FMOC-ALA-ALDEHYDE
- Product Name
- FMOC-ALA-ALDEHYDE
- CAS No.
- 146803-41-0
- Chemical Name
- FMOC-ALA-ALDEHYDE
- Synonyms
- Fmoc-Ala-CHO;FMOC-ALA-ALDEHYDE;(S)-2-(Fmoc-amino)propanal;(9H-Fluoren-9-yl)MethOxy]Carbonyl Ala-aldehyde;(S)-(9H-fluoren-9-yl)methyl 1-oxopropan-2-ylcarbamate;(9H-fluoren-9-yl)methyl N-[(2S)-1-oxopropan-2-yl]carbamate;Carbamic acid, N-[(1S)-1-methyl-2-oxoethyl]-, 9H-fluoren-9-ylmethyl ester
- CBNumber
- CB4342182
- Molecular Formula
- C18H17NO3
- Formula Weight
- 295.33
- MOL File
- 146803-41-0.mol
FMOC-ALA-ALDEHYDE Property
- Boiling point:
- 479.9±28.0 °C(Predicted)
- Density
- 1.203±0.06 g/cm3(Predicted)
- storage temp.
- Inert atmosphere,Store in freezer, under -20°C
- pka
- 10.80±0.46(Predicted)
- Appearance
- White to off-white Solid
- optical activity
- 42.401 °(C=1.0 g/100ml, CHCL3)
N-Bromosuccinimide Price
- Product number
- F594905
- Product name
- Fmoc-ala-aldehyde
- Packaging
- 100mg
- Price
- $70
- Updated
- 2021/12/16
- Product number
- AAA0006774
- Product name
- FMOC-ALA-ALDEHYDE
- Purity
- 95.00%
- Packaging
- 250MG
- Price
- $656
- Updated
- 2021/12/16
- Product number
- AAA0006774
- Product name
- FMOC-ALA-ALDEHYDE
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $497.6
- Updated
- 2021/12/16
- Product number
- V3382
- Product name
- Fmoc-ala-aldehyde
- Packaging
- 10g
- Price
- $1743
- Updated
- 2021/12/16
- Product number
- A246654
- Product name
- (S)-(9H-Fluoren-9-yl)methyl(1-oxopropan-2-yl)carbamate
- Purity
- 97%
- Packaging
- 100mg
- Price
- $51
- Updated
- 2021/12/16
FMOC-ALA-ALDEHYDE Chemical Properties,Usage,Production
Uses
Fmoc-ala-aldehyde acts as an intermediate in the synthesis of α-amino aldehydes and peptide aldehydes.
Synthesis
161529-13-1
146803-41-0
To an anhydrous dichloromethane (10 mL) solution of oxalyl chloride (1.89 g, 15.0 mmol) was added anhydrous dichloromethane (10 mL) solution of dimethyl sulfoxide (1.2 g, 15.0 mmol) dropwise at -65 °C. After stirring for 30 minutes, anhydrous dichloromethane (20 mL) solution of N-fluorenylmethoxycarbonyl-L-alaninol (3.0 g, 10.0 mmol) was added slowly dropwise. After continued stirring for 2 h, triethylamine (3.0 g, 30 mmol) was added dropwise, followed by gradual warming of the reaction mixture to room temperature. Upon completion of the reaction, the reaction was quenched with water and extracted with dichloromethane (3 x 100 mL). The organic phases were combined, washed with saturated brine and dried over anhydrous sodium sulfate. After filtration, the solvent was removed by concentration under reduced pressure to give the white solid product methyl (S)-(9H-fluoren-9-yl)methyl(1-oxopropan-2-yl)carbamate (2.8 g, 94.9% yield).
References
[1] Patent: WO2011/69063, 2011, A2. Location in patent: Page/Page column 82
[2] Synthetic Communications, 2007, vol. 37, # 20, p. 3493 - 3499
[3] Tetrahedron Letters, 2000, vol. 41, # 32, p. 6131 - 6135
[4] Tetrahedron Letters, 2000, vol. 41, # 9, p. 1359 - 1362
[5] Journal of Medicinal Chemistry, 2007, vol. 50, # 23, p. 5627 - 5643
FMOC-ALA-ALDEHYDE Preparation Products And Raw materials
Raw materials
Preparation Products
FMOC-ALA-ALDEHYDE Suppliers
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