Cas no 24596-18-7 (4-Chloro-2,6-dimethylaniline)
4-Chloro-2,6-dimethylaniline Chemical and Physical Properties
Names and Identifiers
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- 4-Chloro-2,6-dimethylaniline
- 4-Chloro-2,6-dimethylbenzenamine
- 4-Chloro-2,6-xylidine
- 2,6-dimethyl-4-chloroaniline
- 4-Chlor-2,6-dimethyl-anilin
- 4-chloro-2,6-dimethyl-aniline
- 4-chloro-2,6-dimethylphenylamine
- 5-Chlor-2-amino-m-xylol
- PHARMABRIDGE P-1739
- Benzenamine, 4-chloro-2,6-dimethyl-
- A5052
- MFCD01076576
- 4-Chloro-2,6-dimethyl-phenylamine
- JCLZLZKUISPXDC-UHFFFAOYSA-N
- CCG-302552
- SCHEMBL203946
- DTXSID00408047
- AKOS015842433
- SB76560
- AS-18849
- 24596-18-7
- 4-Chlor-2,6-dimethylanilin
- CS-0013262
- FT-0638438
- Z1511494953
- EN300-117114
- SY022852
- DB-046498
- STL450370
-
- MDL: MFCD01076576
- Inchi: 1S/C8H10ClN/c1-5-3-7(9)4-6(2)8(5)10/h3-4H,10H2,1-2H3
- InChI Key: JCLZLZKUISPXDC-UHFFFAOYSA-N
- SMILES: ClC1C=C(C)C(=C(C)C=1)N
Computed Properties
- Exact Mass: 155.05000
- Monoisotopic Mass: 155.05
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 10
- Rotatable Bond Count: 0
- Complexity: 104
- 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
- Tautomer Count: nothing
- XLogP3: 2.6
- Topological Polar Surface Area: 26A^2
Experimental Properties
- Color/Form: solid
- Density: 1.142
- Melting Point: 45-50°C
- Boiling Point: 260.6 ℃ at 760 mmHg
- Flash Point: 111.4°C
- Refractive Index: 1.575
- Water Partition Coefficient: Slightly soluble in water.
- PSA: 26.02000
- LogP: 3.12020
- Solubility: Not determined
4-Chloro-2,6-dimethylaniline Security Information
- Hazardous Material transportation number:2811
- WGK Germany:3
- Hazard Category Code: 23/24/25-36/37/38
- Safety Instruction: S23-S36/37/39-S45
-
Hazardous Material Identification:
- Risk Phrases:R23/24/25
4-Chloro-2,6-dimethylaniline Customs Data
- HS CODE:2921430090
- Customs Data:
China Customs Code:
2921430090Overview:
2921430090 Toluidine and its derivatives and their salts. VAT:17.0% Tax refund rate:9.0% Regulatory conditions:nothing MFN tariff:6.5% general tariff:30.0%
Declaration elements:
Product Name, component content, use to, Evidence document and number of origin(example Certificate of origin attached, Originating in the European Union
Summary:
HS:2921430090 toluidines and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%
4-Chloro-2,6-dimethylaniline Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | C424130-1g |
4-Chloro-2,6-xylidine |
24596-18-7 | 1g |
$ 125.00 | 2022-06-06 | ||
| TRC | C424130-10g |
4-Chloro-2,6-xylidine |
24596-18-7 | 10g |
$ 315.00 | 2022-06-06 | ||
| Fluorochem | 219764-10g |
4-Chloro-2,6-dimethylaniline |
24596-18-7 | 98% | 10g |
£153.00 | 2022-03-01 | |
| Fluorochem | 219764-100g |
4-Chloro-2,6-dimethylaniline |
24596-18-7 | 98% | 100g |
£600.00 | 2022-03-01 | |
| Apollo Scientific | OR61435-250mg |
4-Chloro-2,6-dimethylaniline |
24596-18-7 | 98% | 250mg |
£15.00 | 2025-03-21 | |
| Ambeed | A125101-250mg |
4-Chloro-2,6-dimethylaniline |
24596-18-7 | 98% | 250mg |
$19.0 | 2024-08-03 | |
| Ambeed | A125101-1g |
4-Chloro-2,6-dimethylaniline |
24596-18-7 | 98% | 1g |
$24.0 | 2024-08-03 | |
| Ambeed | A125101-5g |
4-Chloro-2,6-dimethylaniline |
24596-18-7 | 98% | 5g |
$69.0 | 2024-08-03 | |
| abcr | AB132360-100 g |
4-Chloro-2,6-dimethylaniline, 98%; . |
24596-18-7 | 98% | 100g |
€654.00 | 2023-05-10 | |
| abcr | AB132360-5 g |
4-Chloro-2,6-dimethylaniline, 98%; . |
24596-18-7 | 98% | 5g |
€96.40 | 2023-05-10 |
4-Chloro-2,6-dimethylaniline Suppliers
4-Chloro-2,6-dimethylaniline Related Literature
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1. 606. Molecular rearrangements. Part II. 2 : 6-Disubstituted N-chloroacetanilidesC. Beard,W. J. Hickinbottom J. Chem. Soc. 1958 2982
Additional information on 4-Chloro-2,6-dimethylaniline
Comprehensive Overview of 4-Chloro-2,6-dimethylaniline (CAS No. 24596-18-7): Properties, Applications, and Industry Insights
4-Chloro-2,6-dimethylaniline (CAS No. 24596-18-7) is a specialized organic compound widely recognized for its role in fine chemical synthesis. This aromatic amine, characterized by its chloro and methyl substituents, serves as a critical intermediate in pharmaceuticals, agrochemicals, and dye manufacturing. With the growing demand for high-purity intermediates, this compound has garnered significant attention in research and industrial applications.
The molecular structure of 4-Chloro-2,6-dimethylaniline features a benzene ring substituted with a chlorine atom at the 4-position and methyl groups at the 2- and 6-positions. This unique arrangement enhances its reactivity in electrophilic substitution reactions, making it valuable for synthesizing complex molecules. Researchers frequently explore its derivatization potential, particularly in developing azo dyes and pharmaceutical precursors.
In the pharmaceutical sector, 4-Chloro-2,6-dimethylaniline is employed in the synthesis of active pharmaceutical ingredients (APIs). Its role in constructing heterocyclic frameworks aligns with trends in targeted drug discovery, a hot topic in 2024 due to advancements in AI-driven molecular design. The compound’s stability under mild conditions also makes it suitable for green chemistry applications, addressing the industry’s shift toward sustainable synthesis.
Agrochemical applications leverage 4-Chloro-2,6-dimethylaniline as a precursor for crop protection agents. With rising global focus on food security and precision agriculture, demand for efficient intermediates like this compound continues to grow. Its derivatives contribute to herbicides and fungicides with improved environmental profiles, reflecting regulatory pressures for low-residue formulations.
From a technical perspective, the compound’s physicochemical properties—including a melting point of 60–62°C and moderate solubility in organic solvents—facilitate its handling in industrial processes. Analytical methods such as HPLC and GC-MS are commonly used for purity verification, ensuring compliance with Good Manufacturing Practices (GMP). These quality control measures resonate with current discussions on supply chain transparency in chemical procurement.
Market trends indicate increasing R&D investments in custom synthesis of 4-Chloro-2,6-dimethylaniline derivatives. Patent analyses reveal applications in electronic materials, particularly for organic semiconductors, aligning with the booming flexible electronics sector. This interdisciplinary relevance underscores the compound’s versatility beyond traditional uses.
Environmental and safety considerations for CAS 24596-18-7 emphasize proper waste management and worker protection. While not classified as hazardous under standard protocols, its handling requires adherence to REACH and OSHA guidelines. These aspects are frequently searched by EHS professionals, reflecting broader corporate commitments to ESG (Environmental, Social, and Governance) principles.
In conclusion, 4-Chloro-2,6-dimethylaniline remains a pivotal building block in modern chemistry. Its intersection with cutting-edge technologies and sustainability goals positions it as a compound of enduring relevance. Future research may explore its potential in bioconjugation chemistry or catalysis, further expanding its industrial footprint.
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