Cas no 4478-92-6 (1-phenylethyl isothiocyanate)
1-phenylethyl isothiocyanate Chemical and Physical Properties
Names and Identifiers
-
- alpha-Methylbenzyl isothiocyanate
- DL-alpha-Methylbenzyl isothiocyanate
- (+/-)-1-Phenylethyl isothiocyanate
- (±)-1-Phenylethyl isothiocyanate
- 1-phenylethyl isothiocyanate
- Benzene,(1-isothiocyanatoethyl)-
- (1-isothiocyanato-ethyl)-benzene
- (n)-1-phenylethyl isothiocyanate
- 1-Phenethylisothiocyanate
- Benzene, (1-isothiocyanatoethyl)-, (A+/-)-
- AKOS000101073
- (r)-(-)-1-phenylethyl isothiocyanate
- VS-03392
- FT-0608258
- DL-.alpha.-Methylbenzyl isothiocyanate
- D-.alpha.-Methylbenzyl isothiocyanate
- (1-Isothiocyanatoethyl)benzene
- 1-isothiocyanatoethylbenzene
- A821255
- Isothiocyanic acid, (.alpha.-methylbenzyl) ester
- (1-Isothiocyanatoethyl)benzene #
- L-alpha-Methylbenzyl isothiocyanate
- 1-PHENYLETHYLISOTHIOCYANATE
- dl-A-Methylbenzyl isothiocyanate
- FT-0608257
- FT-0694119
- alpha-methyl benzyl isothiocyanate
- 4478-92-6
- (?)-1-Phenylethyl isothiocyanate
- AKOS017269392
- PD138984
- 32393-32-1
- Benzene,[(1R)-1-isothiocyanatoethyl]-
- EN300-43612
- SCHEMBL156959
- ZAA27744
- NSC221236
- L-.alpha.-Methylbenzyl isothiocyanate
- MFCD00022061
- NSC-221236
- Benzene, (1-isothiocyanatoethyl)-
- HY-131718
- NSC 221236
- WLN: SCNY1&R
- BDBM50073653
- dl-alpha-methylbenzylisothiocyanate
- .alpha.-Methylbenzyl isothiocyanate
- CS-0139291
- ISOTHIOCYANIC ACID, (alpha-METHYLBENZYL) ESTER
- CHEMBL2251720
- FT-0720875
- Z57358351
- Dimethylmethylsuccinate
- ( inverted exclamation markA)-1-Phenylethyl isothiocyanate
- DTXSID90947112
- STK397869
- Benzene, (1-isothiocyanatoethyl)-, (+/-)-
- G86037
- BBL012571
- DB-070591
-
- MDL: MFCD00022061
- Inchi: 1S/C9H9NS/c1-8(10-7-11)9-5-3-2-4-6-9/h2-6,8H,1H3
- InChI Key: QQCJPTVZIZVKEZ-UHFFFAOYSA-N
- SMILES: S=C=NC(C)C1C=CC=CC=1
- BRN: 2207685
Computed Properties
- Exact Mass: 163.04600
- Monoisotopic Mass: 163.046
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 11
- Rotatable Bond Count: 2
- Complexity: 155
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 1
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Surface Charge: 0
- Tautomer Count: nothing
- XLogP3: nothing
- Topological Polar Surface Area: 44.4A^2
Experimental Properties
- Color/Form: Yellow to brown liquid
- Density: 1,06 g/cm3
- Boiling Point: 132 °C
- Flash Point: 103°C
- Refractive Index: 1.5810
- PSA: 44.45000
- LogP: 2.85040
- Sensitiveness: Moisture Sensitive
- Solubility: hydrolysis
1-phenylethyl isothiocyanate Security Information
- Hazard Statement: Harmful
- Hazardous Material transportation number:UN 2810
- Hazard Category Code: 23/24/25-36/37/38
- Safety Instruction: S26-S36/37/39
- RTECS:NX8800000
- HazardClass:8
- PackingGroup:III
- Safety Term:S26;S36/37/39
- Packing Group:III
- Packing Group:III
- Risk Phrases:R20/21/22; R36/37/38
1-phenylethyl isothiocyanate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | B521790-250mg |
1-phenylethyl isothiocyanate |
4478-92-6 | 250mg |
$ 50.00 | 2022-06-07 | ||
| TRC | B521790-500mg |
1-phenylethyl isothiocyanate |
4478-92-6 | 500mg |
$ 65.00 | 2022-06-07 | ||
| TRC | B521790-2.5g |
1-phenylethyl isothiocyanate |
4478-92-6 | 2.5g |
$ 80.00 | 2022-06-07 | ||
| Fluorochem | 009523-1g |
DL-Methylbenzylisothiocyanate |
4478-92-6 | 98% | 1g |
£11.00 | 2022-03-01 | |
| Fluorochem | 009523-5g |
DL-Methylbenzylisothiocyanate |
4478-92-6 | 98% | 5g |
£18.00 | 2022-03-01 | |
| Fluorochem | 009523-25g |
DL-Methylbenzylisothiocyanate |
4478-92-6 | 98% | 25g |
£78.00 | 2022-03-01 | |
| Apollo Scientific | OR28863-5g |
1-Phenylethyl isothiocyanate |
4478-92-6 | 5g |
£80.00 | 2025-02-19 | ||
| abcr | AB125869-25 g |
(±)-1-Phenylethyl isothiocyanate, 97%; . |
4478-92-6 | 97% | 25 g |
€149.50 | 2023-07-20 | |
| Key Organics Ltd | VS-03392-0.5G |
(1-isothiocyanatoethyl)benzene |
4478-92-6 | >90% | 0.5g |
£175.00 | 2025-02-08 | |
| Key Organics Ltd | VS-03392-1G |
(1-isothiocyanatoethyl)benzene |
4478-92-6 | >90% | 1g |
£287.00 | 2025-02-08 |
1-phenylethyl isothiocyanate Related Literature
-
Marek Tobiszewski,Jacek Namie?nik,Francisco Pena-Pereira Green Chem. 2017 19 5911
Additional information on 1-phenylethyl isothiocyanate
Comprehensive Guide to 1-Phenylethyl Isothiocyanate (CAS No. 4478-92-6): Properties, Applications, and Research Insights
1-Phenylethyl isothiocyanate (CAS No. 4478-92-6) is an organosulfur compound belonging to the isothiocyanate family. This compound has garnered significant attention in recent years due to its unique chemical properties and potential applications in various fields, including pharmaceutical research, flavor chemistry, and agricultural science. With the increasing demand for bioactive compounds in nutraceuticals and functional foods, researchers are exploring the multifaceted roles of 1-phenylethyl isothiocyanate in human health and industrial processes.
The molecular structure of 1-phenylethyl isothiocyanate features a phenyl group attached to an ethyl chain terminating in an isothiocyanate functional group (-N=C=S). This configuration contributes to its volatile nature and pungent aroma, characteristics that make it valuable in aroma profiling and food flavoring applications. Recent studies have highlighted its potential as a natural preservative, aligning with the growing consumer preference for clean-label ingredients in the food industry.
In biomedical research, 1-phenylethyl isothiocyanate has shown promise due to its bioactive properties. Scientists are investigating its potential role in cellular signaling pathways and its interaction with enzymatic processes. These studies are particularly relevant in the context of nutraceutical development, where natural compounds are being explored for their health benefits. The compound's mechanism of action and structure-activity relationship are currently subjects of intense research in pharmacology and biochemistry.
The synthesis of 1-phenylethyl isothiocyanate typically involves the reaction of 1-phenylethylamine with carbon disulfide, followed by treatment with an alkylating agent. This process yields a compound with high purity, suitable for various research and industrial applications. Analytical techniques such as gas chromatography-mass spectrometry (GC-MS) and nuclear magnetic resonance (NMR) spectroscopy are commonly employed to characterize and verify the compound's structure and purity.
From an industrial perspective, 1-phenylethyl isothiocyanate finds applications in the flavor and fragrance industry. Its distinct sensory profile makes it valuable for creating complex flavor compositions, particularly in specialty food products and beverages. The compound's volatility and stability under various processing conditions make it suitable for thermal food processing applications, addressing key challenges in food technology.
Environmental considerations regarding 1-phenylethyl isothiocyanate have also emerged as an important research area. Scientists are studying its biodegradation pathways and environmental fate to ensure sustainable use in industrial applications. This aligns with the global push toward green chemistry principles and the development of eco-friendly chemical processes.
In the realm of analytical chemistry, 1-phenylethyl isothiocyanate serves as a valuable reference standard and derivatization agent. Its well-characterized properties make it useful for method development and instrument calibration in various chromatographic techniques. Researchers are continually exploring new applications for this compound in analytical method validation and quality control procedures.
The safety profile of 1-phenylethyl isothiocyanate has been extensively studied, with research focusing on its toxicological properties and exposure limits. Proper handling procedures and personal protective equipment are recommended when working with this compound in laboratory settings. These safety considerations are particularly important in industrial hygiene and occupational health contexts.
Looking toward the future, research on 1-phenylethyl isothiocyanate continues to expand, with particular interest in its potential applications in sustainable agriculture as a natural pesticide alternative. The compound's mode of action against various pests and its environmental compatibility make it an attractive subject for agrochemical research and development.
In conclusion, 1-phenylethyl isothiocyanate (CAS No. 4478-92-6) represents a versatile compound with diverse applications across multiple scientific disciplines. Its unique chemical properties, combined with growing interest in bioactive natural products, position it as an important subject for ongoing research and development. As scientific understanding of this compound deepens, new applications and benefits are likely to emerge, further solidifying its importance in chemical research and industrial applications.
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