Cas no 175135-06-5 (3,5-Dichloro-4-(2-chloro-4-nitrophenoxy)benzene-1-sulfonyl chloride)
3,5-Dichloro-4-(2-chloro-4-nitrophenoxy)benzene-1-sulfonyl chloride Chemical and Physical Properties
Names and Identifiers
-
- 3,5-Dichloro-4-(2-chloro-4-nitrophenoxy)benzene-1-sulfonyl chloride
- 3,5-DICHLORO-4-(2-CHLORO-4-NITROPHENOXY)BENZENE-1-SULPHONYL CHLORIDE
- 3,5-dichloro-4-(2-chloro-4-nitrophenoxy)benzenesulfonyl chloride
- Benzenesulfonylchloride, 3,5-dichloro-4-(2-chloro-4-nitrophenoxy)-
- BUTTPARK 97\12-02
- 4-(2-CHLORO-4-NITROPHENOXY)-3,5-DICHLOROBENZENESULFONYL CHLORIDE
- SCHEMBL1019827
- 175135-06-5
- AKOS015912021
- MS-21960
- Benzenesulfonyl chloride, 3,5-dichloro-4-(2-chloro-4-nitrophenoxy)-
- 4-(2-chloro-4-nitrophenoxy)-3,5-dichloro-benzenesulfonyl chloride
- EN300-18537106
- FT-0614539
- DTXSID40378997
- MFCD00052029
- 3,5-DICHLORO-4-(2-CHLORO-4-NITROPHENOXY)BENZENE-1-SULFONYLCHLORIDE
- YNPAAILIMIGQIH-UHFFFAOYSA-N
- J-511284
-
- MDL: MFCD00052029
- Inchi: 1S/C12H5Cl4NO5S/c13-8-3-6(17(18)19)1-2-11(8)22-12-9(14)4-7(5-10(12)15)23(16,20)21/h1-5H
- InChI Key: YNPAAILIMIGQIH-UHFFFAOYSA-N
- SMILES: ClC1C=C(C=C(C=1OC1C=CC(=CC=1Cl)[N+](=O)[O-])Cl)S(=O)(=O)Cl
Computed Properties
- Exact Mass: 414.86400
- Monoisotopic Mass: 414.864254g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 23
- Rotatable Bond Count: 3
- Complexity: 525
- 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: 5.2
- Topological Polar Surface Area: 97.6?2
Experimental Properties
- Density: 1.706
- Melting Point: 159 °C
- Boiling Point: 455.6°Cat760mmHg
- Flash Point: 229.4°C
- Refractive Index: 1.633
- PSA: 97.57000
- LogP: 6.87880
3,5-Dichloro-4-(2-chloro-4-nitrophenoxy)benzene-1-sulfonyl chloride Security Information
- Hazardous Material transportation number:UN 3261
- Hazard Category Code: 34
- Safety Instruction: S26; S36/37/39
- Risk Phrases:R34
- Safety Term:S26-36/37/39
3,5-Dichloro-4-(2-chloro-4-nitrophenoxy)benzene-1-sulfonyl chloride Customs Data
- HS CODE:2909309090
- Customs Data:
China Customs Code:
2909309090Overview:
2909309090 Other aromatic ethers and their halogenated derivatives\sulfonation\Nitrated derivative(Including nitrosative derivatives).Regulatory conditions:nothing.VAT:17.0%.Tax refund rate:9.0%.MFN tariff:5.5%.general tariff:30.0%
Declaration elements:
Product Name, component content, use to
Summary:
2909309090 other aromatic ethers and their halogenated, sulphonated, nitrated or nitrosated derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%
3,5-Dichloro-4-(2-chloro-4-nitrophenoxy)benzene-1-sulfonyl chloride Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| abcr | AB145597-1 g |
3,5-Dichloro-4-(2-chloro-4-nitrophenoxy)benzene-1-sulfonyl chloride; 95% |
175135-06-5 | 1 g |
€57.30 | 2023-07-20 | ||
| abcr | AB145597-10 g |
3,5-Dichloro-4-(2-chloro-4-nitrophenoxy)benzene-1-sulfonyl chloride; 95% |
175135-06-5 | 10 g |
€419.70 | 2023-07-20 | ||
| Key Organics Ltd | MS-21960-1g |
3,5-dichloro-4-(2-chloro-4-nitrophenoxy)benzene-1-sulfonyl chloride |
175135-06-5 | >97% | 1g |
£51.00 | 2025-02-09 | |
| Key Organics Ltd | MS-21960-10g |
3,5-dichloro-4-(2-chloro-4-nitrophenoxy)benzene-1-sulfonyl chloride |
175135-06-5 | >97% | 10g |
£386.00 | 2025-02-09 | |
| A2B Chem LLC | AA93336-1g |
Benzenesulfonyl chloride, 3,5-dichloro-4-(2-chloro-4-nitrophenoxy)- |
175135-06-5 | 95% | 1g |
$163.00 | 2024-04-20 | |
| A2B Chem LLC | AA93336-5g |
Benzenesulfonyl chloride, 3,5-dichloro-4-(2-chloro-4-nitrophenoxy)- |
175135-06-5 | 95% | 5g |
$495.00 | 2024-04-20 | |
| eNovation Chemicals LLC | Y1233731-1g |
Benzenesulfonyl chloride, 3,5-dichloro-4-(2-chloro-4-nitrophenoxy)- |
175135-06-5 | 95% | 1g |
$290 | 2025-02-22 | |
| eNovation Chemicals LLC | Y1233731-5g |
Benzenesulfonyl chloride, 3,5-dichloro-4-(2-chloro-4-nitrophenoxy)- |
175135-06-5 | 95% | 5g |
$775 | 2025-02-22 | |
| eNovation Chemicals LLC | Y1233731-1g |
Benzenesulfonyl chloride, 3,5-dichloro-4-(2-chloro-4-nitrophenoxy)- |
175135-06-5 | 95% | 1g |
$290 | 2025-02-21 | |
| eNovation Chemicals LLC | Y1233731-5g |
Benzenesulfonyl chloride, 3,5-dichloro-4-(2-chloro-4-nitrophenoxy)- |
175135-06-5 | 95% | 5g |
$775 | 2025-02-21 |
3,5-Dichloro-4-(2-chloro-4-nitrophenoxy)benzene-1-sulfonyl chloride Suppliers
3,5-Dichloro-4-(2-chloro-4-nitrophenoxy)benzene-1-sulfonyl chloride Related Literature
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Guiying Zhang,Maosheng Cheng,Yanni Li,Keliang Liu,Lifeng Cai Chem. Commun., 2013,49, 11086-11088
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Eric Besson,Stéphane Gastaldi,Emily Bloch,Selma Aslan,Hakim Karoui,Olivier Ouari,Micael Hardy Analyst, 2019,144, 4194-4203
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Long Deng,Qian Zou,Biao Liu,Wenhui Ye,Chengfei Zhuo,Li Chen,Ze-Yuan Deng,Ya-Wei Fan,Jing Li Food Funct., 2018,9, 4234-4245
Additional information on 3,5-Dichloro-4-(2-chloro-4-nitrophenoxy)benzene-1-sulfonyl chloride
Comprehensive Overview of 3,5-Dichloro-4-(2-chloro-4-nitrophenoxy)benzene-1-sulfonyl chloride (CAS No. 175135-06-5)
3,5-Dichloro-4-(2-chloro-4-nitrophenoxy)benzene-1-sulfonyl chloride (CAS No. 175135-06-5) is a specialized organic compound widely utilized in advanced chemical synthesis and pharmaceutical research. This compound belongs to the family of sulfonyl chlorides, which are known for their reactivity and versatility in forming sulfonamides, sulfonate esters, and other derivatives. The presence of multiple chloro and nitro substituents enhances its electrophilic character, making it a valuable intermediate in the development of agrochemicals, dyes, and bioactive molecules.
In recent years, the demand for high-purity sulfonyl chlorides has surged due to their critical role in drug discovery and material science. Researchers frequently search for "synthesis of sulfonyl chloride derivatives" or "applications of 3,5-dichloro-4-substituted benzene sulfonyl chlorides," reflecting the growing interest in this chemical class. The compound's unique structure, featuring a nitrophenoxy group, also contributes to its utility in designing photoactive materials and catalysts.
From an industrial perspective, 3,5-Dichloro-4-(2-chloro-4-nitrophenoxy)benzene-1-sulfonyl chloride is often synthesized through controlled chlorination and nitration reactions. Its CAS No. 175135-06-5 serves as a key identifier in regulatory and safety documentation, ensuring compliance with global chemical standards. Environmental and sustainability concerns have also driven innovations in its production, with a focus on "green chemistry approaches for sulfonyl chloride synthesis" gaining traction in academic and industrial forums.
The compound's stability under ambient conditions and solubility in organic solvents like dichloromethane and tetrahydrofuran make it a preferred choice for laboratory-scale reactions. Analytical techniques such as HPLC, NMR, and mass spectrometry are routinely employed to verify its purity and structural integrity. These methods align with the broader trend of "quality control in specialty chemicals," a topic frequently explored in peer-reviewed journals and technical conferences.
Emerging applications of 3,5-Dichloro-4-(2-chloro-4-nitrophenoxy)benzene-1-sulfonyl chloride include its use in polymer modification and surface functionalization. For instance, its reactive sulfonyl chloride group can be grafted onto polymeric matrices to impart specific properties like hydrophobicity or adhesion. Such innovations resonate with searches like "functionalized polymers for industrial coatings" or "advanced materials for electronics," highlighting its cross-disciplinary relevance.
In summary, 3,5-Dichloro-4-(2-chloro-4-nitrophenoxy)benzene-1-sulfonyl chloride (CAS No. 175135-06-5) exemplifies the intersection of synthetic chemistry and applied science. Its multifaceted applications, coupled with rigorous research into sustainable production methods, position it as a compound of enduring significance in both academic and industrial settings.
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