NUMMORSIUT Monomers

NUMMORSIUT Monomers

  • C31h32n2o8 Uridine, 5'-o- [4-Methodyphyl) Phenylmthyl] -2'-o-Methyl- (9c

    C31h32n2o8 Uridine, 5'-o- [4-Methodyphyl) Phenylmthyl] -2'-o-Methyl- (9c

    Kierperlech Eegeschafte Schlëssel kierperlech Eegeschafte Wäerter morkular Gewiicht 560.60.60.60.60.65 ± 0 ° CM3 Press: 760 Torr pka (virausgesot) 9,39 ± 0,10 Tempo) c5 = cc = c (oc) c & £ C2oC = C2C; C2C; C2C ISOM = C (oc) c = C3) 1o [c @ h] ([c @ h] c = c4) C5 = CC = CC = C2C = C2C = C2c = C2C = C2C = C2C = C2 Inchi = 1s / c31h32n2o8 / C1-37-23-13-9-2 ...
  • Cheylethoxy] Methyl] -2,38, 9A-Tetraholy-3-Hydroxy-, 3r, 3r, 3r, 3-.. ( ACI)

    Cheylethoxy] Methyl] -2,38, 9A-Tetraholy-3-Hydroxy-, 3r, 3r, 3r, 3-.. ( ACI)

    Physikalesch Eegeschafte Schlëssel kierperlech Eegeschafte Wäerter morizal Gewiichtsgewiicht 528.55 - Schmelzpunkt (experimentell) 12,10.2 → Virbereedung Press: 760 Torr pka (virausgesot) 12.51 = CC = CC4) (C5 = CC = OC) C = C2C3C (C2OC = C2OC = C2OC = C2OC = C2OC = C2C; C2OC = C2OC = C2OC = C2C; C6C C (OC [C @ h] 1o [C @@] 2 ([C @] ([C @@@ H] 1o) (OC = 3n2 ...
  • C36H39n5o8 Guanoosin, 5'-o- [4-Methodylyl) Phenylylylyl] -2'-O-methyl-

    C36H39n5o8 Guanoosin, 5'-o- [4-Methodylyl) Phenylylylyl] -2'-O-methyl-

    Kierperlech Eegeschafte Schlëssel kierperlech Eegeschafte Wäerter morkulär Gewiicht 669.172 - Dicht (Virbereedung) 1. CM3 CRP: 20 ° ROP: 20 ° CM3 Press: 760 Torr pka (virausgesot) 9.16 ± 0,20 Tempo Tempo Tempo: 25 ° Cann a Identifizéierer O = c1n = c (nc (= o) c (c) c) nc2 = cn2c3oc (CC = 4C = CC = CC4) C3 = CC4) CC = CC4) CNATR C (oc | c @ h] 1o [c4) (c5 = cc = c (oc) c = c5) c6 = cc = cc = cc = cc = cc = cc = cc = cc = C%)
  • C15h21n5o6 Guanosin, 2''-o-methyl-n- (2-methyl-1-oxopropyl) - (9ci, Acri)

    C15h21n5o6 Guanosin, 2''-o-methyl-n- (2-methyl-1-oxopropyl) - (9ci, Acri)

    Kierperlech Eegeschafte Schlëssel kierperlech Eegeschafte Wäerter Bedeitendmordkondulär Gewiicht 367.36 - Dicht (68 g / cm3 cmp: Dréckt: 760 Torr pka (virausgesot) 9.16 ± 0,20 Tempo Tempo Tempo: 25 ° CA an Identifizéierer laachen O (c) [c @ h] 1 [c h] (n2c3 = c (n = c2) c (= o) n = n (c (c (c (c (c) 1 Inchi = 1s / c15h21n5o6 / C1-6 (2) 12 (23) 18-15-17-17--- (13) 19-15) 2 (2-50) 14.00) 14.00) 14.00) 14.00) 14.00) 14.00
  • C39h37n5o7 ANONOSIN, N-Benzoyl-5'-O- [4-Methodyphyl) Phenylmthyl] -2 'O -2'-

    C39h37n5o7 ANONOSIN, N-Benzoyl-5'-O- [4-Methodyphyl) Phenylmthyl] -2 'O -2'-

    Kierperlech Eegeschafte Schlëssel kierperlech Eegeschafte Wäerter Bedeelegung marlecular Gewiicht 687.74 - Dicht (virausgesot) 1.32 ± 0 ° ROPS: Press: 760 Torr pka (virausgesot) 7.87 ± 0,43 meescht sauer Tempo Tempo: 25 ° Cann a Identifizéierer O=C(NC1=NC=NC2=C1N=CN2C3OC(COC(C=4C=CC=CC4)(C5=CC=C(OC)C=C5)C6=CC=C(OC)C=C6)C(O)C3OC)C=7C=CC=CC7 Isomeric SMILES C (oc [cn3) 1o [cc = c (oc) c = c5) (c6 = cc = c (oc) cc = CC = CC = CC = CC = CC = CC = CC = CC = CC = CC = CC = CC = CC = C4) N = CN3) 1 M. (OC @ H = C5) (C6 = CC = C2) C1) C7 = CC = CC = CC = CC = CC = CC = CC = CC = CC = CC = CC = C4) N = CN3) (C.
  • C13h19n5o6 Guanosin, 2 '-o- (2-Methohyethyl) - (9Cci, Aci)

    C13h19n5o6 Guanosin, 2 '-o- (2-Methohyethyl) - (9Cci, Aci)

    Stoff Detail Cas Registry Nummer 473278-54 Tasteier kierperlech Eegeschafte Wäertkonditulaire Wuelbestänn Press: 760 Torr pka (virausgesot) 13,20 ± 0,70 sauerem Tempo: 25 ° CR an Identifizéierer Canonical Laachen O (CCOC) [C @
  • C13h19n5o5 ANONOsine, 2 '-o- (2-Methohyethyl) - (9ci, Aci)

    C13h19n5o5 ANONOsine, 2 '-o- (2-Methohyethyl) - (9ci, Aci)

    Storage Detail Cas Registry Nummer 168427-74 Tasteier-physesch Propriétraschendeswäerter Bedeelegungskondituladege Gewiicht 360,70 Ümt: 20 ° Preparéiert) Press: 760 Torr pka (virausgesot) 13.12 ± 0,70 sauer Tempo Tempo: 25 ° CR an Identifizéierer Canonical Laachen O (CCOC) [C @ h] 1 [C @@@ H] (O [
  • C21h21n36.66. Thymidine, α - [1-Naphthletylmemylyl) Amino.

    C21h21n36.66. Thymidine, α - [1-Naphthletylmemylyl) Amino.

    Stoff Detail Cas Registry Nummer 1262015-90-6 Schlëssel kierperlech Eegeschafte Wäerter Condulator Condular Gewiicht 411,41 - DENSPLED) Press: 760 Torr pka (virausgesot) C4OC (CO) c (o) c4 ° Laachen an £ NCC2 = CC = CC = 3C = CC = CC32) C4OC (CO) c (O) C4 Nimm an Identifizéierer laachen O = C2N (C = C (CCC = 2C3 = C (C = CC2) C = CC = C3) ...
  • C17h19n3o6 Thymidin, α -oxo- α - [Phhylnelthyl) Aminoer)

    C17h19n3o6 Thymidin, α -oxo- α - [Phhylnelthyl) Aminoer)

    Stoff Detail Cas Registry Nummer 944268-75-1 Schlëssel Physikalesch Propriéitéitswäerter Condular Condular Gewiicht 345,45 - Press: 760 Torr pka (virausgesot) 8,27 ± 0,10 Tomerik smile O = c1n ([C @@ H] 2o [c h] (co) [c@ h] (o) c2) c3) 1s / c17h19n3o6 / c21-9-13-12 (22) 6-14 (26-13) 20-8-11 (16) 19-17 (...
  • C9h11Fn2o5 uridine, 2 '' - 2 ''fluoro- (7ci, 8ci, 9ci, Hekti)

    C9h11Fn2o5 uridine, 2 '' - 2 ''fluoro- (7ci, 8ci, 9ci, Hekti)

    Stoff Detailsregistry Nummer 7841-4 H228 Key kierperlech Eegeschafte Wäerter morpular Versuch 256 - Mürmeleget) 149-150 ° Punkt 149-150 ide Dréckt: 760 Torr pka (virausgesot) 9.39 ± 0,10 Tempo Tempo Tempo: 25 ° CNOMMen, C2DIs £ C2C = C2C; C2C F [C @ h] 1 [C @@) 4 (3-13) (CO) [C @ H2) N2C (1 ... NC (CC (C2 INDE (C2HIMI INSIGN2O5 / C10-6- (15) 4 (C @ H] (CO) [C @
  • C10h12n2o5 6h-Furo [2 ', 3': 4.5] Oxazolo [3.2 - A] pyrimidin-6-Een, 9,3A-3--3 -7h12N12N2N2OL-

    C10h12n2o5 6h-Furo [2 ', 3': 4.5] Oxazolo [3.2 - A] pyrimidin-6-Een, 9,3A-3--3 -7h12N12N2N2OL-

    Stoff Detail Cas Registry Nummer 22423-26-3 Schlëssel kierperlech Eegeschafte Wäerter Bedeelegung morkular Gewiicht 240.21 - Schmelzpunkt (experimentell) 218 ​​° Punkt (Experiment Isopropanol Kachendepunkte (virausgesot) 460.0 ± 5-5 ° ° ° ° ° ° ° ° ° TRESS: 760 Torrdent) Press: 760 Torr pka (virausgesot) 12.56 ± 0,60 Tempo 2] 2 ([c @] (ncificene Laachen O = C2OC (C1N = C2OC (C1N = C2OC (C2OC (C1N:
  • C9h10n2o5 6H-Furo [2 ', 3': 4.5] - (9,2-A] ACIDin)

    C9h10n2o5 6H-Furo [2 ', 3': 4.5] - (9,2-A] ACIDin)

    Storage Detail Cas Registry Nummer 3736-77-4 Preparéiert) 2.101 ± 0,1 G / CM3 TOPTLESS) 256 (experimentent) 256 Press: 760 Torr pka (virausgesot) 12.55 ± 0,40 Tempo Tempo ([C @] (N3C (O2) NC (= O) C = C3) (O [C @@@ H] 1co) [H]) [H]