Cas no 24413-04-5 (Benzene,1-(chloromethyl)-4-(trimethoxysilyl)-)
Benzene,1-(chloromethyl)-4-(trimethoxysilyl)- Chemical and Physical Properties
Names and Identifiers
-
- Benzene,1-(chloromethyl)-4-(trimethoxysilyl)-
- 4-(CHLOROMETHYL)PHENYLTRIMETHOXYSILANE
- 4-Trimethoxysilylbenzyl chloride
- 4-CHLOROMETHYLPHENYLTRIMETHOXYSILANE
- S04350
- FT-0616731
- Silane, (4-(chloromethyl)phenyl)trimethoxy-
- p-chloromethylphenyltrimethoxysilane
- [4-(chloromethyl)phenyl]trimethoxysilane
- 24413-03-4
- 4-(Chloromethyl)Phenyltrimethoxysilane, Technical, 90%
- Benzene, 1-(chloromethyl)-4-(trimethoxysilyl)-
- NS00049830
- (p-(Chloromethyl)phenyl)trimethoxysilane
- 24413-04-5
- Silane, [4-(chloromethyl)phenyl]trimethoxy-
- MFCD00045269
- (p-chloromethyl)phenyltrimethoxy-silane
- SCHEMBL137014
- p-(Chloromethyl)phenyltrimethoxysilane
- ZXOFHTCCTUEJQJ-UHFFFAOYSA-N
- p-chloromethylphenyl trimethoxysilane
- EINECS 246-235-4
- (p-Chloromethylphenyl)trimethoxysilane
- (4-(chloromethyl)phenyl)trimethoxysilane
- 5NQ6H22HUK
- [4-(chloromethyl)phenyl]-trimethoxysilane
- 1-(Chloromethyl)-4-(trimethoxysilyl)benzene
- (p-chloromethyl)phenyltrimethoxysilane
- DTXSID7066984
- [p-(Chloromethyl)phenyl]trimethoxysilane
- p-(Trimethoxysilyl)benzyl chloride
- (p-Chloromethyl)phenyltrimethoxysilane, 95%
-
- MDL: MFCD00045269
- Inchi: 1S/C10H15ClO3Si/c1-12-15(13-2,14-3)10-6-4-9(8-11)5-7-10/h4-7H,8H2,1-3H3
- InChI Key: ZXOFHTCCTUEJQJ-UHFFFAOYSA-N
- SMILES: ClCC1C=CC(=CC=1)[Si](OC)(OC)OC
Computed Properties
- Exact Mass: 246.04800
- Monoisotopic Mass: 246.047899
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 15
- Rotatable Bond Count: 5
- Complexity: 171
- 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
- Surface Charge: 0
- Topological Polar Surface Area: 27.7
Experimental Properties
- Color/Form: colorless liquid
- Density: 1.12
- Melting Point: <0°C
- Boiling Point: 134 °C
- Flash Point: 83°C
- Refractive Index: 1.4965
- Water Partition Coefficient: Hydrolyzes in water.
- PSA: 27.69000
- LogP: 1.51050
- Sensitiveness: Moisture Sensitive
- Solubility: Not determined
Benzene,1-(chloromethyl)-4-(trimethoxysilyl)- 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:
P264Thoroughly clean after treatment
P280Wear protective gloves/Wear protective clothing/Wear protective goggles/Wear a protective mask
P305If it enters the eyes
P351Rinse carefully with water for a few minutes
P338Remove the contact lens(If any)And easy to operate,Continue flushing
P337If eye irritation persists
P313Obtain medical advice/care - Hazard Category Code: 36/37/38
- Safety Instruction: S26; S36/37/39
- HazardClass:8
- TSCA:Yes
- Risk Phrases:R36/37/38
- Safety Term:S26;S36/37/39;S45
- Storage Condition:Moisture Sensitive. Ambient temperatures.
Benzene,1-(chloromethyl)-4-(trimethoxysilyl)- 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%
Benzene,1-(chloromethyl)-4-(trimethoxysilyl)- Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| abcr | AB110963-25 g |
[4-(Chloromethyl)phenyl]trimethoxysilane, 95%; . |
24413-04-5 | 95% | 25 g |
€336.90 | 2023-07-20 | |
| abcr | AB110963-100 g |
[4-(Chloromethyl)phenyl]trimethoxysilane, 95%; . |
24413-04-5 | 95% | 100 g |
€1,026.90 | 2023-07-20 | |
| Fluorochem | S04350-25g |
4-(Chloromethyl)phenyltrimethoxysilane |
24413-04-5 | 25g |
£133.00 | 2022-02-28 | ||
| Fluorochem | S04350-100g |
4-(Chloromethyl)phenyltrimethoxysilane |
24413-04-5 | 100g |
£432.00 | 2022-02-28 | ||
| abcr | AB110963-25g |
[4-(Chloromethyl)phenyl]trimethoxysilane, 95%; . |
24413-04-5 | 95% | 25g |
€694.50 | 2025-02-19 | |
| abcr | AB110963-100g |
[4-(Chloromethyl)phenyl]trimethoxysilane, 95%; . |
24413-04-5 | 95% | 100g |
€1026.90 | 2024-06-11 | |
| 1PlusChem | 1P00C1UE-5g |
Silane, [4-(chloromethyl)phenyl]trimethoxy- |
24413-04-5 | 95% | 5g |
$87.00 | 2024-05-21 | |
| 1PlusChem | 1P00C1UE-25g |
Silane, [4-(chloromethyl)phenyl]trimethoxy- |
24413-04-5 | 95% | 25g |
$287.00 | 2024-05-21 | |
| A2B Chem LLC | AF61462-100g |
Silane, [4-(chloromethyl)phenyl]trimethoxy- |
24413-04-5 | 95% | 100g |
$1355.00 | 2023-12-31 | |
| A2B Chem LLC | AF61462-2kg |
Silane, [4-(chloromethyl)phenyl]trimethoxy- |
24413-04-5 | 95% | 2kg |
$6083.00 | 2023-12-31 |
Benzene,1-(chloromethyl)-4-(trimethoxysilyl)- Suppliers
Benzene,1-(chloromethyl)-4-(trimethoxysilyl)- Related Literature
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Weiwei He,Lifen Zhang,Bing Han,Liang Cheng,Nianchen Zhou,Zhuang Liu,Zhenping Cheng J. Mater. Chem. B 2013 1 3257
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Qiang Li,Lifen Zhang,Liangjiu Bai,Zhengbiao Zhang,Jian Zhu,Nianchen Zhou,Zhenping Cheng,Xiulin Zhu Soft Matter 2011 7 6958
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B?rbel Rückert,Andrew J. Hall,B?rje Sellergren J. Mater. Chem. 2002 12 2275
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Zhichao Ding,Changyou Chen,Yunlong Yu,Sissi de Beer J. Mater. Chem. B 2022 10 2430
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Nicole Herzer,Stephanie Hoeppener,Ulrich S. Schubert Chem. Commun. 2010 46 5634
Additional information on Benzene,1-(chloromethyl)-4-(trimethoxysilyl)-
Introduction to Benzene,1-(chloromethyl)-4-(trimethoxysilyl-) and Its Applications in Modern Chemical Research
Benzene,1-(chloromethyl)-4-(trimethoxysilyl-)CAS no. 24413-04-5, is a specialized organic compound that has garnered significant attention in the field of chemical and pharmaceutical research due to its unique structural properties and versatile reactivity. This compound, characterized by its chloromethyl and trimethoxysilyl functional groups, serves as a crucial intermediate in the synthesis of various high-value chemicals and materials. The presence of these distinct functional groups makes it an attractive candidate for applications ranging from polymer chemistry to drug development.
The chloromethyl group in Benzene,1-(chloromethyl)-4-(trimethoxysilyl-) introduces a high degree of reactivity, enabling the formation of carbon-carbon bonds through nucleophilic substitution reactions. This property is particularly valuable in organic synthesis, where it facilitates the construction of complex molecular architectures. On the other hand, the trimethoxysilyl group provides a means for surface modification and cross-linking, making this compound an excellent precursor for creating hybrid materials that combine organic and inorganic functionalities.
In recent years, Benzene,1-(chloromethyl)-4-(trimethoxysilyl-) has been extensively studied for its potential applications in the development of novel drug delivery systems. Researchers have leveraged its ability to undergo selective functionalization to create polymers with tailored properties that enhance drug solubility and bioavailability. For instance, studies have demonstrated its utility in designing biodegradable polymeric micelles capable of encapsulating hydrophobic drugs, thereby improving their delivery efficiency in therapeutic settings.
The compound's significance extends beyond pharmaceuticals into the realm of advanced materials science. The integration of the trimethoxysilyl group allows for the creation of silane-functionalized polymers that exhibit enhanced thermal stability and mechanical strength. These materials are particularly relevant in the fabrication of next-generation electronic devices, where high-performance polymers are essential for components such as flexible circuits and optoelectronic sensors. The ability to modify surfaces with this compound has also opened new avenues in nanotechnology, enabling the precise engineering of nanostructured surfaces for applications like anti-fouling coatings and biosensors.
Recent advancements in synthetic methodologies have further highlighted the versatility of Benzene,1-(chloromethyl)-4-(trimethoxysilyl-). Researchers have developed novel catalytic systems that enhance the efficiency of reactions involving this compound, reducing both reaction times and byproduct formation. These innovations are particularly important in large-scale industrial processes where cost-effectiveness and environmental sustainability are critical considerations. The optimization of synthetic routes has also enabled the production of derivatives with enhanced functionalities, broadening the scope of potential applications.
The intersection of chemistry and biology has led to intriguing studies on the biological activity of Benzene,1-(chloromethyl)-4-(trimethoxysilyl-). While primarily known as a synthetic intermediate, preliminary research suggests that certain derivatives may exhibit biological properties worthy of further investigation. For example, modifications to the chloromethyl group have been explored as a means to introduce bioactive molecules into polymer scaffolds designed for drug delivery. Such studies underscore the importance of interdisciplinary approaches in unlocking the full potential of this compound.
The future prospects for Benzene,1-(chloromethyl)-4-(trimethoxysilyl-) are promising, driven by ongoing research into its applications across multiple domains. As synthetic chemistry continues to evolve, new methodologies will likely emerge that further expand its utility. Additionally, advancements in computational chemistry and molecular modeling are expected to provide deeper insights into its reactivity and structural properties, enabling more targeted design of derivatives with specific functionalities.
In conclusion, Benzene,1-(chloromethyl)-4-(trimethoxysilyl-)CAS no. 24413-04-5 represents a cornerstone compound in modern chemical research. Its unique structural features and reactivity make it indispensable in various applications, from pharmaceuticals to advanced materials science. As research progresses, it is anticipated that this compound will continue to play a pivotal role in shaping the future of chemical innovation.
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