Cas no 67346-49-0 (Arformoterol)
Arformoterol Chemical and Physical Properties
Names and Identifiers
-
- Arformoterol base
- (R,R)-Formoterol
- Arformoterol
- Formamide, N-[2-hydroxy-5-[(1R)-1-hydroxy-2-[[(1R)-2-(4-methoxyphenyl)-1-methylethyl]amino]ethyl]phenyl]-, (2R,3R)-
- (-)-Formoterol
- N-[2-Hydroxy-5-[1(R)-hydroxy-2-[2-(4-methoxyphenyl)-1(R)-methylethylamino]ethyl]phenyl]formamide
- FORMOTEROL [INN]
- ARFORMOTEROL [VANDF]
- (-)-N-(2-HYDROXY-5-((1R)-1-HYDROXY-2-(((1R)-2-(4-METHOXYPHENYL)-1-METHYLETHYL)AMINO)ETHYL)PHENYL)FORMAMIDE HYDROGEN (2R,3R)-2,3-DIHYDROXYBUTANEDIOATE
- Fluir
- FORMOTEROL [MI]
- (+-)-2'-Hydroxy-5'-((RS)-1-hydroxy-2-(((RS)-p-methoxy-alpha-methylphenethyl)amino)ethyl)formanilide
- N-[2-hydroxy-5-[(1R)-1-hydroxy-2-[[(2R)-1-(4-methoxyphenyl)propan-2-yl]amino]ethyl]phenyl]formamide
- CHEBI:408174
- N-(2-hydroxy-5-((R)-1-hydroxy-2-((R)-1-(4-methoxyphenyl)propan-2-ylamino)ethyl)phenyl)formamide
- N-(2-Hydroxy-5-{1-hydroxy-2-[2-(4-methoxy-phenyl)-1-methyl-ethylamino]-ethyl}-phenyl)-formamide
- Oxis
- formoterol
- (+-)-Formoterol
- n-[2-hydroxy-5-[(1r)-1-hydroxy-2-[[(1r)-2-(4-methoxyphenyl)-1-methylethyl]amino]ethyl]phenyl]formamide
- eformoterol
- UNII-5ZZ84GCW8B
- HSDB 7287
- Arformoterol (INN)
- Q4789167
- D87655
- EN300-174504
- Formamide, N-(2-hydroxy-5-((1R)-1-hydroxy-2-(((1R)-2-(4-methoxyphenyl)-1-methylethyl)amino)ethyl)phenyl)-
- FORMOTEROL R,R-FORM [MI]
- D07463
- Atimos
- N-(2-hydroxy-5-((1R)-1-hydroxy-2-(((2R)-1-(4-methoxyphenyl)propan-2-yl)amino)ethyl)phenyl)formamide
- AKOS015969668
- 5ZZ84GCW8B
- Formamide, N-[2-hydroxy-5-[(1R)-1-hydroxy-2-[[(1R)-2-(4-methoxyphenyl)-1-methylethyl]amino]ethyl]phenyl]-
- Racemic formoterol
- MFCD05662345
- DTXSID40110071
- Formoterol [USAN:INN:BAN]
- F91H02EBWT
- SCHEMBL4247
- Foradil
- UNII-F91H02EBWT
- YM-08316
- Perforomist
- Formamide, N-(2-hydroxy-5-(1-hydroxy-2-((2-(4-methoxyphenyl)-1-methylethyl)amino)ethyl)phenyl)-, (R-(R*,R*))-
- arformoterolum
- ARFORMOTEROL [WHO-DD]
- rel-n-[2-hydroxy-5-[(1r)-1-hydroxy-2-[[(1r)-2-(4-methoxyphenyl)-1-methylethyl]amino]ethyl]phenyl]formamide
- BDBM50151720
- Innovair
- FORMOTEROL [WHO-DD]
- Arformoterol [INN]
- NS00120489
- 73573-87-2
- 67346-49-0
- FORMOTEROL FUMARATE
- DB01274
- Formoterol r,r-form
- FORMOTEROL [HSDB]
- GTPL7479
- FORMAMIDE, N-(2-HYDROXY-5-(1-HYDROXY-2-((2-(4-METHOXYPHENYL)-1-METHYLETHYL)AMINO)ETHYL)PHENYL)-
- formoterol, ((R*,R*)-(+-))-isomer
- CHEMBL1363
- BPZSYCZIITTYBL-YJYMSZOUSA-N
- cid_9912089
- Formoterolum
- FORMOTEROL [VANDF]
- N-{2-hydroxy-5-[(1R)-1-hydroxy-2-({(1R)-1-methyl-2-[4-(methyloxy)phenyl]ethyl}amino)ethyl]phenyl}formamide
- N-{2-hydroxy-5-[(1R)-1-hydroxy-2-{[(2R)-1-(4-methoxyphenyl)propan-2-yl]amino}ethyl]phenyl}formamide
- H98
- HY-B0010A
- CS-1413
-
- MDL: MFCD00864141
- Inchi: 1S/C19H24N2O4/c1-13(9-14-3-6-16(25-2)7-4-14)20-11-19(24)15-5-8-18(23)17(10-15)21-12-22/h3-8,10,12-13,19-20,23-24H,9,11H2,1-2H3,(H,21,22)/t13-,19+/m1/s1
- InChI Key: BPZSYCZIITTYBL-YJYMSZOUSA-N
- SMILES: [C@H](C1C=CC(O)=C(NC=O)C=1)(O)CN[C@H](C)CC1C=CC(OC)=CC=1
Computed Properties
- Exact Mass: 344.17400
- Monoisotopic Mass: 344.174
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 4
- Hydrogen Bond Acceptor Count: 6
- Heavy Atom Count: 25
- Rotatable Bond Count: 9
- Complexity: 388
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 2
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 90.8A^2
- XLogP3: 1.8
Experimental Properties
- Color/Form: Gray white solid
- Density: 1.233
- Boiling Point: 603.2°C at 760 mmHg
- Flash Point: 318.6 oC
- Refractive Index: 1.616
- PSA: 90.82000
- LogP: 3.32310
Arformoterol Security Information
- Signal Word:Warning
- Hazard Statement: H302-H315-H319-H335
- Warning Statement: P261-P305+P351+P338
Arformoterol Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | R864579-10mg |
(R,R)-Formoterol |
67346-49-0 | ≥98.0% | 10mg |
¥565.20 | 2022-09-28 | |
| TRC | F693443-1mg |
(R,R)-Formoterol (Arformoterol) |
67346-49-0 | 1mg |
$190.00 | 2023-05-18 | ||
| TRC | F693443-10mg |
(R,R)-Formoterol (Arformoterol) |
67346-49-0 | 10mg |
$1499.00 | 2023-05-18 | ||
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | R46300-10mg |
Formoterol |
67346-49-0 | 10mg |
¥678.0 | 2021-09-08 | ||
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | R46300-50mg |
Formoterol |
67346-49-0 | 50mg |
¥2818.0 | 2021-09-08 | ||
| SHANG HAI YI EN HUA XUE JI SHU Co., Ltd. | R025317-10mg |
(R,R)-Formoterol,98% |
67346-49-0 | 98% | 10mg |
¥732 | 2024-05-22 | |
| SHANG HAI YI EN HUA XUE JI SHU Co., Ltd. | R025317-50mg |
(R,R)-Formoterol,98% |
67346-49-0 | 98% | 50mg |
¥3337 | 2024-05-22 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | L-VS726-10mg |
(R,R)-Formoterol |
67346-49-0 | ≥98.0% | 10mg |
¥924.0 | 2022-02-28 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | L-VS726-2mg |
(R,R)-Formoterol |
67346-49-0 | ≥98.0% | 2mg |
¥275.0 | 2022-02-28 | |
| MedChemExpress | HY-B0010A-5mg |
Arformoterol |
67346-49-0 | ≥98.0% | 5mg |
¥2900 | 2024-04-19 |
Arformoterol Suppliers
Arformoterol Related Literature
-
Patricia A. A. M. Vaz,Jo?o Rocha,Artur M. S. Silva New J. Chem., 2016,40, 8198-8201
-
Adeline Huiling Loo,Alessandra Bonanni,Martin Pumera Analyst, 2013,138, 467-471
-
Zhonghua Xiang,Chuanqi Fang,Sanhua Leng,Dapeng Cao J. Mater. Chem. A, 2014,2, 7662-7665
-
Christian K. Rank,Alexander W. Jones,Tatjana Wall,Patrick Di Martino-Fumo,Sarah Schr?ck,Markus Gerhards,Frederic W. Patureau Chem. Commun., 2019,55, 13749-13752
-
5. An all-solid-state imprinted polymer-based potentiometric sensor for determination of bisphenol S?Rongning Liang,Tanji Yin,Ruiqing Yao,Wei Qin RSC Adv., 2016,6, 73308-73312
Additional information on Arformoterol
Comprehensive Overview of Arformoterol (CAS No. 67346-49-0): Mechanism, Applications, and Emerging Trends
Arformoterol (CAS No. 67346-49-0), a selective β2-adrenergic receptor agonist, is a long-acting bronchodilator primarily used in the management of chronic obstructive pulmonary disease (COPD) and asthma. Its chemical structure, (R,R)-formoterol, distinguishes it as the active enantiomer of racemic formoterol, offering enhanced efficacy and reduced side effects. The compound’s unique pharmacological profile has made it a subject of interest in respiratory therapeutics, particularly amid rising global concerns over air pollution and respiratory health.
In recent years, the demand for Arformoterol-based treatments has surged, driven by increasing COPD prevalence and patient awareness. Search trends reveal frequent queries such as "Arformoterol vs. salmeterol" and "best bronchodilator for severe asthma," reflecting its clinical relevance. The drug’s ultra-LABA (ultra-long-acting beta-agonist) properties ensure sustained bronchodilation for up to 24 hours, addressing unmet needs in respiratory disease management.
From a molecular perspective, Arformoterol (CAS No. 67346-49-0) binds selectively to β2-receptors in bronchial smooth muscle, activating adenylate cyclase and increasing cyclic AMP. This mechanism relaxes airways, improving airflow and reducing symptoms like wheezing. Notably, its enantiomeric purity minimizes off-target effects on cardiac β1-receptors, a key advantage over older bronchodilators.
Current research explores Arformoterol’s synergy with inhaled corticosteroids (ICS) and anticholinergics, aligning with the GOLD guidelines for COPD combo therapy. Studies also investigate its potential in exercise-induced bronchoconstriction, a hot topic among athletes and fitness enthusiasts. As precision medicine gains traction, Arformoterol’s role in personalized respiratory care is increasingly emphasized.
Manufacturing and formulation advancements have optimized Arformoterol’s delivery via nebulizers and dry powder inhalers (DPIs). Patients frequently search for "how to use Arformoterol nebulizer" or "Arformoterol side effects," underscoring the need for clear patient education. The drug’s stability profile and low systemic absorption further enhance its safety.
In conclusion, Arformoterol (CAS No. 67346-49-0) represents a cornerstone in modern respiratory pharmacotherapy. Its targeted action, coupled with evolving applications, positions it as a vital tool against global respiratory disease burdens. Future directions may include digital health integrations, such as smart inhalers, to optimize adherence and outcomes.
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