Cas no 6843-66-9 (Diphenyldimethoxysilane)
Diphenyldimethoxysilane Chemical and Physical Properties
Names and Identifiers
-
- Dimethoxydiphenylsilane
- Diphenyldimethoxysilane
- Decahydroquinoline, Mixture of cis and trans
- Silane,dimethoxydiphenyl- (6CI,7CI,8CI,9CI)
- AY 43-047
- AZ 6183
- D 6010
- KBM 202
- KBM 202LS5300
- KBM202S
- KBM 202SS
- LS 5300
- NSC 93509
- OF 1
- OF 1 (silane)
- TSL 8172
- Z 6074
- Silane, dimethoxydiphenyl-
- dimethoxy(diphenyl)silane
- Benzene, 1,1'-(dimethoxysilylene)bis-
- AHUXYBVKTIBBJW-UHFFFAOYSA-N
- 02QB6788GC
- AK110726
- diphenyldimethoxy silane
- diphenyldimethoxylsilicane
- diphenyl dimethoxy silane
- dimethoxy-di(phenyl)silane
- Diphenyldimethoxysilane, Min
- DSSTox_CID_24717
- NCIOpen2_005829
- AS-15383
- CAS-6843-66-9
- NSC-93509
- EINECS 229-929-1
- CHEMBL3560757
- FT-0604912
- SCHEMBL49008
- Dimethoxydiphenylsilane, >=95.0% (GC)
- 6843-66-9
- D1731
- DTXSID2044717
- NCGC00357261-01
- J-520385
- SY015724
- C14H16O2Si
- S07875
- Q27231538
- AC2243
- InChI=1/C14H16O2Si/c1-15-17(16-2,13-9-5-3-6-10-13)14-11-7-4-8-12-14/h3-12H,1-2H3
- AHUXYBVKTIBBJW-UHFFFAOYSA-
- DPDMS cpd
- Tox21_303725
- EC 229-929-1
- Gp-235 Dimethoxydiphenylsilane
- AMY39306
- NSC93509
- CD6010
- CS-0113381
- 121536-62-7
- dimethoxy-diphenyl-silane
- AKOS008901136
- NS00044447
- DTXCID0024717
- UNII-02QB6788GC
- MFCD00025690
- DIPHENYLDIMETHOXYSILANE, 98%
- DB-029679
-
- MDL: MFCD00025690
- Inchi: 1S/C14H16O2Si/c1-15-17(16-2,13-9-5-3-6-10-13)14-11-7-4-8-12-14/h3-12H,1-2H3
- InChI Key: AHUXYBVKTIBBJW-UHFFFAOYSA-N
- SMILES: [Si](C1C=CC=CC=1)(C1C=CC=CC=1)(OC)OC
- BRN: 2940458
Computed Properties
- Exact Mass: 244.09200
- Monoisotopic Mass: 244.092
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 17
- Rotatable Bond Count: 4
- Complexity: 196
- 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: 18.5
- Surface Charge: 0
- Tautomer Count: nothing
- XLogP3: nothing
Experimental Properties
- Color/Form: Black powder
- Density: 1.08?g/mL?at 20?°C(lit.)
- Melting Point: <0°C
- Boiling Point: 110°C/1mmHg(lit.)
- Flash Point: Fahrenheit: 249.8 ° f < br / > Celsius: 121 ° C < br / >
- Refractive Index: n20/D 1.5450(lit.)
- PSA: 18.46000
- LogP: 1.53580
- Sensitiveness: Moisture Sensitive
Diphenyldimethoxysilane Security Information
-
Symbol:
- Prompt:warning
- Signal Word:Warning
- Hazard Statement: H315
- Warning Statement: P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
- Hazardous Material transportation number:NONH for all modes of transport
- WGK Germany:2
- Hazard Category Code: 38
- Safety Instruction: S28-S37
- FLUKA BRAND F CODES:10-21
- RTECS:VV3643332
-
Hazardous Material Identification:
- TSCA:Yes
- Storage Condition:Inert atmosphere,Room Temperature
- Risk Phrases:R38
- Safety Term:S26;S36
Diphenyldimethoxysilane Customs Data
- HS CODE:2931900090
- Customs Data:
China Customs Code:
2931900090Overview:
2931900090. Other organic-Inorganic compound. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:AB(Customs clearance form for Inbound Goods,Customs clearance form for outbound goods). MFN tariff:6.5%. general tariff:30.0%
Summary:
2931900090. other organo-inorganic compounds. VAT:17.0%. Tax rebate rate:13.0%. Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward). MFN tariff:6.5%. General tariff:30.0%
Diphenyldimethoxysilane Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Chemenu | CM137609-500g |
Dimethoxydiphenylsilane |
6843-66-9 | 95% | 500g |
$102 | 2021-06-17 | |
| BAI LING WEI Technology Co., Ltd. | 105839-50G |
Dimethoxydiphenylsilane, 98% |
6843-66-9 | 98% | 50G |
¥ 194 | 2022-04-26 | |
| BAI LING WEI Technology Co., Ltd. | 105839-250G |
Dimethoxydiphenylsilane, 98% |
6843-66-9 | 98% | 250G |
¥ 436 | 2022-04-26 | |
| TRC | D493598-1mL |
Diphenyldimethoxysilane |
6843-66-9 | 1mL |
$ 50.00 | 2022-06-05 | ||
| TRC | D493598-2mL |
Diphenyldimethoxysilane |
6843-66-9 | 2mL |
$ 65.00 | 2022-06-05 | ||
| TRC | D493598-10mg |
Diphenyldimethoxysilane |
6843-66-9 | 10mg |
$ 80.00 | 2022-06-05 | ||
| Fluorochem | S07875-25g |
Diphenyldimethoxysilane(Dimethoxydiphenylsilane) |
6843-66-9 | 95+% | 25g |
£12.00 | 2022-02-28 | |
| Fluorochem | S07875-100g |
Diphenyldimethoxysilane(Dimethoxydiphenylsilane) |
6843-66-9 | 95+% | 100g |
£19.00 | 2022-02-28 | |
| Fluorochem | S07875-500g |
Diphenyldimethoxysilane(Dimethoxydiphenylsilane) |
6843-66-9 | 95+% | 500g |
£65.00 | 2022-02-28 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | D107998-25ml |
Diphenyldimethoxysilane |
6843-66-9 | 98% | 25ml |
¥29.90 | 2023-09-03 |
Diphenyldimethoxysilane Suppliers
Diphenyldimethoxysilane Related Literature
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Tao Wang,Yangyang Liu,Yue Deng,Hongbo Fu,Jianmin Chen Environ. Sci.: Nano, 2018,5, 1821-1833
-
Yaling Zhang,Chunhui Dai,Shiwei Zhou,Bin Liu Chem. Commun., 2018,54, 10092-10095
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Abdelaziz Houmam,Emad M. Hamed Chem. Commun., 2012,48, 11328-11330
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Eléonore Resongles,Corinne Casiot,Fran?oise Elbaz-Poulichet,Rémi Freydier,Odile Bruneel,Christine Piot,Sophie Delpoux,Aurélie Volant,Angélique Desoeuvre Environ. Sci.: Processes Impacts, 2013,15, 1536-1544
-
Weili Dai,Guangjun Wu,Michael Hunger Chem. Commun., 2015,51, 13779-13782
Additional information on Diphenyldimethoxysilane
Diphenyldimethoxysilane (CAS No. 6843-66-9): Applications and Recent Advances in Chemical Research
Diphenyldimethoxysilane, chemically designated as Diphenyldimethoxysilane (CAS No. 6843-66-9), is a versatile organosilicon compound that has garnered significant attention in the field of chemical research due to its unique structural and functional properties. This compound, characterized by a silane backbone with two methoxy groups and two phenyl substituents, exhibits remarkable reactivity and adaptability, making it a valuable intermediate in synthetic chemistry, material science, and pharmaceutical development.
The molecular structure of Diphenyldimethoxysilane consists of a central silicon atom bonded to two methoxy groups (–OCH?) and two phenyl groups (–C?H?). This arrangement imparts distinct chemical behavior, enabling the compound to participate in various reactions such as hydrolysis, condensation, and cross-coupling processes. The presence of phenyl groups enhances the compound's stability and compatibility with organic systems, while the methoxy groups provide reactive sites for further functionalization.
In recent years, Diphenyldimethoxysilane has been extensively studied for its potential applications in the synthesis of advanced materials. One notable area of research involves its use as a precursor in the preparation of siloxane polymers and coatings. These materials exhibit excellent thermal stability, chemical resistance, and mechanical strength, making them suitable for high-performance applications in industries such as aerospace, automotive, and electronics. The phenyl groups in the molecule contribute to the polymer's hydrophobicity, while the methoxy groups facilitate cross-linking reactions, resulting in robust network structures.
Another emerging application of Diphenyldimethoxysilane is in the field of pharmaceuticals. Researchers have explored its utility as a building block for designing novel drug molecules with enhanced bioavailability and targeted delivery systems. The silane core can be modified to incorporate pharmacophores that interact with biological targets, while the methoxy and phenyl groups provide structural stability and metabolic resistance. Recent studies have demonstrated its role in synthesizing antiviral and anti-inflammatory agents, where the compound's ability to form stable complexes with therapeutic molecules is leveraged.
The compound's reactivity also makes it a valuable tool in organic synthesis. For instance, Diphenyldimethoxysilane can be used to introduce silicon-based functionalities into organic molecules through nucleophilic substitution reactions. This approach has been employed in the synthesis of complex heterocyclic compounds, which are prevalent in many biologically active molecules. The ability to selectively modify specific positions on the organic framework using Diphenyldimethoxysilane offers chemists greater control over molecular architecture, enabling the creation of tailored compounds with desired properties.
In addition to its synthetic applications, Diphenyldimethoxysilane has found utility in catalysis. The compound's silicon-centered structure can act as a ligand or co-catalyst in various reaction systems, facilitating transformations that would otherwise be challenging to achieve under standard conditions. For example, it has been employed in transition metal-catalyzed cross-coupling reactions, where it enhances reaction efficiency and selectivity. Such catalytic applications highlight the compound's versatility and its potential to streamline synthetic processes.
The environmental impact of using Diphenyldimethoxysilane has also been a subject of investigation. Studies have focused on developing greener synthetic routes that minimize waste generation and energy consumption. Researchers have explored solvent-free reactions and microwave-assisted synthesis techniques to improve efficiency while reducing environmental footprint. These efforts align with global initiatives to promote sustainable chemistry practices.
The future prospects of Diphenyldimethoxysilane are promising, with ongoing research expanding its applications across multiple disciplines. Advances in computational chemistry are enabling more precise predictions of its reactivity and behavior under different conditions, which will further enhance its utility in drug discovery and material design. Additionally, collaborations between academia and industry are fostering innovation by integrating cutting-edge technologies with traditional synthetic methodologies.
In conclusion, Diphenyldimethoxysilane (CAS No. 6843-66-9) is a multifaceted compound with broad applications in chemical research. Its unique structural features make it indispensable in material science, pharmaceutical development, organic synthesis, and catalysis. As research continues to uncover new possibilities for this versatile silane derivative, its role as a cornerstone material in advanced chemical applications is set to grow even further.
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