Cas no 29122-74-5 (4-2-Hydroxy-3-(1-methylethyl)aminopropoxybenzaldehyde)
4-2-Hydroxy-3-(1-methylethyl)aminopropoxybenzaldehyde Chemical and Physical Properties
Names and Identifiers
-
- 4-[2-Hydroxy-3-[(1-methylethyl)amino]propoxy]benzaldehyde
- 4-[2-hydroxy-3-(propan-2-ylamino)propoxy]benzaldehyde
- Benzaldehyde,4-[2-hydroxy-3-[(1-methylethyl)amino]propoxy]-
- METOPROLOL IMPURITY C
- (+/-)4-[2-Hydroxy-3-(1-Methylethyl)aMinopropoxy]benzaldehyde
- 1-p-formylphenoxy-3-isopropylamino-2-propanol
- Metoprolol related compound C
- UNII-E1ILP72SEM
- 4-2-Hydroxy-3-(1-methylethyl)aminopropoxybenzaldehyde
- Metoprolol EP impurity C/Bisoprolol EP impurity L
- EN300-649742
- Benzaldehyde, 4-[2-hydroxy-3-[(1-methylethyl)amino]propoxy]-
- J-017399
- Q27276749
- Metoprolol succinate specified impurity C [EP]
- 4-(2-Hydroxy-3-(isopropylamino)propoxy)benzaldehyde
- 4-{2-hydroxy-3-[(propan-2-yl)amino]propoxy}benzaldehyde
- (+/-)-4-(2-Hydroxy-3-(1-methylethyl)aminopropoxy)benzaldehyde
- NS00133526
- 29122-74-5
- E1ILP72SEM
- AKOS030254534
- Benzaldehyde, 4-(2-hydroxy-3-((1-methylethyl)amino)propoxy)-
- FT-0669787
- Bisoprolol EP Impurity L
- Metoprolol tartrate specified impurity C [EP]
- H-128/80
- METOPROLOL SUCCINATE IMPURITY C [EP IMPURITY]
- MFCD16251410
- 4-[[(2rs)-2-hydroxy-3-(isopropylamino)propyl]oxy]-benzaldehyde
- A929301
- SCHEMBL5317103
- Z2937742758
- C90292
- H 128/80
- Metoprolol EP Impurity C
- METOPROLOL TARTRATE IMPURITY C [EP IMPURITY]
- DB-228995
- 4-[2-HYDROXY-3-(ISOPROPYLAMINO)PROPOXY]BENZALDEHYDE
- STL450904
- BGHLBXLHZRCXRY-UHFFFAOYSA-N
-
- Inchi: 1S/C13H19NO3/c1-10(2)14-7-12(16)9-17-13-5-3-11(8-15)4-6-13/h3-6,8,10,12,14,16H,7,9H2,1-2H3
- InChI Key: BGHLBXLHZRCXRY-UHFFFAOYSA-N
- SMILES: O(C1C=CC(C=O)=CC=1)CC(CNC(C)C)O
Computed Properties
- Exact Mass: 237.13600
- Monoisotopic Mass: 237.13649347g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 17
- Rotatable Bond Count: 7
- Complexity: 213
- 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
- XLogP3: 1.2
- Topological Polar Surface Area: 58.6?2
Experimental Properties
- Color/Form: No data avaiable
- Density: 1.1±0.1 g/cm3
- Boiling Point: 402.5±35.0 °C at 760 mmHg
- Flash Point: 197.2±25.9 °C
- PSA: 58.56000
- LogP: 1.62770
- Vapor Pressure: 0.0±1.0 mmHg at 25°C
4-2-Hydroxy-3-(1-methylethyl)aminopropoxybenzaldehyde Security Information
- Signal Word:warning
- Hazard Statement: H303+H313+H333
- Warning Statement: P264+P280+P305+P351+P338+P337+P313
- Safety Instruction: H303+H313+H333
- Storage Condition:storage at -4℃ (1-2weeks), longer storage period at -20℃ (1-2years)
4-2-Hydroxy-3-(1-methylethyl)aminopropoxybenzaldehyde Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | H946735-10mg |
4-[2-Hydroxy-3-[(1-methylethyl)amino]propoxy]benzaldehyde |
29122-74-5 | 10mg |
$ 224.00 | 2023-09-07 | ||
| TRC | H946735-100mg |
4-[2-Hydroxy-3-[(1-methylethyl)amino]propoxy]benzaldehyde |
29122-74-5 | 100mg |
$ 1742.00 | 2023-09-07 | ||
| SHENG KE LU SI SHENG WU JI SHU | sc-209893-5mg |
4-[2-Hydroxy-3-[(1-methylethyl)amino]propoxy]benzaldehyde, |
29122-74-5 | 5mg |
¥2407.00 | 2023-09-05 | ||
| Enamine | EN300-649742-0.05g |
4-{2-hydroxy-3-[(propan-2-yl)amino]propoxy}benzaldehyde |
29122-74-5 | 95% | 0.05g |
$118.0 | 2023-05-05 | |
| Enamine | EN300-649742-0.1g |
4-{2-hydroxy-3-[(propan-2-yl)amino]propoxy}benzaldehyde |
29122-74-5 | 95% | 0.1g |
$176.0 | 2023-05-05 | |
| Enamine | EN300-649742-0.25g |
4-{2-hydroxy-3-[(propan-2-yl)amino]propoxy}benzaldehyde |
29122-74-5 | 95% | 0.25g |
$252.0 | 2023-05-05 | |
| Enamine | EN300-649742-0.5g |
4-{2-hydroxy-3-[(propan-2-yl)amino]propoxy}benzaldehyde |
29122-74-5 | 95% | 0.5g |
$457.0 | 2023-05-05 | |
| Enamine | EN300-649742-1.0g |
4-{2-hydroxy-3-[(propan-2-yl)amino]propoxy}benzaldehyde |
29122-74-5 | 95% | 1g |
$584.0 | 2023-05-05 | |
| Enamine | EN300-649742-2.5g |
4-{2-hydroxy-3-[(propan-2-yl)amino]propoxy}benzaldehyde |
29122-74-5 | 95% | 2.5g |
$1147.0 | 2023-05-05 | |
| Enamine | EN300-649742-5.0g |
4-{2-hydroxy-3-[(propan-2-yl)amino]propoxy}benzaldehyde |
29122-74-5 | 95% | 5g |
$1695.0 | 2023-05-05 |
4-2-Hydroxy-3-(1-methylethyl)aminopropoxybenzaldehyde Suppliers
4-2-Hydroxy-3-(1-methylethyl)aminopropoxybenzaldehyde Related Literature
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Nayana Nayek,Pintu Karmakar,Mullicka Mandal,Indrajit Karmakar,Goutam Brahmachari New J. Chem. 2022 46 13483
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Nayana Nayek,Pintu Karmakar,Mullicka Mandal,Indrajit Karmakar,Goutam Brahmachari New J. Chem. 2022 46 13483
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Sarah J. Atkinson,Vicky-June Ellis,Sue E. Boyd,Christopher L. Brown New J. Chem. 2007 31 155
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Tomoyuki Kosai,Shintaro Ishida,Takeaki Iwamoto Dalton Trans. 2017 46 11271
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Jessica Palmucci,Kamran T. Mahmudov,M. Fátima C. Guedes da Silva,Fabio Marchetti,Claudio Pettinari,Dezemona Petrelli,Luca A. Vitali,Luana Quassinti,Massimo Bramucci,Giulio Lupidi,Armando J. L. Pombeiro RSC Adv. 2016 6 4237
Additional information on 4-2-Hydroxy-3-(1-methylethyl)aminopropoxybenzaldehyde
Comprehensive Overview of 4-2-Hydroxy-3-(1-methylethyl)aminopropoxybenzaldehyde (CAS No. 29122-74-5)
4-2-Hydroxy-3-(1-methylethyl)aminopropoxybenzaldehyde (CAS No. 29122-74-5) is a specialized organic compound with significant applications in pharmaceutical and chemical research. This compound, often referred to by its systematic name, belongs to the class of benzaldehyde derivatives, which are widely studied for their versatile chemical properties and potential therapeutic benefits. The presence of both hydroxy and isopropylamino functional groups in its structure makes it a valuable intermediate in synthetic chemistry.
In recent years, the demand for benzaldehyde-based compounds has surged due to their role in drug discovery and material science. Researchers are particularly interested in 4-2-Hydroxy-3-(1-methylethyl)aminopropoxybenzaldehyde for its potential as a building block in the synthesis of bioactive molecules. Its unique structure allows for modifications that can lead to the development of novel pharmaceutical agents, addressing current health challenges such as antimicrobial resistance and chronic diseases.
The compound's CAS No. 29122-74-5 is a critical identifier for researchers and manufacturers, ensuring precise communication and regulatory compliance. With the growing emphasis on green chemistry and sustainable practices, 4-2-Hydroxy-3-(1-methylethyl)aminopropoxybenzaldehyde has also been explored for its compatibility with eco-friendly synthesis methods. This aligns with the global trend toward reducing the environmental impact of chemical production.
One of the most frequently asked questions about 4-2-Hydroxy-3-(1-methylethyl)aminopropoxybenzaldehyde revolves around its solubility and stability under various conditions. Studies indicate that the compound exhibits moderate solubility in polar solvents like ethanol and water, making it suitable for a range of laboratory applications. Its stability at room temperature further enhances its practicality for long-term storage and use.
Another area of interest is the compound's potential role in catalysis and polymer chemistry. The hydroxy and amino groups in its structure can participate in hydrogen bonding and other intermolecular interactions, which are crucial for designing advanced materials. This has led to investigations into its use as a ligand or cross-linking agent in polymer networks.
From a commercial perspective, 4-2-Hydroxy-3-(1-methylethyl)aminopropoxybenzaldehyde is gaining attention as a high-value intermediate in the fine chemicals market. Its synthesis and purification processes have been optimized to meet the stringent quality standards required by pharmaceutical and agrochemical industries. This has positioned the compound as a reliable choice for manufacturers seeking high-purity raw materials.
In conclusion, 4-2-Hydroxy-3-(1-methylethyl)aminopropoxybenzaldehyde (CAS No. 29122-74-5) represents a fascinating intersection of chemistry and innovation. Its multifaceted applications, from drug development to material science, underscore its importance in modern research. As the scientific community continues to explore its potential, this compound is poised to play a pivotal role in addressing some of the most pressing challenges in science and industry.
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