
CAS Number71989-14-5
SynonymsL-Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 4-(1,1-dimethylethyl) ester; FMOC-L-Asparticacidbeta-tert-butylester; 4-tert-Butyl hydrogen N-((9H-fluoren-9-ylmethoxy)carbonyl)-L-aspartate; (2S)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-4-[(2-methyl-2-propanyl)oxy]-4-oxobutanoic acid; MFCD00037131; FMOC-L-Aspartic acid beta-tert-butyl ester; N-α-FMOC-L-aspartic acid β-tert-butyl ester; Fmoc-L-aspartic acid 4-tert-butyl ester; Fmoc-Asp(OtBu)-OH; EINECS 276-251-7; 9-fluorenyl-methoxycarbonyl-L-Asp-tert-butyl ester
Molecular FormulaC23H25NO6
Molecular Weight411.45
Purity≥98.0 (HPLC)%
Density1.3±0.1 g/cm3
Boiling Point620.8±55.0 °C at 760 mmHg
Melting Point148-150 °C (dec.)
Appearancepowder
EINECS276-251-7
Symbol
Signal WordWarning
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| Chemical & Physical Properties | |
|---|---|
| CAS Number | 71989-14-5 |
| Catalog No. | 2A-9007827 |
| Chinese Name | Fmoc-L-天冬氨酸-4-叔丁酯 |
| Synonyms | L-Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 4-(1,1-dimethylethyl) ester; FMOC-L-Asparticacidbeta-tert-butylester; 4-tert-Butyl hydrogen N-((9H-fluoren-9-ylmethoxy)carbonyl)-L-aspartate; (2S)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-4-[(2-methyl-2-propanyl)oxy]-4-oxobutanoic acid; MFCD00037131; FMOC-L-Aspartic acid beta-tert-butyl ester; N-α-FMOC-L-aspartic acid β-tert-butyl ester; Fmoc-L-aspartic acid 4-tert-butyl ester; Fmoc-Asp(OtBu)-OH; EINECS 276-251-7; 9-fluorenyl-methoxycarbonyl-L-Asp-tert-butyl ester |
| Molecular Formula | C23H25NO6 |
| Molecular Weight | 411.45 |
| Purity | ≥98.0 (HPLC) |
| Density | 1.3±0.1 g/cm3 |
| Boiling Point | 620.8±55.0 °C at 760 mmHg |
| Melting Point | 148-150 °C (dec.) |
| Appearance | powder |
| Storage Condition | Store in an airtight container in a cool, dry plac |
| Application | Fmoc Asp(OtBu)-OH (4-tert-butyl N-(fluoren-9-ylmethoxycarbonyl)-L-aspartic acid) is an aspartic acid ester derivative containing the amine protecting group Fmoc. Fmoc-Asp(OtBu)-OH can be used for pept |
| EINECS | 276-251-7 |
| HTC | 2924299090 |
| PubChem ID | 57651040 |
| MDL Number | MFCD00037131 |
| SMILES | CC(C)(C)OC(=O)C[C@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O |
| InChI | 1S/C23H25NO6/c1-23(2,3)30-20(25)12-19(21(26)27)24-22(28)29-13-18-16-10-6-4-8-14(16)15-9-5-7-11-17(15)18/h4-11,18-19H,12-13H2,1-3H3,(H,24,28)(H,26,27)/t19-/m0/s1 |
| InChI Key | FODJWPHPWBKDON-IBGZPJMESA-N |
| Beilstein/REAXYS | 3635671 |
| NACRES Code | NA.26 |
| eCl@ss | 32160406 |
| UNSPSC | 12352209 |
| Hazard Symbols | Transport |
| MSDS | msds/7827_1_71989_14_5.pdf |
| Bioactivity | Fmoc-Asp(OtBu)-OH (4-tert-Butyl N-(fluoren-9-ylmethoxycarbonyl)-L-aspartate) is a aspartate derivative containing amine protecting group Fmoc. Fmoc-Asp(OtBu)-OH can be used for peptide synthesis[1]. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others References [1]. Esquivel J B, et al. Chiral HPLC separation of protected amino acids. Journal of liquid chromatography & related technologies, 1998, 21(6): 777-791. Chemical & Physical Properties Density 1.3±0.1 g/cm3 Boiling Point 620.8±55.0 °C at 760 mmHg Melting Point 148-150 °C (dec.) Molecular Formula C23H25NO6 Molecular Weight 411.448 Flash Point 329.3±31.5 °C Exact Mass 411.168182 PSA 101.93000 LogP 5.16 Vapour Pressure 0.0±1.9 mmHg at 25°C Index of Refraction 1.576 InChIKey FODJWPHPWBKDON-IBGZPJMESA-N SMILES CC(C)(C)OC(=O)CC(NC(=O)OCC1c2ccccc2-c2ccccc21)C(=O)O Storage condition 2~8°C |
| Use of | Fmoc-Asp(OtBu)-OH (4-tert-Butyl N-(fluoren-9-ylmethoxycarbonyl)-L-aspartate) is a aspartate derivative containing amine protecting group Fmoc. Fmoc-Asp(OtBu)-OH can be used for peptide synthesis[1]. Properties Name FMOC-L-Aspartic acid β-tert-butyl ester Synonym More Synonyms FMOC-ASP(OTBU)-OH Biological Activity Description Fmoc-Asp(OtBu)-OH (4-tert-Butyl N-(fluoren-9-ylmethoxycarbonyl)-L-aspartate) is a aspartate derivative containing amine protecting group Fmoc. Fmoc-Asp(OtBu)-OH can be used for peptide synthesis[1]. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others References [1]. Esquivel J B, et al. Chiral HPLC separation of protected amino acids. Journal of liquid chromatography & related technologies, 1998, 21(6): 777-791. Chemical & Physical Properties Molecular Formula C23H25NO6 Exact Mass 411.168182 PSA 101.93000 Index of Refraction 1.576 InChIKey FODJWPHPWBKDON-IBGZPJMESA-N |
| Tax Rebate | 13.0% |
| Supervision | None. MFN tariff: 6.5%. Ordinary tariff: 30.0% |
| Transport Info | Shipping Name: UN |
| MSDS Transport Info | Module 14. Shipping information 14.1 UN dangerous goods number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 United Nations shipping name European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Danger Regulations: No International Maritime Danger Regulations International Air Transport Danger Regulations: No Marine pollutants (yes/no): No 14.6 Special reminder to users No data available |
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| Fmoc-Asn-OH | 71989-16-7 | 2A-9007824 |
| Fmoc-Asp(OBzl)-OH | 86060-84-6 | 2A-9007825 |
| Fmoc-Asp(OcHex)-OH | 130304-80-2 | 2A-9007826 |
| Fmoc-Asp(OtBu)-Opfp | 86061-01-0 | 2A-9007828 |
| Fmoc-Asp-OBzl | 86060-83-5 | 2A-9007829 |
| Fmoc-beta-Ala-OH | 35737-10-1 | 2A-9007830 |
| Fmoc-Cl; 9-Fluorenylmethyl chloroformate | 28920-43-6 | 2A-9007831 |
| Fmoc-Cys(Acm)-OH | 86060-81-3 | 2A-9007832 |
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