CAS No.: 175291-56-2 — Fmoc-O-(benzylphospho)-L-threonine (Fmoc-苏氨酸磷酸苄酯)

1. Primary Information

English name:	Fmoc-O-(benzylphospho)-L-threonine
CAS No.:	175291-56-2
Molecular formula:	C₂₆H₂₆NO₈P
Molecular weight:	511.5 g/mol
SMILES:	CC(C(C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13)OP(=O)(O)OCC4=CC=CC=C4
Structural class:
Other identifiers:	-

2. Suppliers & Pricing

Supplier	Pack size	Purity	Price (CNY)	Storage conditions	Lead time	Notes
Kehua Intelligence	5mg	HPLC≥98%	96	2-8℃	in stock	-
Kehua Intelligence	100mg	95%	96	2-8℃	in stock	-
Kehua Intelligence	250mg	95%	160	2-8℃	in stock	-
Kehua Intelligence	1g	95%	480	2-8℃	in stock	-
Kehua Intelligence	5g	95%	1600	2-8℃	in stock	-
Kehua Intelligence	25g	95%	4800	2-8℃	in stock	-

3. Structures

3.1 2D structure

3.2 3D structure

-1 -2 -3 62 65 0 1 0 0 0 0 0999 V2000 -3.3593 -1.6790 1.6014 P 0 0 1 0 0 0 0 0 0 0 0 0 2.5980 -1.1235 -0.7469 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.1772 -1.8340 0.5118 O 0 0 0 0 0 0 0 0 0 0 0 0 2.2388 -3.1657 -1.7346 O 0 0 0 0 0 0 0 0 0 0 0 0 -4.0380 -0.2444 1.2817 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.5827 -3.9139 -2.6514 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.3691 -1.6605 -2.4893 O 0 0 0 0 0 0 0 0 0 0 0 0 -4.4551 -2.7578 1.0961 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.9282 -1.8656 3.0278 O 0 0 0 0 0 0 0 0 0 0 0 0 0.5649 -2.0855 -0.5459 N 0 0 0 0 0 0 0 0 0 0 0 0 4.6127 0.1602 -0.7655 C 0 0 0 0 0 0 0 0 0 0 0 0 3.8475 1.4097 -1.1776 C 0 0 0 0 0 0 0 0 0 0 0 0 4.6368 0.3031 0.7496 C 0 0 0 0 0 0 0 0 0 0 0 0 3.4980 2.1713 -0.0396 C 0 0 0 0 0 0 0 0 0 0 0 0 3.9824 1.4923 1.1429 C 0 0 0 0 0 0 0 0 0 0 0 0 3.9319 -1.1234 -1.2236 C 0 0 0 0 0 0 0 0 0 0 0 0 3.5139 1.8310 -2.4547 C 0 0 0 0 0 0 0 0 0 0 0 0 5.2085 -0.5454 1.6838 C 0 0 0 0 0 0 0 0 0 0 0 0 2.8006 3.3608 -0.1741 C 0 0 0 0 0 0 0 0 0 0 0 0 3.8879 1.8356 2.4818 C 0 0 0 0 0 0 0 0 0 0 0 0 2.8109 3.0295 -2.5896 C 0 0 0 0 0 0 0 0 0 0 0 0 5.1131 -0.1990 3.0328 C 0 0 0 0 0 0 0 0 0 0 0 0 2.4570 3.7866 -1.4606 C 0 0 0 0 0 0 0 0 0 0 0 0 4.4585 0.9794 3.4280 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.4783 -3.0713 -0.7117 C 0 0 1 0 0 0 0 0 0 0 0 0 -1.4835 -3.0791 0.4443 C 0 0 1 0 0 0 0 0 0 0 0 0 1.8332 -2.2171 -1.0711 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.8282 -3.3504 1.7933 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.1652 -2.7781 -2.0330 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.4866 0.0523 -0.0296 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.0688 1.4350 -0.0471 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.2494 2.5238 -0.3241 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.4225 1.6154 0.2145 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.7908 3.8092 -0.3399 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.9638 2.9009 0.1985 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.1480 3.9977 -0.0786 C 0 0 0 0 0 0 0 0 0 0 0 0 5.6390 0.2230 -1.1462 H 0 0 0 0 0 0 0 0 0 0 0 0 3.9255 -1.1764 -2.3191 H 0 0 0 0 0 0 0 0 0 0 0 0 4.4632 -2.0002 -0.8343 H 0 0 0 0 0 0 0 0 0 0 0 0 3.7889 1.2519 -3.3292 H 0 0 0 0 0 0 0 0 0 0 0 0 5.7188 -1.4538 1.3831 H 0 0 0 0 0 0 0 0 0 0 0 0 2.5221 3.9575 0.6880 H 0 0 0 0 0 0 0 0 0 0 0 0 3.3874 2.7431 2.8024 H 0 0 0 0 0 0 0 0 0 0 0 0 2.5345 3.3832 -3.5794 H 0 0 0 0 0 0 0 0 0 0 0 0 5.5511 -0.8470 3.7874 H 0 0 0 0 0 0 0 0 0 0 0 0 1.9100 4.7167 -1.5905 H 0 0 0 0 0 0 0 0 0 0 0 0 4.3970 1.2284 4.4843 H 0 0 0 0 0 0 0 0 0 0 0 0 0.0076 -4.0518 -0.7925 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.2219 -3.8648 0.2429 H 0 0 0 0 0 0 0 0 0 0 0 0 0.3422 -1.2242 -0.0557 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.5526 -3.7421 2.5130 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0522 -4.1184 1.7017 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.3754 -2.4483 2.2177 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.2371 -0.6834 -0.3394 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.6484 -0.0195 -0.7318 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.0454 -3.7216 -3.4948 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.2192 -2.9637 1.6756 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.1907 2.3884 -0.5269 H 0 0 0 0 0 0 0 0 0 0 0 0 -7.0666 0.7682 0.4337 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.1555 4.6634 -0.5550 H 0 0 0 0 0 0 0 0 0 0 0 0 -8.0204 3.0479 0.4026 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.5694 4.9986 -0.0907 H 0 0 0 0 0 0 0 0 0 0 0 0 1 3 1 0 0 0 0 1 5 1 0 0 0 0 1 8 1 0 0 0 0 1 9 2 0 0 0 0 2 16 1 0 0 0 0 2 27 1 0 0 0 0 3 26 1 0 0 0 0 4 27 2 0 0 0 0 5 30 1 0 0 0 0 6 29 1 0 0 0 0 6 56 1 0 0 0 0 7 29 2 0 0 0 0 8 57 1 0 0 0 0 10 25 1 0 0 0 0 10 27 1 0 0 0 0 10 50 1 0 0 0 0 11 12 1 0 0 0 0 11 13 1 0 0 0 0 11 16 1 0 0 0 0 11 37 1 0 0 0 0 12 14 1 0 0 0 0 12 17 2 0 0 0 0 13 15 1 0 0 0 0 13 18 2 0 0 0 0 14 15 1 0 0 0 0 14 19 2 0 0 0 0 15 20 2 0 0 0 0 16 38 1 0 0 0 0 16 39 1 0 0 0 0 17 21 1 0 0 0 0 17 40 1 0 0 0 0 18 22 1 0 0 0 0 18 41 1 0 0 0 0 19 23 1 0 0 0 0 19 42 1 0 0 0 0 20 24 1 0 0 0 0 20 43 1 0 0 0 0 21 23 2 0 0 0 0 21 44 1 0 0 0 0 22 24 2 0 0 0 0 22 45 1 0 0 0 0 23 46 1 0 0 0 0 24 47 1 0 0 0 0 25 26 1 0 0 0 0 25 29 1 0 0 0 0 25 48 1 0 0 0 0 26 28 1 0 0 0 0 26 49 1 0 0 0 0 28 51 1 0 0 0 0 28 52 1 0 0 0 0 28 53 1 0 0 0 0 30 31 1 0 0 0 0 30 54 1 0 0 0 0 30 55 1 0 0 0 0 31 32 2 0 0 0 0 31 33 1 0 0 0 0 32 34 1 0 0 0 0 32 58 1 0 0 0 0 33 35 2 0 0 0 0 33 59 1 0 0 0 0 34 36 2 0 0 0 0 34 60 1 0 0 0 0 35 36 1 0 0 0 0 35 61 1 0 0 0 0 36 62 1 0 0 0 0

4. International Nomenclature & Identifiers

4.1 IUPAC Name

(2S,3R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-[hydroxy(phenylmethoxy)phosphoryl]oxybutanoic acid

4.2 InChI

InChI=1S/C26H26NO8P/c1-17(35-36(31,32)34-15-18-9-3-2-4-10-18)24(25(28)29)27-26(30)33-16-23-21-13-7-5-11-19(21)20-12-6-8-14-22(20)23/h2-14,17,23-24H,15-16H2,1H3,(H,27,30)(H,28,29)(H,31,32)/t17-,24+/m1/s1

4.3 InChIKey

HOFDVXHILSPFNS-OSPHWJPCSA-N

4.4 Canonical SMILES

CC(C(C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13)OP(=O)(O)OCC4=CC=CC=C4

4.5 Isomeric SMILES

C[C@H]([C@@H](C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13)OP(=O)(O)OCC4=CC=CC=C4

4.6 SDF file

Coming soon

5. Spectroscopic data

5.1 ¹³C nuclear magnetic resonance (¹³C NMR)

5.2 ¹H nuclear magnetic resonance (¹H NMR)

5.3 Mass spectrometry (MS)

Coming soon

5.4 Infrared spectroscopy (IR)

Coming soon

5.5 Ultraviolet/visible spectroscopy (UV/Vis)

Coming soon

1. Primary Information

2. Suppliers & Pricing

3. Structures

3.1 2D structure

3.2 3D structure

4. International Nomenclature & Identifiers

4.1 IUPAC Name

4.2 InChI

4.3 InChIKey

4.4 Canonical SMILES

4.5 Isomeric SMILES

4.6 SDF file

5. Spectroscopic data

5.1 13C nuclear magnetic resonance (13C NMR)

5.2 1H nuclear magnetic resonance (1H NMR)

5.3 Mass spectrometry (MS)

5.4 Infrared spectroscopy (IR)

5.5 Ultraviolet/visible spectroscopy (UV/Vis)

5.1 ¹³C nuclear magnetic resonance (¹³C NMR)

5.2 ¹H nuclear magnetic resonance (¹H NMR)