73259-81-1
73259-81-1 structure
- Name: N(Alpha)-Boc-L-2,3-Diaminopropionic Acid
- Chemical Name: N(Alpha)-Boc-L-2,3-Diaminopropionic Acid
- CAS Number: 73259-81-1
- Molecular Formula: C8H16N2O4
- Molecular Weight: 204.22
- Catalog: Biochemical Amino acids and their derivatives BOC-amino acid
- Create Date: 2018-10-07 10:39:17
- Modify Date: 2026-06-30 20:11:31
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Boc-L-Dap-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
| Name | N(Alpha)-Boc-L-2,3-Diaminopropionic Acid |
|---|---|
| Synonyms |
(2S)-3-amino-2-{[(tert-butoxy)carbonyl]amino}propanoic acid
(N-BOC-BETA-AMINO)-ALA-OH T-BUTYLOXYCBONYL-L-2,3-DIAMINOPROPIONIC ACID (2S)-3-amino-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid Nα-Boc-L-β-aminoalanine N2-(tert-Butoxycbonyl)-(S)-2,3-diaminopropionic acid Boc-Dpr-OH, N-Boc-L-2,3-diaminopropanoic acid NALPHA-tert-Butoxycbonyl-L-2,3-diaminopropionic acid BOC-L-DAP-OH BOC-L-2,3- DIAMINOPROPIONIC ACID (S)-2-(AMinoMethyl)-4-(tert-butoxy)-4-oxobutanoic acid (S)-3-Amino-2-Boc-propionic acid Boc-Dap-OH(Na-Boc-2,3-DiaMinopropionic acid) 3-Amino-Boc-L-alanine (S)-3-AMINO-2-(TERT-BUTOXYCBONYLAMINO)PROPANOIC ACID 3-[(tert-butoxy)(cbaMoyl)amino]propanoic acid Nalpha-Boc-2,3-diaminopropionic Acid 3-Amino-N-(tert-butoxycbonyl)-L-alanine 3-Amino-N-Boc-L-alanine Boc-Dap-OH Boc-Dpr-OH Nα-BOC-(S)-β-aminoalanine N-ALPHA-TERT-BUTYLOXYCBONYL-L-2,3-DIAMINOPROPIONIC ACID N-T-BOC-BETA-AMINO-L-ALANINE 3-amino-N-(tert-butoxycarbonyl)-L-alanine N-TERT-BOC-BETA-AMINO-L-ALANINE 3-Amino-(tert-butoxycbonyl)-L-alanine, Boc-Dap-OH, Boc-Dpr-OH, (S)-3-Amino-2-(tert-butoxycbonylamino)propanoic acid, Nα-Boc-L-2,3-diaminopropionic acid (Tert-Butoxy)carbonyl Dap-OH N-ALPHA-BOC-(S)-2,3-DIAMINOPROPIONIC ACID (S)-2-[(tert-Butoxycbonyl)amino]-3-aminopropionic acid N-ALPHA-BOC-L-DIAMINOPROPIONIC ACID Nalpha-BOC-beta-Amino-L-alanine, R 3-Amino-N-{[(2-methyl-2-propanyl)oxy]carbonyl}-L-alanine BOC-L-DAPA-OH BOC-DAP-OH N-Boc-beta-amino-L-alanine N-ALPHA-L-(BUTOXYCBONYL)-2,3-DIAMINOPROPIONIC BOC-L-2,3-DIAMINOPROPIONIC ACID NALPHA-BOC-L-BETA-AMINOALANINE L-ALANINE, 3-AMINO-N-[(1,1-DIMETHYLETHOXY)carbonyl] N-ALPHA-BOC-BETA-AMINO-L-ALANINE MFCD00236843 N-alpha-L-(Butoxycbonyl)-2,3-diaMinopropionic aci N(ɑ)-Boc-L-2,3-diaminopropionic acid N-t-BOC-amino-L-alanine Na-Boc-L-2,3-diaminopropionic acid 3-AMINO-(TERT-BUTOXYCBONYL)-L-ALANINE N-ALPHA-BOC-L-2,3-DIAMINOPROPIONIC ACID 3-Amino-(tert-butoxycbonyl)-L-alanine, Boc-Dpr-OH, (S)-3-Amino-2-(tert-butoxycbonylamino)propanoic acid, Nα-Boc-L-2,3-diaminopropionic acid N-ALPHA-T-BUTOXYCBONYL-L-ALPHA,BETA-DIAMINOPROPIONIC ACID BOC-DPR-OH BOC-L-DAP-OH Boc-Dapa-OH N-ALPHA-T-BUTYLOXYCBONYL-L-2,3-DIAMINOPROPIONIC ACID N-BOC-L-2,3-DIAMINOPROPANOIC ACID (S)-3-Amino-Boc-Alanine BOC-ALPHA,BETA-DIAMINOPROPIONIC ACID 3-Amino-Boc-L-alanin BOC-L-ALPHA,BETA-DIAMINOPROPIONIC ACID N-ALPHA-L-(BUTOXYCBONYL)2,3-DIAMINOPROPIONIC ACID N2-tert-Butoxycbonyl-L-2,3-diaminopropionic acid Nα-Boc-L-2,3-diaminopropionic acid (HPLC) N2-tertbutoxycbonyl-L-2,3-diaMinopropanoic acid (n-boc-β-amino)-ala-oh 3-Amino-N-(tert-butoxycbonyl)-L-alanine |
| Description | Boc-L-Dap-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
|---|---|
| Related Catalog |
| Density | 1.2±0.1 g/cm3 |
|---|---|
| Boiling Point | 364.4±37.0 °C at 760 mmHg |
| Melting Point | 210ºC (dec.) |
| Molecular Formula | C8H16N2O4 |
| Molecular Weight | 204.22 |
| Flash Point | 174.2±26.5 °C |
| Exact Mass | 204.111008 |
| PSA | 101.65000 |
| LogP | 0.84 |
| Vapour Pressure | 0.0±1.7 mmHg at 25°C |
| Index of Refraction | 1.489 |
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| Hazard Codes | Xi |
| Safety Phrases | S24/25 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
|
~93%
73259-81-1 |
| Literature: Kucharczyk, N.; Badet, B.; Goffic, F. Le Synthetic Communications, 1989 , vol. 19, # 9-10 p. 1603 - 1610 |
|
~16%
73259-81-1 |
| Literature: Kucharczyk, N.; Badet, B.; Goffic, F. Le Synthetic Communications, 1989 , vol. 19, # 9-10 p. 1603 - 1610 |
| Precursor 1 | |
|---|---|
| DownStream 0 | |