Tris[N,N,N,N-tetramethylguanidinium][tris(1S)-(1,1-binaphalene)-2,2-diolato]ytterbate Yb-HTMG-B

Catalog Number	ACM1611526750-1
CAS	1611526-75-0
Synonyms	hydron;1-(2-oxidonaphthalen-1-yl)naphthalen-2-olate;1,1,3,3-tetramethylguanidine;ytterbium(3+)
Molecular Weight	1374.52
Molecular Formula	C75H78N9O6Yb
Canonical SMILES	[H+].[H+].[H+].CN(C)C(=N)N(C)C.CN(C)C(=N)N(C)C.CN(C)C(=N)N(C)C.C1=CC=C2C(=C1)C=CC(=C2C3=C(C=CC4=CC=CC=C43)[O-])[O-].C1=CC=C2C(=C1)C=CC(=C2C3=C(C=CC4=CC=CC=C43)[O-])[O-].C1=CC=C2C(=C1)C=CC(=C2C3=C(C=CC4=CC=CC=C43)[O-])[O-].[Yb+3]
InChI	1S/3C20H14O2.3C5H13N3.Yb/c3*21-17-11-9-13-5-1-3-7-15(13)19(17)20-16-8-4-2-6-14(16)10-12-18(20)22;3*1-7(2)5(6)8(3)4;/h3*1-12,21-22H;3*6H,1-4H3;/q;+3/p-3
InChI Key	MMHOZKMKNPDMKI-UHFFFAOYSA-K
Purity	97%
Appearance	Off-white to pale yellow powder
Application	Catalyst used for an asymmetric Michael addition. Catalyst used for an asymmetric Michael addition of 1,3-dicarbonyls to enones. Catalyst used for the asymmetric aza-Michael addition of methylhydroxylamine to chalcone derivatives. Catalyst used for the asymmetric direct aldol reaction of acetophenone and pivaldehyde.
Complexity	1290
Covalently-Bonded Unit Count	10
Defined Atom Stereocenter Count	0
Exact Mass	1374.5463738
Heavy Atom Count	91
Hydrogen Bond Acceptor Count	9
Hydrogen Bond Donor Count	6
Monoisotopic Mass	1374.5463738
Rotatable Bond Count	6
Topological Polar Surface Area	229 Ų