Cas no 2026-27-9 (1,1'-Biphenyl,3,3',4,4'-tetramethoxy-)
1,1'-Biphenyl,3,3',4,4'-tetramethoxy- Chemical and Physical Properties
Names and Identifiers
-
- 1,1'-Biphenyl,3,3',4,4'-tetramethoxy-
- 3,3',4,4'-TETRAMETHOXY-1,1'-BIPHENYL
- 4-(3,4-dimethoxyphenyl)-1,2-dimethoxybenzene
- 3,3',4,4'-tetramethoxybiphenyl
- 3,3',4,4'-tetramethoxylbiphenyl
- 3,4,3',4'-Tetramethoxy-biphenyl
- 3.4.3'.4'-Tetramethoxy-diphenyl
- AC1L6GXX
- CTK4E3691
- NCIOpen2_007274
- NSC105649
- SureCN8840880
- ZADYUYOJVLZYAQ-UHFFFAOYSA-N
- 3,3',4,4'-Tetramethoxydiphenyl
- 4-(3, 4-dimethoxyphenyl)-1, 2-dimethoxybenzene
- AKOS000277058
- NSC-105649
- SCHEMBL8840880
- 4-(3,4-dimethoxyphenyl)-1,2-dimethoxy-benzene
- 2026-27-9
- DTXSID30295826
- 1,1'-biphenyl, 3,3',4,4'-tetramethoxy-
- 3,4,3',4'-Tetramethoxy diphenyl
-
- Inchi: 1S/C16H18O4/c1-17-13-7-5-11(9-15(13)19-3)12-6-8-14(18-2)16(10-12)20-4/h5-10H,1-4H3
- InChI Key: ZADYUYOJVLZYAQ-UHFFFAOYSA-N
- SMILES: O(C)C1=C(C=CC(=C1)C1C=CC(=C(C=1)OC)OC)OC
Computed Properties
- Exact Mass: 274.12054
- Monoisotopic Mass: 274.120509
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 20
- Rotatable Bond Count: 5
- Complexity: 256
- 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
- Topological Polar Surface Area: 36.9
- XLogP3: 3.4
Experimental Properties
- Density: 1.094
- Boiling Point: 372.9°Cat760mmHg
- Flash Point: 123°C
- Refractive Index: 1.53
- PSA: 36.92
- LogP: 3.38800
1,1'-Biphenyl,3,3',4,4'-tetramethoxy- Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| A2B Chem LLC | AB03904-50mg |
1,1'-Biphenyl, 3,3',4,4'-tetramethoxy- |
2026-27-9 | 95% | 50mg |
$148.00 | 2024-04-20 | |
| A2B Chem LLC | AB03904-100mg |
1,1'-Biphenyl, 3,3',4,4'-tetramethoxy- |
2026-27-9 | 95% | 100mg |
$250.00 | 2024-04-20 | |
| A2B Chem LLC | AB03904-250mg |
1,1'-Biphenyl, 3,3',4,4'-tetramethoxy- |
2026-27-9 | 95% | 250mg |
$424.00 | 2024-04-20 | |
| A2B Chem LLC | AB03904-1g |
1,1'-Biphenyl, 3,3',4,4'-tetramethoxy- |
2026-27-9 | 95% | 1g |
$1144.00 | 2024-04-20 |
1,1'-Biphenyl,3,3',4,4'-tetramethoxy- Related Literature
-
1. Reactions of quinones with aromatic ethers. Part I. Polyalkoxydibenzo[fg,op]naphthacene-1,8-quinones from chloranil and 3,3′,4,4′-tetra-alkoxybiphenylsO. C. Musgrave,C. J. Webster J. Chem. Soc. C 1971 1393
-
O. C. Musgrave,C. J. Webster J. Chem. Soc. D 1969 712
-
3. On the optical activity of the 3-aryl-4-hydroxycoumarin isolated from Millettia griffoniana: molecular modelling and total synthesisSébastien Combes,Jean-Pierre Finet,Didier Siri J. Chem. Soc. Perkin Trans. 1 2002 38
-
4. Novel dibenzo[fg,op]naphthacene discotic liquid crystals: a versatile rational synthesisSandeep Kumar,Jaishri J. Naidu,D. S. Shankar Rao J. Mater. Chem. 2002 12 1335
-
5. Electrochemical control of bridging ligand conformation in a binuclear complex—A possible basis for a molecular switchLaurent F. Joulié,Erik Schatz,Michael D. Ward,Frank Weber,Lesley J. Yellowlees J. Chem. Soc. Dalton Trans. 1994 799
Additional information on 1,1'-Biphenyl,3,3',4,4'-tetramethoxy-
1,1'-Biphenyl,3,3',4,4'-tetramethoxy (CAS No. 2026-27-9)
The compound 1,1'-biphenyl,3,3',4,4'-tetramethoxy (CAS No. 2026-27-9) is a highly specialized organic molecule with a unique structure and diverse applications in various scientific and industrial fields. This compound is characterized by its biphenyl core structure with four methoxy groups attached at the 3, 3', 4, and 4' positions of the benzene rings. The presence of these methoxy groups imparts specific electronic and steric properties to the molecule, making it valuable in research and development.
Structure and Properties: The molecular structure of 1,1'-biphenyl,3,3',4,4'-tetramethoxy consists of two benzene rings connected by a single bond (biphenyl system). The methoxy groups (-OCH?) are electron-donating substituents that activate the aromatic rings toward electrophilic substitution reactions. This electronic activation makes the compound useful in various synthetic pathways where controlled reactivity is desired.
Synthesis and Applications: The synthesis of 1,1'-biphenyl derivatives has been extensively studied due to their potential in materials science and pharmaceuticals. Recent research has focused on using this compound as a precursor for synthesizing advanced materials such as organic semiconductors and optoelectronic devices. For instance, studies have shown that derivatives of 1,1'-biphenyl systems can be used to create efficient OLEDs (Organic Light Emitting Diodes) with improved luminous efficiency and stability.
Pharmacological Applications: In the field of pharmacology, 1,1'-biphenyl derivatives have been explored for their potential as drug candidates. Recent findings indicate that certain analogs of this compound exhibit anti-tumor activity by targeting specific signaling pathways in cancer cells. These studies highlight the importance of understanding the structure-activity relationships in biphenyl-based compounds for drug discovery.
Environmental Considerations: While 1,1'-biphenyl compounds are valuable in various applications, their environmental impact remains a critical area of study. Research into the biodegradation and toxicity profiles of these compounds is ongoing to ensure their safe use in industrial processes.
In conclusion, 1,1'-biphenyl derivatives, particularly those with multiple methoxy substituents like 1,1'-biphenyl-3-carboxylic acid, continue to be a focal point in scientific research due to their versatile properties and wide-ranging applications.
2026-27-9 (1,1'-Biphenyl,3,3',4,4'-tetramethoxy-) Related Products
- 17423-55-1(3,4-dimethoxy-1,1'-Biphenyl)
- 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
- 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
- 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
- 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)
- 1270529-38-8(1,2,3,4,5,6-Hexahydro-[2,3]bipyridinyl-6-ol)
- 941977-17-9(N'-(3-chloro-2-methylphenyl)-N-2-(dimethylamino)-2-(naphthalen-1-yl)ethylethanediamide)
- 2138166-62-6(2,2-Difluoro-3-[methyl(2-methylbutyl)amino]propanoic acid)
- 89640-58-4(2-Iodo-4-nitrophenylhydrazine)
- 1449132-38-0(3-Fluoro-5-(2-fluoro-5-methylbenzylcarbamoyl)benzeneboronic acid)