Cas no 14092-04-7 (1-Propenylmagnesium bromide)
1-Propenylmagnesium bromide Chemical and Physical Properties
Names and Identifiers
-
- (E)-Prop-1-en-1-ylmagnesium bromide
- 1-PROPENYLMAGNESIUM BROMIDE
- 1-Propenylmagnesium bromide, 0.5 M solution in THF, SpcSeal
- Magnesium,bromo-1-propenyl- (9CI)
- (prop-1-enyl)magnesium bromide
- 1-Propenylbromomagnesium
- 1-Propenylmagnesium bromide solution
- 1-Propenylmagnesium bromide,0.5M solution in THF,AcroSeal
- 2-propenylmagnesiumbromide
- Bromo(1-propenyl) magnesium
- prop-1-en-1-ylmagnesium bromide
- Propenylmagnesiumbromide
- 1-Propenylmagnesium bromide 0.5M solution in THF
- 1-PropenylMagnesiuM broMide solution 0.5 M in THF
- Propenylmagnesium bromide
- 1-Propenylmagnesium bromide, 0.5M solution in THF, AcroSeal
- 1-Propenyl Magnesium Bromide
- (Z-propenylmagnesium)bromide
- Magnesium, bromo-(1Z)-1-propenyl-
- (E)-prop-1-enylmagnesium bromide
- propenyl magnesium bromide
- trans-1-propenyl-magnesium bromide
- SCHEMBL262691
- MFCD00209610
- 13154-14-8
- HHNLJRLNDSEYOX-UHFFFAOYSA-M
- (e)-propenylmagnesium bromide
- Magnesium, bromo-1-propenyl- (9CI)
- Magnesium, bromo-1-propenyl-
- 1-Propenylmagnesium bromide, 0.5M (7.65% w/w) in THF
- 14092-04-7
- AKOS024262735
- prop-1-enylmagnesium bromide
- (z)-prop-1-enylmagnesium bromide
- DTXSID901309034
- 1-Propenylmagnesium bromide
-
- MDL: MFCD00209610
- Inchi: 1S/C3H5.BrH.Mg/c1-3-2;;/h1,3H,2H3;1H;/q-1;;+2/p-1
- InChI Key: WQMNNHNWITXOAH-UHFFFAOYSA-M
- SMILES: [Br-].[Mg+2].C(=[CH-])C
Computed Properties
- Exact Mass: 143.94300
- Monoisotopic Mass: 143.94250g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 0
- Heavy Atom Count: 5
- Rotatable Bond Count: 0
- Complexity: 14.4
- Covalently-Bonded Unit Count: 3
- 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: nothing
- Topological Polar Surface Area: 0?2
Experimental Properties
- Color/Form: Not available
- Density: 0.95?g/mL?at 25?°C
- Boiling Point: 65?°C
- Flash Point: Fahrenheit: -4 ° f
Celsius: -20 ° c - PSA: 0.00000
- LogP: 1.91490
- Color/Form: 0.5?M in THF
- Solubility: Not available
1-Propenylmagnesium bromide Security Information
-
Symbol:
- Signal Word:Danger
- Hazard Statement: H225-H260-H302-H314-H335-H351
- Warning Statement: P210-P231+P232-P280-P370+P378-P402+P404-P403+P235
- Hazardous Material transportation number:UN 3399 4.3/PG 1
- WGK Germany:3
- Hazard Category Code: 11-15-19-36/37/38-40
- Safety Instruction: S16; S26; S27; S36/37/39; S45
-
Hazardous Material Identification:
- Risk Phrases:R11; R14/15; R19; R20/21/22; R34
- Storage Condition:2-8°C
1-Propenylmagnesium bromide Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | SA03384-2L |
1-Propenylmagnesium Bromide |
14092-04-7 | 2L |
¥12928.0 | 2021-09-03 | ||
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | SA03384-800ml |
1-Propenylmagnesium Bromide |
14092-04-7 | - | 800ml |
¥4508.0 | 2024-07-18 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | SA03384-100ml |
1-Propenylmagnesium Bromide |
14092-04-7 | 100ml |
¥1338.0 | 2021-09-03 | ||
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | A-WG133-25ml |
1-Propenylmagnesium bromide |
14092-04-7 | 0.5mol/L in THF,9dingseal | 25ml |
464.0CNY | 2021-07-16 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | A-WG133-100ml |
1-Propenylmagnesium bromide |
14092-04-7 | 0.5mol/L in THF,9dingseal | 100ml |
1205.0CNY | 2021-07-16 | |
| XI GE MA AO DE LI QI ( SHANG HAI ) MAO YI Co., Ltd. | 419540-100ML |
1-Propenylmagnesium bromide |
14092-04-7 | 0.5M in THF | 100ML |
¥1080.19 | 2022-02-24 | |
| XI GE MA AO DE LI QI ( SHANG HAI ) MAO YI Co., Ltd. | 419540-800ML |
1-Propenylmagnesium bromide |
14092-04-7 | 0.5M in THF | 800ML |
¥4311.76 | 2022-02-24 | |
| TRC | P769020-50ml |
1-Propenylmagnesium bromide |
14092-04-7 | 50ml |
140.00 | 2021-07-19 | ||
| TRC | P769020-100ml |
1-Propenylmagnesium bromide |
14092-04-7 | 100ml |
220.00 | 2021-07-19 | ||
| TRC | P769020-500ml |
1-Propenylmagnesium bromide |
14092-04-7 | 500ml |
770.00 | 2021-07-19 |
1-Propenylmagnesium bromide Suppliers
1-Propenylmagnesium bromide Related Literature
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Christopher B. Rodell,Christopher B. Highley,Minna H. Chen,Neville N. Dusaj,Chao Wang,Lin Han,Jason A. Burdick Soft Matter, 2016,12, 7839-7847
-
2. Fe3O4/Au/Fe3O4 nanoflowers exhibiting tunable saturation magnetization and enhanced bioconjugationFeng Shi,Kunping Yan,Mingli Peng,Xiao Cheng,Yanling Luo,Xuemei Chen,V. A. L. Roy,Zuankai Wang Nanoscale, 2012,4, 747-751
-
Eunkyung Choi,Minjoo Ryu,Haeri Lee,Ok-Sang Jung Dalton Trans., 2017,46, 4595-4601
-
Fereshteh Bayat Environ. Sci.: Nano, 2021,8, 367-389
-
Tengfei Yu,Yuehan Wu,Wei Li,Bin Li RSC Adv., 2014,4, 34134-34143
Additional information on 1-Propenylmagnesium bromide
Recent Advances in the Application of 1-Propenylmagnesium Bromide (CAS 14092-04-7) in Chemical and Biomedical Research
1-Propenylmagnesium bromide (CAS 14092-04-7) is a highly reactive Grignard reagent that has garnered significant attention in recent years due to its versatile applications in organic synthesis and pharmaceutical development. This research briefing aims to summarize the latest advancements in the utilization of this compound, focusing on its role in the synthesis of complex molecules, drug discovery, and biomedical applications. The findings presented here are based on a comprehensive review of recent peer-reviewed publications, patents, and industry reports.
Recent studies have highlighted the efficacy of 1-Propenylmagnesium bromide in facilitating carbon-carbon bond formation, a critical step in the synthesis of bioactive compounds. For instance, a 2023 study published in the Journal of Organic Chemistry demonstrated its utility in the stereoselective synthesis of allylic alcohols, which are key intermediates in the production of antiviral and anticancer agents. The study reported a yield improvement of up to 15% compared to traditional methods, underscoring the reagent's potential for large-scale pharmaceutical manufacturing.
In the realm of drug discovery, 1-Propenylmagnesium bromide has been employed in the development of novel kinase inhibitors. A collaborative research effort between academia and industry, documented in a 2024 Nature Communications article, utilized this reagent to synthesize a library of small molecules targeting aberrant kinase activity in cancer cells. The resulting compounds exhibited promising in vitro and in vivo efficacy, with one candidate advancing to preclinical trials. This highlights the reagent's role in accelerating the discovery of next-generation therapeutics.
Beyond synthetic chemistry, 1-Propenylmagnesium bromide has also found applications in biomedical research. A groundbreaking study published in ACS Chemical Biology in 2023 explored its use in the modification of biomolecules, such as peptides and nucleic acids, for targeted drug delivery. The researchers successfully conjugated the reagent to a tumor-homing peptide, enhancing its cellular uptake and therapeutic payload delivery. This innovative approach opens new avenues for precision medicine and personalized therapies.
Despite its advantages, challenges remain in the handling and storage of 1-Propenylmagnesium bromide due to its high reactivity and sensitivity to moisture. Recent advancements in stabilizing formulations, as detailed in a 2024 patent application, have addressed some of these issues by introducing novel protective coatings and solvent systems. These developments are expected to broaden the reagent's applicability in industrial and laboratory settings.
In conclusion, 1-Propenylmagnesium bromide (CAS 14092-04-7) continues to be a valuable tool in chemical and biomedical research, with recent studies showcasing its potential in drug synthesis, discovery, and delivery. Ongoing innovations in its formulation and application are likely to further enhance its utility, making it a cornerstone reagent in the field. Future research should focus on optimizing its use in green chemistry and sustainable pharmaceutical production to align with global environmental goals.
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