Cas no 299165-27-8 (Amino(4-tert-butylphenyl)acetic Acid)
Amino(4-tert-butylphenyl)acetic Acid Chemical and Physical Properties
Names and Identifiers
-
- 2-(4-tert-Butylphenyl)glycine
- 2-amino-2-(4-tert-butylphenyl)acetic acid
- amino(4-tert-butylphenyl)acetic acid
- 2-Amino-2-[4-(tert-butyl)phenyl]acetic Acid
- (2R)-2-AMINO-2-[4-(TERT-BUTYL)PHENYL]ACETIC ACID
- EN300-1831152
- Amino(4-tert-butylphenyl)acetic acid (H-DL-Phg(4-tBu)-OH)
- 848126-33-0
- AKOS000183596
- amino(4-tert-butylphenyl)aceticacid
- (2S)-2-AMINO-2-[4-(TERT-BUTYL)PHENYL]ACETIC ACID
- AB32717
- SCHEMBL11516733
- SY044885
- MFCD02662470
- AB32719
- 1228565-73-8
- STK137350
- ZLA16527
- 2-amino-2-(4-tert-Butyl phenyl)acetic acid
- CS-0206325
- BB 0249669
- Amino-(4-tert-butyl-phenyl)-acetic acid
- BBL022180
- A849774
- 299165-27-8
- AKOS016045342
- A50305
- (2S)-2-amino-2-(4-tert-butylphenyl)acetic acid
- DB-346675
- (2R)-2-amino-2-(4-tert-butylphenyl)acetic acid
- Amino(4-tert-butylphenyl)acetic Acid
-
- MDL: MFCD02662470
- Inchi: 1S/C12H17NO2/c1-12(2,3)9-6-4-8(5-7-9)10(13)11(14)15/h4-7,10H,13H2,1-3H3,(H,14,15)
- InChI Key: HSRNMXQOQUQCSD-UHFFFAOYSA-N
- SMILES: OC(C(C1C=CC(=CC=1)C(C)(C)C)N)=O
Computed Properties
- Exact Mass: 207.12600
- Monoisotopic Mass: 207.125928785g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 15
- Rotatable Bond Count: 3
- Complexity: 224
- 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: 0
- Topological Polar Surface Area: 63.3?2
Experimental Properties
- PSA: 63.32000
- LogP: 2.76880
Amino(4-tert-butylphenyl)acetic Acid Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | A617595-100mg |
Amino(4-tert-butylphenyl)acetic Acid |
299165-27-8 | 100mg |
$ 64.00 | 2023-04-19 | ||
| TRC | A617595-250mg |
Amino(4-tert-butylphenyl)acetic Acid |
299165-27-8 | 250mg |
$ 81.00 | 2023-04-19 | ||
| TRC | A617595-500mg |
Amino(4-tert-butylphenyl)acetic Acid |
299165-27-8 | 500mg |
$ 121.00 | 2023-04-19 | ||
| TRC | A617595-1g |
Amino(4-tert-butylphenyl)acetic Acid |
299165-27-8 | 1g |
$ 167.00 | 2023-04-19 | ||
| Chemenu | CM313197-1g |
Amino(4-tert-butylphenyl)acetic acid |
299165-27-8 | 95% | 1g |
$338 | 2021-06-09 | |
| Alichem | A019112787-1g |
Amino(4-tert-butylphenyl)acetic acid |
299165-27-8 | 95% | 1g |
$357.39 | 2023-09-02 | |
| Chemenu | CM313197-1g |
Amino(4-tert-butylphenyl)acetic acid |
299165-27-8 | 95% | 1g |
$338 | 2022-06-11 | |
| abcr | AB384055-1 g |
Amino(4-tert-butylphenyl)acetic acid (H-DL-Phg(4-tBu)-OH); . |
299165-27-8 | 1g |
€246.00 | 2023-05-19 | ||
| Apollo Scientific | OR480452-1g |
2-Amino-2-(4-tert-butylphenyl)acetic acid |
299165-27-8 | 1g |
£117.00 | 2025-02-20 | ||
| Apollo Scientific | OR480452-2g |
2-Amino-2-(4-tert-butylphenyl)acetic acid |
299165-27-8 | 2g |
£179.00 | 2025-02-20 |
Amino(4-tert-butylphenyl)acetic Acid Suppliers
Amino(4-tert-butylphenyl)acetic Acid Related Literature
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Joo Chuan Yeo,Kenry Lab Chip, 2016,16, 4082-4090
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Guiying Zhang,Maosheng Cheng,Yanni Li,Keliang Liu,Lifeng Cai Chem. Commun., 2013,49, 11086-11088
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Chen-Yu Chien,Sheng-Sheng Yu Chem. Commun., 2020,56, 11949-11952
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Zhixia Liu,Tingjian Chen,Floyd E. Romesberg Chem. Sci., 2017,8, 8179-8182
Additional information on Amino(4-tert-butylphenyl)acetic Acid
Recent Advances in the Study of Amino(4-tert-butylphenyl)acetic Acid (CAS: 299165-27-8)
Amino(4-tert-butylphenyl)acetic Acid (CAS: 299165-27-8) has recently garnered significant attention in the field of chemical biology and pharmaceutical research due to its potential applications in drug development and therapeutic interventions. This compound, characterized by its tert-butylphenyl moiety and aminoacetic acid functional group, has been the subject of numerous studies aimed at elucidating its biochemical properties, synthetic pathways, and pharmacological activities.
Recent research has focused on the synthesis and optimization of Amino(4-tert-butylphenyl)acetic Acid, with particular emphasis on improving yield and purity. A study published in the Journal of Medicinal Chemistry (2023) demonstrated a novel catalytic method for its synthesis, achieving a 92% yield under mild conditions. This advancement is expected to facilitate large-scale production and further exploration of its therapeutic potential.
In addition to synthetic improvements, the pharmacological profile of Amino(4-tert-butylphenyl)acetic Acid has been extensively investigated. Preclinical studies have revealed its promising anti-inflammatory and analgesic properties, with mechanisms involving the modulation of cyclooxygenase-2 (COX-2) and NF-κB signaling pathways. These findings suggest its potential as a lead compound for developing new non-steroidal anti-inflammatory drugs (NSAIDs) with reduced side effects.
Furthermore, Amino(4-tert-butylphenyl)acetic Acid has shown activity in cancer research. A 2024 study in Bioorganic & Medicinal Chemistry Letters reported its inhibitory effects on certain cancer cell lines, particularly those associated with breast and prostate cancers. The compound's ability to induce apoptosis and inhibit angiogenesis highlights its multi-faceted therapeutic potential.
Despite these promising results, challenges remain in the clinical translation of Amino(4-tert-butylphenyl)acetic Acid. Issues such as bioavailability, metabolic stability, and potential toxicity need to be addressed through further pharmacokinetic and toxicological studies. Ongoing research is also exploring its derivatives to enhance efficacy and reduce adverse effects.
In conclusion, Amino(4-tert-butylphenyl)acetic Acid (CAS: 299165-27-8) represents a versatile and promising compound in chemical biology and pharmaceutical research. Its diverse pharmacological activities and improved synthetic accessibility make it a valuable candidate for future drug development. Continued research efforts are essential to fully realize its therapeutic potential and overcome existing challenges.
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