. 33295-53-3) is a multifaceted compound with significant implications across various scientific disciplines. Its role as an intermediate in pharmaceutical synthesis underscores its importance in drug development efforts aimed at treating diverse diseases. As research continues to uncover new applications for this molecule, Naphthalene, 7-bromo-1-methoxy- is poised to remain a cornerstone of innovation in organic chemistry and related fields.
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