FMOC-N-(N-BETA-BOC-AMINOETHYL)-GLY-OH
- Product Name
- FMOC-N-(N-BETA-BOC-AMINOETHYL)-GLY-OH
- CAS No.
- 141743-15-9
- Chemical Name
- FMOC-N-(N-BETA-BOC-AMINOETHYL)-GLY-OH
- Synonyms
- FMOC-AEG-OH;FMOC-AEG(BOC)-OH;FMOC-BOCNHETGLY-OH;Fmoc-N-(2-Boc-aminoethyl)-Gly-OH;FMOC-N-(2-BOC-AMINOETHYL)-GLYCINE;Fmoc-N-(N-a-Boc-aminoethyl)-Gly-OH;Fmoc-N-(N-β-Boc-aminoethyl)-Gly-OH;FMoc-N-(N-b-Boc-aMinoethyl)-Gly-OH;FMOC-N-(N-BETA-BOC-AMINOETHYL)-GLY-OH;FMOC-N-(N-BETA-BOC-AMINOETHYL)-GLYCINE
- CBNumber
- CB5428715
- Molecular Formula
- C24H28N2O6
- Formula Weight
- 440.49
- MOL File
- 141743-15-9.mol
FMOC-N-(N-BETA-BOC-AMINOETHYL)-GLY-OH Property
- Boiling point:
- 638.3±48.0 °C(Predicted)
- Density
- 1.250±0.06 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- pka
- 3.85±0.10(Predicted)
N-Bromosuccinimide Price
- Product number
- F604393
- Product name
- Fmoc-N-(2-Boc-aminoethyl)-Gly-OH
- Packaging
- 500mg
- Price
- $285
- Updated
- 2021/12/16
- Product number
- FAA1767
- Product name
- Fmoc-Aeg(Boc)-OH
- Packaging
- 1g
- Price
- $168.75
- Updated
- 2021/12/16
- Product number
- AS86257
- Product name
- Fmoc-N-(2-Boc-aminoethyl)glycine
- Purity
- 95+%
- Packaging
- 5G
- Price
- $774
- Updated
- 2021/12/16
- Product number
- AAA0003858
- Product name
- FMOC-N-(2-BOC-AMINOETHYL)-GLY-OH
- Purity
- 95.00%
- Packaging
- 1G
- Price
- $848.93
- Updated
- 2021/12/16
- Product number
- 11190
- Product name
- Fmoc-N-(2-Boc-aminoethyl)glycine,99%(HPLC)
- Purity
- 99%(HPLC)
- Packaging
- 5G
- Price
- $1310.4
- Updated
- 2021/12/16
FMOC-N-(N-BETA-BOC-AMINOETHYL)-GLY-OH Chemical Properties,Usage,Production
Chemical Properties
White crystalline powder
Uses
Fmoc-N-(2-Boc-aminoethyl)-Gly-OH is a Fmoc-protected glycine derivative that can be used in antibody agent coupling (ADC) synthesis. ADC consists of antibodies that are linked to ADC cytotoxins via ADC junctions[1].
Synthesis
82911-69-1
90495-99-1
141743-15-9
The general procedure for the synthesis of Fmoc-N-(2-Boc-aminoethyl)glycine from 9-fluorenylmethyl-N-succinimidyl carbonate and 2-((2-((tert-butoxycarbonyl)amino)ethyl)amino)acetic acid was as follows: 10.9 g (50 mmol) of 2-((2-((tert-butoxycarbonyl)amino)ethyl)amino)acetic acid was mixed and stirred with 50 mL of water, adding 11.3 g (135 mmol) sodium bicarbonate and 50 mL of tetrahydrofuran. Subsequently, 24.3 g (72 mmol) of 9-fluorenylmethyl-N-succinimidyl carbonate was added. The reaction mixture was stirred at room temperature for 20 h. After completion of the reaction, the resulting salt was removed by filtration. The filtrate was acidified to separate the phases and the organic phase was subsequently concentrated to afford the product N-(2-tert-butoxycarbonylaminoethyl)-N-(9-fluorenylmethoxycarbonyl)aminoacetic acid in 21.0 g (99%) yield.
References
[1] Hiroyuki Naito, et al. (anti-her2 antibody)-drug conjugate. EP3130608
FMOC-N-(N-BETA-BOC-AMINOETHYL)-GLY-OH Preparation Products And Raw materials
Raw materials
Preparation Products
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