Cas no 109221-96-7 ((2-Phenoxy-phenyl)-hydrazine Hydrochloride)
(2-Phenoxy-phenyl)-hydrazine Hydrochloride Chemical and Physical Properties
Names and Identifiers
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- Hydrazine,(2-phenoxyphenyl)-, hydrochloride (1:1)
- (2-PHENOXYPHENYL)HYDRAZINE HYDROCHLORIDE,
- (2-Phenoxy-phenyl)-hydrazine, HCl
- (2-Phenoxy-phenyl)-hydrazin,Hydrochlorid
- (2-phenoxyphenyl)hydrazine
- (2-PHENOXY-PHENYL)-HYDRAZINE,HCL,hydrochloride
- BIO-FARMA BF000754
- (2-PHENOXY-PHENYL)-HYDRAZINE HYDROCHLORIDE
- 1-(2-PHENOXYPHENYL)HYDRAZINE HYDROCHLORIDE
- N'-(2-PHENOXY-PHENYL)-HYDRAZINIUM, CHLORIDE
- 109221-96-7
- (2-Phenoxyphenyl)HydrazineHydrochloride
- AB20850
- (2-Phenoxy-phenyl)-hydrazine hydrochloride, AldrichCPR
- (2-Phenoxyphenyl)Hydrazine Hydrochloride
- BS-25980
- EN300-264596
- MFCD04966823
- AKOS001475835
- CS-0206217
- (2-phenoxyphenyl)hydrazine;hydrochloride
- SCHEMBL4382625
- G24165
- (2-Phenoxy-phenyl)-hydrazine Hydrochloride
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- MDL： MFCD04966823
- Inchi： 1S/C12H12N2O.ClH/c13-14-11-8-4-5-9-12(11)15-10-6-2-1-3-7-10;/h1-9,14H,13H2;1H
- InChI Key： DJVCMGYLUIMOTN-UHFFFAOYSA-N
- SMILES： Cl.O(C1C=CC=CC=1)C1C=CC=CC=1NN
Computed Properties
- Exact Mass: 236.07200
- Monoisotopic Mass: 236.0716407g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 16
- Rotatable Bond Count: 3
- Complexity: 181
- Covalently-Bonded Unit Count: 2
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 47.3?2
Experimental Properties
- PSA: 47.28000
- LogP: 4.33980
(2-Phenoxy-phenyl)-hydrazine Hydrochloride Customs Data
- HS CODE：2928000090
- Customs Data：
China Customs Code:
2928000090Overview:
2928000090 Other hydrazine(Hydrazine)And chlorhexidine(hydroxylamine)Organic derivatives of.Regulatory conditions:nothing.VAT:17.0%.Tax refund rate:9.0%.MFN tariff:6.5%.general tariff:20.0%
Declaration elements:
Product Name, component content, use to
Summary:
2928000090 other organic derivatives of hydrazine or of hydroxylamine VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%
(2-Phenoxy-phenyl)-hydrazine Hydrochloride Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A250001738-1g |
(2-Phenoxyphenyl)hydrazine hydrochloride |
109221-96-7 | 95% | 1g |
$303.60 | 2023-09-04 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | P165875-1g |
(2-Phenoxy-phenyl)-hydrazine hydrochloride |
109221-96-7 | 1g |
￥2,344.00 | 2021-05-24 | ||
| JIE DA WEI （ SHANG HAI ） YI YAO KE JI FA ZHAN Co., Ltd. | 20R0238S-1g |
(2-Phenoxy-phenyl)-hydrazine hydrochloride |
109221-96-7 | 96% | 1g |
2374.52CNY | 2021-05-08 | |
| JIE DA WEI （ SHANG HAI ） YI YAO KE JI FA ZHAN Co., Ltd. | 20R0238S-5g |
(2-Phenoxy-phenyl)-hydrazine hydrochloride |
109221-96-7 | 96% | 5g |
8463.46CNY | 2021-05-08 | |
| JIE DA WEI （ SHANG HAI ） YI YAO KE JI FA ZHAN Co., Ltd. | 20R0238S-500mg |
(2-Phenoxy-phenyl)-hydrazine hydrochloride |
109221-96-7 | 96% | 500mg |
1611.28CNY | 2021-05-08 | |
| JIE DA WEI （ SHANG HAI ） YI YAO KE JI FA ZHAN Co., Ltd. | 20R0238S-250mg |
(2-Phenoxy-phenyl)-hydrazine hydrochloride |
109221-96-7 | 96% | 250mg |
1229.66CNY | 2021-05-08 | |
| JIE DA WEI （ SHANG HAI ） YI YAO KE JI FA ZHAN Co., Ltd. | 20R0238S-100mg |
(2-Phenoxy-phenyl)-hydrazine hydrochloride |
109221-96-7 | 96% | 100mg |
1060.05CNY | 2021-05-08 | |
| JIE DA WEI （ SHANG HAI ） YI YAO KE JI FA ZHAN Co., Ltd. | 20R0238S-50mg |
(2-Phenoxy-phenyl)-hydrazine hydrochloride |
109221-96-7 | 96% | 50mg |
924.37CNY | 2021-05-08 | |
| abcr | AB536375-1 g |
(2-Phenoxy-phenyl)-hydrazine hydrochloride |
109221-96-7 | 1g |
€534.00 | 2023-04-14 | ||
| TRC | P399723-50mg |
(2-Phenoxy-phenyl)-hydrazine Hydrochloride |
109221-96-7 | 50mg |
$ 50.00 | 2022-06-03 |
(2-Phenoxy-phenyl)-hydrazine Hydrochloride Related Literature
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P. K. Wawrzyniak,M. T. P. Beerepoot,H. J. M. de Groot,F. Buda Phys. Chem. Chem. Phys., 2011,13, 10270-10279
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Attila N. Lázár,Derek Clarke,Helen Adams,Abdur Razzaque Akanda,Sylvia Szabo,Robert J. Nicholls,Zoe Matthews,Dilruba Begum,Abul Fazal M. Saleh,Md. Anwarul Abedin,Andres Payo,Peter Kim Streatfield,Craig Hutton,M. Shahjahan Mondal,Abu Zofar Md. Moslehuddin Environ. Sci.: Processes Impacts, 2015,17, 1018-1031
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Huabin Zhang,Shaowu Du CrystEngComm, 2014,16, 4059-4068
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Jingquan Liu,Huiyun Liu,Zhongfan Jia,Volga Bulmus,Thomas P. Davis Chem. Commun., 2008, 6582-6584
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Soumaya Khlifi,Gregory Mouille,Jonathan Farjon Anal. Methods, 2017,9, 2328-2333
Additional information on (2-Phenoxy-phenyl)-hydrazine Hydrochloride
Introduction to (2-Phenoxy-phenyl)-hydrazine Hydrochloride (CAS No. 109221-96-7)
The compound (2-Phenoxy-phenyl)-hydrazine Hydrochloride, identified by the CAS registry number CAS No. 109221-96-7, is a significant chemical entity with diverse applications in various scientific and industrial domains. This compound has garnered attention due to its unique chemical properties and potential uses in fields such as pharmaceuticals, agrochemicals, and material sciences.
Recent advancements in chemical synthesis and characterization techniques have enabled researchers to delve deeper into the properties of (2-Phenoxy-phenyl)-hydrazine Hydrochloride. Studies have highlighted its role as a versatile building block in organic synthesis, particularly in the development of bioactive molecules with potential therapeutic applications.
The molecular structure of (2-Phenoxy-phenyl)-hydrazine Hydrochloride comprises a phenoxy group attached to a phenyl ring, which is further connected to a hydrazine moiety. This arrangement imparts the compound with unique electronic and steric properties, making it an attractive candidate for various chemical transformations.
One of the most notable applications of this compound is its use as an intermediate in the synthesis of heterocyclic compounds, which are crucial components of many drugs and agrochemicals. Recent research has demonstrated its effectiveness in forming fused ring systems, which are essential for achieving desired pharmacokinetic profiles in drug candidates.
In addition to its synthetic utility, (2-Phenoxy-phenyl)-hydrazine Hydrochloride has been explored for its potential in catalytic processes. Its ability to act as a ligand in transition metal-catalyzed reactions has opened new avenues for asymmetric synthesis and enantioselective catalysis.
The physical properties of this compound, including its melting point, solubility, and stability under various conditions, have been extensively studied. These studies have provided valuable insights into its handling and storage requirements, ensuring safe and efficient use in laboratory settings.
Recent collaborative efforts between academic institutions and industry have led to the development of novel synthetic routes for (2-Phenoxy-phenyl)-hydrazine Hydrochloride. These methods not only enhance the scalability of production but also improve the overall sustainability of the manufacturing process.
The compound's role in drug discovery has been further bolstered by its ability to modulate key biological targets. Preclinical studies have shown promise in its potential application as an anti-inflammatory agent, with research indicating significant reductions in inflammatory markers in experimental models.
Moreover, the integration of computational chemistry techniques has enabled researchers to predict the compound's interactions with various biological systems more accurately. This computational approach has significantly accelerated the drug discovery process by identifying potential leads more efficiently.
In conclusion, (2-Phenoxy-phenyl)-hydrazine Hydrochloride stands as a testament to the continuous evolution of chemical science. Its versatility and adaptability make it an invaluable tool across multiple disciplines, paving the way for innovative solutions to complex scientific challenges.
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