CAS Number20866-48-2
SynonymsN,O-Bis{[(2-methyl-2-propanyl)oxy]carbonyl}-L-tyrosine; N,O-Bis[(1,1-dimethylethoxy)carbonyl]-L-tyrosine; BOC-TYR(BOC)-OH; N,O-di-tert-butyloxycarbonyl-L-tyrosine; Boc-L-Tyr(Boc)-OH; N-Boc-L-Tyr(OBoc)-OH; AmbotzBAA1444; Boc-L-Tyr(OBoc)-OH; N,O-bis-Boc-L-tyrosine; N,O-bis(tert-butoxycarbonyl)-L-tyrosine; N,O-(di-t-butoxycarbonyl)-L-tyrosine; N,O-di-BOC-L-tyrosine
Molecular FormulaC19H27NO7
Molecular Weight381.43
Purity96+%
Density1.2±0.1 g/cm3
Boiling Point528.4±50.0 °C at 760 mmHg
EINECS0
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 20866-48-2 |
| Catalog No. | 2A-0151751 |
| Chinese Name | N,O-双[(叔丁氧基)羰基]-L-酪氨酸 |
| Synonyms | N,O-Bis{[(2-methyl-2-propanyl)oxy]carbonyl}-L-tyrosine; N,O-Bis[(1,1-dimethylethoxy)carbonyl]-L-tyrosine; BOC-TYR(BOC)-OH; N,O-di-tert-butyloxycarbonyl-L-tyrosine; Boc-L-Tyr(Boc)-OH; N-Boc-L-Tyr(OBoc)-OH; AmbotzBAA1444; Boc-L-Tyr(OBoc)-OH; N,O-bis-Boc-L-tyrosine; N,O-bis(tert-butoxycarbonyl)-L-tyrosine; N,O-(di-t-butoxycarbonyl)-L-tyrosine; N,O-di-BOC-L-tyrosine |
| Molecular Formula | C19H27NO7 |
| Molecular Weight | 381.43 |
| Purity | 96+ |
| Density | 1.2±0.1 g/cm3 |
| Boiling Point | 528.4±50.0 °C at 760 mmHg |
| Storage Condition | 2-8°C |
| Application | Boc-Tyr(Boc)-OH is an amino acid derivative that can be used in compound synthesis [1]. |
| EINECS | 0 |
| HTC | 2924299090 |
| UN(IATA) | 0 |
| PubChem ID | 43608015 |
| SMILES | CC(C)(C)OC(=O)NC(Cc1ccc(OC(=O)OC(C)(C)C)cc1)C(=O)O |
| InChI | InChI=1S/C19H27NO7/c1-18(2,3)26-16(23)20-14(15(21)22)11-12-7-9-13(10-8-12)25-17(24)27-19(4,5)6/h7-10,14H,11H2,1-6H3,(H,20,23)(H,21,22)/t14-/m0/s1 |
| InChI Key | MRYIHKCPPKHOPJ-AWEZNQCLSA-N |
| Use of | Boc-Tyr(Boc)-OH is an amino acid derivative that can be used for compound synthesis[1]. Properties Name (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-[4-[(2-methylpropan-2-yl)oxycarbonyloxy]phenyl]propanoic acid Synonym More Synonyms Boc-tyr(boc)-oh Biological Activity Description Boc-Tyr(Boc)-OH is an amino acid derivative that can be used for compound synthesis[1]. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others References [1]. Osaka K, et al. Sequential Intermolecular Radical Addition and Reductive Radical Cyclization of Tyrosine and Phenylalanine Derivatives with Alkenes via Photoinduced Decarboxylation: Access to Ring-Constrained γ-Amino Acids. J Org Chem. 2019 Aug 2;84(15):9480-9488. Chemical & Physical Properties Molecular Formula C19H27NO7 Exact Mass 381.178741 PSA 111.16000 Index of Refraction 1.517 InChIKey MRYIHKCPPKHOPJ-AWEZNQCLSA-N Safety Information Hazard Codes Xi HS Code 2924299090 Synthetic Route Total: 1 Page Di-tert-butyl d... CAS#:24424-99-5 Boc-Tyr-OH CAS#:3978-80-1 Boc-tyr(boc)-oh CAS#:20866-48-2 Literature: Nakamura, Kozo; Nakajima, Takero; Kayahara, Hiroshi; Nomura, Eisaku; Taniguchi, Hisaji Tetrahedron Letters, 2004 , vol. 45, # 3 p. 495 - 499 Di-tert-butyl d... CAS#:24424-99-5 L-Tyrosine CAS#:60-18-4 Boc-tyr(boc)-oh CAS#:20866-48-2 Literature: Pozdnev, V. F. Chemistry of Natural Compounds, 1982 , vol. 18, # 1 p. 125 - 126 Khimiya Prirodnykh Soedinenii, 1982 , vol. 18, # 1 p. 129 - 130 tert-butyl fluo... CAS#:18595-34-1 L-Tyrosine CAS#:60-18-4 Boc-tyr(boc)-oh CAS#:20866-48-2 Literature: Justus Liebigs Annalen der Chemie, , vol. 716, p. 175 - 185 Precursor & DownStream Precursor 3 CAS#:24424-99-5 Di-tert-butyl d... CAS#:3978-80-1 Boc-Tyr-OH CAS#:60-18-4 L-Tyrosine DownStream 5 CAS#:88829-53-2 Glycine, N-[N-[... CAS#:2387-23-7 1,3-Dicyclohexylurea CAS#:119975-64-3 Deltorphin CAS#:122752-15-2 Deltorphin I TFA |
| Tax Rebate | 13.0% |
| Supervision | None. MFN tariff: 6.5%. Ordinary tariff: 30.0% |
| Transport Info | Product name: Summary 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
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