Not AvailableNot AvailableNot Available
Common NameCo-precorrin-5b
DescriptionNot Available
Structure
Molecular FormulaC43H42CoN4O16
Average Mass929.75900
Monoisotopic Mass929.19716
IUPAC NameNot Available
Traditional NameNot Available
CAS Registry NumberNot Available
SMILESC[C@]1(CC(=O)[O-])C(CCC(=O)[O-])=C2C[C@@]3(C)C(CC(=O)[O-])=C(CCC(=O)[O-])C4=CC5=[N+]6C(=C7N8C(=CC1=[N+]2[Co-2]86N43)[C@@H](CCC(=O)[O-])[C@]7(C)CC(=O)[O-])[C@H](CC(=O)[O-])[C@@]5(C)CCC(=O)[O-]
InChI IdentifierInChI=1S/C43H52N4O16.Co/c1-40(12-11-33(54)55)24(14-35(58)59)38-39-42(3,19-37(62)63)21(6-9-31(50)51)26(45-39)16-29-41(2,18-36(60)61)22(7-10-32(52)53)27(44-29)17-43(4)23(13-34(56)57)20(5-8-30(48)49)25(47-43)15-28(40)46-38;/h15-16,21,24H,5-14,17-19H2,1-4H3,(H10,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63);/q;+2/p-10/b39-38+;/t21-,24+,40-,41+,42+,43+;/m1./s1
InChI KeyXHLLHKIBBMZXKO-AQTLHMIISA-D
CHEBI IDCHEBI:60063
MiMeDB IDMMDBc0055816
StateExpected Solid
Water SolubilityNot Available
logSNot Available
pKa (Strongest Acidic)Not Available
pKa (Strongest Basic)Not Available
Hydrogen Acceptor CountNot Available
Hydrogen Donor CountNot Available
Rotatable Bond CountNot Available
Physiological ChargeNot Available
Formal ChargeNot Available
PolarizabilityNot Available

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