C30H30N2O8 URIDINE, 5'-O- [BIS (4-Movhyphenyl) phenylmethyl] - (9ci, aci)

vokatra

C30H30N2O8 URIDINE, 5'-O- [BIS (4-Movhyphenyl) phenylmethyl] - (9ci, aci)

Fampahalalana fototra:


Ny antsipiriany momba ny vokatra

Product Tags

Toetra ara-batana

Fananana ara-batana lehibe sarobidy toe-javatra
Lanjan'ny molekiola 546.57 -
Melting Point (fanandramana) 111-112 ° C Solvent: Ethyl acetate
Fahalemena (nambara) 1.343 ± 0.06 g / cm3 Temp: 20 ° C; Press: 760 Torr
PKA (nambara) 9.39 ± 0.10 Ankamaroan'ny temps temp: 25 ° C

Anarana sy mpanabe hafa

Canonical Smiles O = C1C = CN (C (= O) N1) CCOC (COC (C = 3C = CC = CC3) (CC3) C = C (OC) C = C (OC) C = C5) C (OC) C = C5) C (O) C2O)
Isomeric Smiles C (OC [C @ h] 1o [C @ h] ([O) (O)
Inchi
Inchi = 1s / c30h30n2o8 / c1-37-22-12-8-20 (9-13-22) 30 (19-6-4-3-5-7-19,71-19,21-19,21-19-13 (38-2) 15-11-21) 39-18-24-26 (34) 27 (35) 28 (40-24)
17-16-25 (33) 31-29 (32) 36 / H3-17.24,26-28,34-35-28,34-35H, 18H2,1-23, (H, 31,3336) / T24-, 26- / M1 / ​​S1
Inchi Key
Pcfsnqyxxacuhm-yuloidqlsa-n
4 anarana hafa ho an'ity akora ity
5'-O- [bis (4-metoxyphenyl) phenylmethethyl] Uridine (Aci); Uridine, 5'-O- [α, α-bis (p-metoxyphenyl) benzyl] - (7ci); 5'-imethoHobytrityl Uridine; 5'-o- (4,4'-dimethoxytrityl) uridine

Fanandramana

Fananana misy
mafana

mafana

NY FANANANA sarobidy toe-javatra

Source

Melting Point 122-123 ° C    

(1) Cas

Melting Point 111-112 ° C Solvent: EtaiL Acetate

(2) Cas

Melting Point Jereo ny lahatsoratra feno    

(3) Cas

(1) Zekri, Negar; Bulletin ny fiaraha-monina simika ao Etiopia, (2010), 24 (2), 299-304, caplus

(2) Patil, Premanand Ramrao; Journal of Carbohydrate Chemistry, (2008), 27 (5), 279-293, Caplus

(3) Khalafi-Nefhad, Ali; Tetters Tetrahe, (2004), 45 (36), 6737-6739, Caplus

Spectrimal spectra

Spectra misy
1H NMR
13c NMR
-bahoaka

Ny fananana mialoha

Fananana misy
niteraka
simika
hakitroky
Lipinski
Mifandraika mifandraika

niteraka

NY FANANANA sarobidy toe-javatra Source
Factor Bioconcentration 904 PH 1; Temp: 25 ° C (1) ACD
Factor Bioconcentration 904 PH 2; Temp: 25 ° C (1) ACD
Factor Bioconcentration 904 PH 3; Temp: 25 ° C (1) ACD
Factor Bioconcentration 904 PH 4; Temp: 25 ° C (1) ACD
Factor Bioconcentration 904 PH 5; Temp: 25 ° C (1) ACD
Factor Bioconcentration 904 PH 6; Temp: 25 ° C (1) ACD
Factor Bioconcentration 900 PH 7; Temp: 25 ° C (1) ACD
Factor Bioconcentration 861 PH 8; Temp: 25 ° C (1) ACD
Factor Bioconcentration 602 PH 9; Temp: 25 ° C (1) ACD

 

NY FANANANA sarobidy toe-javatra Source
Factor Bioconcentration 156 PH 10; Temp: 25 ° C (1) ACD

(1) kajy amin'ny fampandrosoana ny simika Advanced (ACD / Labs) rindrambaiko V11.02 (© 1994-2023 ACD / Labs)

simika

NY FANANANA sarobidy toe-javatra Source
Koc 4550 PH 1; Temp: 25 ° C (1) ACD
Koc 4550 PH 2; Temp: 25 ° C (1) ACD
Koc 4550 PH 3; Temp: 25 ° C (1) ACD
Koc 4550 PH 4; Temp: 25 ° C (1) ACD
Koc 4550 PH 5; Temp: 25 ° C (1) ACD
Koc 4540 PH 6; Temp: 25 ° C (1) ACD
Koc 4520 PH 7; Temp: 25 ° C (1) ACD
Koc 4330 PH 8; Temp: 25 ° C (1) ACD
Koc 3030 PH 9; Temp: 25 ° C (1) ACD
Koc 785 PH 10; Temp: 25 ° C (1) ACD
LogD 4.19 PH 1; Temp: 25 ° C (1) ACD
LogD 4.19 PH 2; Temp: 25 ° C (1) ACD
LogD 4.19 PH 3; Temp: 25 ° C (1) ACD
LogD 4.19 PH 4; Temp: 25 ° C (1) ACD
LogD 4.19 PH 5; Temp: 25 ° C (1) ACD
LogD 4.19 PH 6; Temp: 25 ° C (1) ACD
LogD 4.19 PH 7; Temp: 25 ° C (1) ACD
LogD 4.17 PH 8; Temp: 25 ° C (1) ACD
LogD 4.02 PH 9; Temp: 25 ° C (1) ACD
LogD 3.43 PH 10; Temp: 25 ° C (1) ACD
Logp 4.192 ± 0.628 Temp: 25 ° C (1) ACD
Solondrailala an-tsokosoko 3.2 x 10-4 g / l Temp: 25 ° C (1) ACD
Supubility Mass 3.2 x 10-4 g / l PH 1; Temp: 25 ° C (1) ACD
Supubility Mass 3.2 x 10-4 g / l PH 2; Temp: 25 ° C (1) ACD
Supubility Mass 3.2 x 10-4 g / l PH 3; Temp: 25 ° C (1) ACD
Supubility Mass 3.2 x 10-4 g / l PH 4; Temp: 25 ° C (1) ACD
Supubility Mass 3.2 x 10-4 g / l PH 5; Temp: 25 ° C (1) ACD
Supubility Mass 3.2 x 10-4 g / l PH 6; Temp: 25 ° C (1) ACD
Supubility Mass 3.2 x 10-4 g / l PH 7; Temp: 25 ° C (1) ACD

 

NY FANANANA sarobidy toe-javatra Source
Supubility Mass 3.3 x 10-4 g / l PH 8; Temp: 25 ° C (1) ACD
Supubility Mass 4.8 x 10-4 g / l PH 9; Temp: 25 ° C (1) ACD
Supubility Mass 1.9 x 10-3 g / l PH 10; Temp: 25 ° C (1) ACD
Supubility Mass 3.2 x 10-4 g / l Rano tsy voaroy 6,99; Temp: 25 ° C (1) ACD
Movra intrinsic solubility 5.8 x 10-7 mol / l Temp: 25 ° C (1) ACD
Molar Solubility 5.8 x 10-7 mol / l PH 1; Temp: 25 ° C (1) ACD
Molar Solubility 5.8 x 10-7 mol / l PH 2; Temp: 25 ° C (1) ACD
Molar Solubility 5.8 x 10-7 mol / l PH 3; Temp: 25 ° C (1) ACD
Molar Solubility 5.8 x 10-7 mol / l PH 4; Temp: 25 ° C (1) ACD
Molar Solubility 5.8 x 10-7 mol / l PH 5; Temp: 25 ° C (1) ACD
Molar Solubility 5.8 x 10-7 mol / l PH 6; Temp: 25 ° C (1) ACD
Molar Solubility 5.8 x 10-7 mol / l PH 7; Temp: 25 ° C (1) ACD
Molar Solubility 6.1 X 10-7 mol / l PH 8; Temp: 25 ° C (1) ACD
Molar Solubility 8.7 x 10-7 mol / l PH 9; Temp: 25 ° C (1) ACD
Molar Solubility 3.4 x 10-6 Mol / l PH 10; Temp: 25 ° C (1) ACD
Molar Solubility 5.8 x 10-7 mol / l Rano tsy voaroy 6,99; Temp: 25 ° C (1) ACD
Lanjan'ny molekiola 546.57    
pka 9.39 ± 0.10 Ankamaroan'ny temps temp: 25 ° C (1) ACD

(1) kajy amin'ny fampandrosoana ny simika Advanced (ACD / Labs) rindrambaiko V11.02 (© 1994-2023 ACD / Labs)

hakitroky

NY FANANANA sarobidy toe-javatra Source
hakitroky 1.343 ± 0.06 g / cm3 Temp: 20 ° C; Press: 760 Torr (1) ACD
Molar volume 406.9 ± 3.0 cm3 / mol Temp: 20 ° C; Press: 760 Torr (1) ACD

(1) kajy amin'ny fampandrosoana ny simika Advanced (ACD / Labs) rindrambaiko V11.02 (© 1994-2023 ACD / Labs)

Lipinski

NY FANANANA sarobidy toe-javatra Source
Fatorana rotatateble malalaka 11   (1) ACD
H Mpanaja 10   (1) ACD
H mpamatsy vola 3   (1) ACD
H Donor / Accas Sum 13   (1) ACD
Logp 4.192 ± 0.628 Temp: 25 ° C (1) ACD
 

 

NY FANANANA sarobidy

toe-javatra

Source
Lanjan'ny molekiola 546.57

(1) kajy amin'ny fampandrosoana ny simika Advanced (ACD / Labs) rindrambaiko V11.02 (© 1994-2023 ACD / Labs)

Mifandraika mifandraika

NY FANANANA sarobidy

toe-javatra

Source
Faritra misy polar 127 A2 (1) ACD

(1) kajy amin'ny fampandrosoana ny simika Advanced (ACD / Labs) rindrambaiko V11.02 (© 1994-2023 ACD / Labs)

Pressed spectra

Spectra misy
1H NMR
13c NMR


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