CAS No.: 87531-10-0 — (2R,3S,5R)-5-(5-((E)-2-bromovinyl)-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2-(((4-chlorobenzoyl)oxy)methyl)tetrahydrofuran-3-yl 4-chlorobenzoate (Uridine, 5-(2-bromoethenyl)-2'-deoxy-, 3',5'-bis(4-chlorobenzoate), (E)-)

1. Primary Information

English name:	(2R,3S,5R)-5-(5-((E)-2-bromovinyl)-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2-(((4-chlorobenzoyl)oxy)methyl)tetrahydrofuran-3-yl 4-chlorobenzoate
CAS No.:	87531-10-0
Molecular formula:	C₂₅H₁₉BRCl₂N₂O₇
Molecular weight:	610.2 g/mol
SMILES:	C1C(C(OC1N2C=C(C(=O)NC2=O)C=CBr)COC(=O)C3=CC=C(C=C3)Cl)OC(=O)C4=CC=C(C=C4)Cl
Structural class:
Other identifiers:	-

2. Suppliers & Pricing

Supplier	Pack size	Purity	Price (CNY)	Storage conditions	Lead time	Notes
Kehua Intelligence	100mg	98%	1616	-20℃	in stock	-
Kehua Intelligence	250mg	98%	2712	-20℃	in stock	-
Kehua Intelligence	500mg	98%	3520	-20℃	in stock	-

3. Structures

3.1 2D structure

3.2 3D structure

-1 -2 -3 56 59 0 1 0 0 0 0 0999 V2000 -5.9926 -0.8200 -0.7562 Br 0 0 0 0 0 0 0 0 0 0 0 0 9.0666 1.3498 1.8979 Cl 0 0 0 0 0 0 0 0 0 0 0 0 -6.2474 4.6324 2.5215 Cl 0 0 0 0 0 0 0 0 0 0 0 0 0.3206 -0.4712 0.4790 O 0 0 0 0 0 0 0 0 0 0 0 0 3.1399 -0.0910 -0.6521 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.3671 1.4781 -0.6191 O 0 0 0 0 0 0 0 0 0 0 0 0 1.1316 -4.4544 1.0577 O 0 0 0 0 0 0 0 0 0 0 0 0 3.6121 1.6739 -2.0528 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.3347 -5.3659 0.4857 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.7454 1.7153 -2.4476 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.2437 -2.7337 0.2858 N 0 0 0 0 0 0 0 0 0 0 0 0 -1.1005 -4.8903 0.7664 N 0 0 0 0 0 0 0 0 0 0 0 0 1.8832 -0.2927 -1.2951 C 0 0 2 0 0 0 0 0 0 0 0 0 0.7880 0.4409 -0.5336 C 0 0 1 0 0 0 0 0 0 0 0 0 1.4744 -1.7423 -1.1707 C 0 0 0 0 0 0 0 0 0 0 0 0 0.8279 -1.7847 0.2043 C 0 0 1 0 0 0 0 0 0 0 0 0 -0.3988 0.8121 -1.4133 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.5322 -2.3535 -0.0696 C 0 0 0 0 0 0 0 0 0 0 0 0 0.0158 -4.0486 0.7263 C 0 0 0 0 0 0 0 0 0 0 0 0 3.9098 0.9302 -1.1310 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.6018 -3.1595 -0.0309 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.4050 -4.5652 0.4242 C 0 0 0 0 0 0 0 0 0 0 0 0 5.1871 1.0337 -0.3811 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.4998 1.8794 -1.2626 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.9130 -2.7024 -0.4137 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.4276 2.5615 -0.3254 C 0 0 0 0 0 0 0 0 0 0 0 0 6.1164 2.0174 -0.7192 C 0 0 0 0 0 0 0 0 0 0 0 0 5.4574 0.1479 0.6618 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.3112 -1.4373 -0.2720 C 0 0 0 0 0 0 0 0 0 0 0 0 7.3162 2.1152 -0.0146 C 0 0 0 0 0 0 0 0 0 0 0 0 6.6571 0.2455 1.3665 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.6492 3.0519 -0.7870 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.0781 2.7115 1.0166 C 0 0 0 0 0 0 0 0 0 0 0 0 7.5866 1.2291 1.0283 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.5211 3.6924 0.0933 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.9500 3.3521 1.8970 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.1715 3.8424 1.4353 C 0 0 0 0 0 0 0 0 0 0 0 0 1.9446 -0.0026 -2.3502 H 0 0 0 0 0 0 0 0 0 0 0 0 1.1607 1.3300 -0.0131 H 0 0 0 0 0 0 0 0 0 0 0 0 2.3093 -2.4463 -1.2449 H 0 0 0 0 0 0 0 0 0 0 0 0 0.7496 -1.9931 -1.9547 H 0 0 0 0 0 0 0 0 0 0 0 0 1.5826 -2.0050 0.9686 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0600 1.4941 -2.2028 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.8475 -0.0646 -1.8901 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.6428 -1.3360 -0.4073 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.9371 -5.8429 1.0803 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.5877 -3.4424 -0.8359 H 0 0 0 0 0 0 0 0 0 0 0 0 5.9246 2.7172 -1.5282 H 0 0 0 0 0 0 0 0 0 0 0 0 4.7616 -0.6321 0.9579 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.7028 -0.6546 0.1624 H 0 0 0 0 0 0 0 0 0 0 0 0 8.0311 2.8866 -0.2889 H 0 0 0 0 0 0 0 0 0 0 0 0 6.8549 -0.4514 2.1771 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.9404 2.9441 -1.8285 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.1381 2.3439 1.4182 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.4700 4.0689 -0.2801 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.6651 3.4618 2.9402 H 0 0 0 0 0 0 0 0 0 0 0 0 1 29 1 0 0 0 0 2 34 1 0 0 0 0 3 37 1 0 0 0 0 4 14 1 0 0 0 0 4 16 1 0 0 0 0 5 13 1 0 0 0 0 5 20 1 0 0 0 0 6 17 1 0 0 0 0 6 24 1 0 0 0 0 7 19 2 0 0 0 0 8 20 2 0 0 0 0 9 22 2 0 0 0 0 10 24 2 0 0 0 0 11 16 1 0 0 0 0 11 18 1 0 0 0 0 11 19 1 0 0 0 0 12 19 1 0 0 0 0 12 22 1 0 0 0 0 12 46 1 0 0 0 0 13 14 1 0 0 0 0 13 15 1 0 0 0 0 13 38 1 0 0 0 0 14 17 1 0 0 0 0 14 39 1 0 0 0 0 15 16 1 0 0 0 0 15 40 1 0 0 0 0 15 41 1 0 0 0 0 16 42 1 0 0 0 0 17 43 1 0 0 0 0 17 44 1 0 0 0 0 18 21 2 0 0 0 0 18 45 1 0 0 0 0 20 23 1 0 0 0 0 21 22 1 0 0 0 0 21 25 1 0 0 0 0 23 27 2 0 0 0 0 23 28 1 0 0 0 0 24 26 1 0 0 0 0 25 29 2 0 0 0 0 25 47 1 0 0 0 0 26 32 2 0 0 0 0 26 33 1 0 0 0 0 27 30 1 0 0 0 0 27 48 1 0 0 0 0 28 31 2 0 0 0 0 28 49 1 0 0 0 0 29 50 1 0 0 0 0 30 34 2 0 0 0 0 30 51 1 0 0 0 0 31 34 1 0 0 0 0 31 52 1 0 0 0 0 32 35 1 0 0 0 0 32 53 1 0 0 0 0 33 36 2 0 0 0 0 33 54 1 0 0 0 0 35 37 2 0 0 0 0 35 55 1 0 0 0 0 36 37 1 0 0 0 0 36 56 1 0 0 0 0

4. International Nomenclature & Identifiers

4.1 IUPAC Name

[(2R,3S,5R)-5-[5-[(E)-2-bromoethenyl]-2,4-dioxopyrimidin-1-yl]-3-(4-chlorobenzoyl)oxyoxolan-2-yl]methyl 4-chlorobenzoate

4.2 InChI

InChI=1S/C25H19BrCl2N2O7/c26-10-9-16-12-30(25(34)29-22(16)31)21-11-19(37-24(33)15-3-7-18(28)8-4-15)20(36-21)13-35-23(32)14-1-5-17(27)6-2-14/h1-10,12,19-21H,11,13H2,(H,29,31,34)/b10-9+/t19-,20+,21+/m0/s1

4.3 InChIKey

ODZHXZBXXUFBMH-JQTKOYJDSA-N

4.4 Canonical SMILES

C1C(C(OC1N2C=C(C(=O)NC2=O)C=CBr)COC(=O)C3=CC=C(C=C3)Cl)OC(=O)C4=CC=C(C=C4)Cl

4.5 Isomeric SMILES

C1[C@@H]([C@H](O[C@H]1N2C=C(C(=O)NC2=O)/C=C/Br)COC(=O)C3=CC=C(C=C3)Cl)OC(=O)C4=CC=C(C=C4)Cl

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)

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)