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(R)-(-)-1,1'-Binaphthyl-2,2'-diyl Hydrogen Phosphate Asymmetric hetero Diels-Alder reaction catalyzed by chiral lanthanide(III) complex. Highly efficient Mannich reaction. Acidic Resolving agent for certain amine/racemic mixtures. Group: Chiral catalystschiral oxazaborolidines. Alternative Names: (R)-(-)-1,1'-BINAPHTHALENE-2,2'-DIYL-PHOSPHATE; 4-Hydroxydinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine 4-oxide; (R)-5,5 inverted exclamation mark ,6,6 inverted exclamation mark ,7,7 inverted exclamation mark ,8,8 inverted exclamation mark -Octahydro-1,1 inverted exclamation mark -binaphthyl-2,2 inverted exclamation mark -diyl hydrogen phosphate; -Binaphthyl-2,2; dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-ol 4-oxide; NSC244999; FT-0605235; (+)-4-Hydroxydinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin 4-oxide; O732; SC-04178. CAS No. 39648-67-4. Molecular formula: C20H13O4P. Mole weight: 348.294g/mol. IUPACName: 13-hydroxy-12, 14-dioxa-13λ5-phosphapentacyclo[13.8.0.02, 11.03, 8.018, 23]tricosa-1(15), 2(11), 3, 5, 7, 9, 16, 18, 20, 22-decaene 13-oxide. Canonical SMILES: C1=CC=C2C (=C1)C=CC3=C2C4=C (C=CC5=CC=CC=C54)OP (=O) (O3)O. ECNumber: 609-734-1. Catalog: ACM39648674. Alfa Chemistry. 2
(S)-(+)-1,1'-Binaphthyl-2,2'-diyl Hydrogen Phosphate Asymmetric hetero Diels-Alder reaction catalyzed by chiral lanthanide(III) complex. Highly efficient Mannich reaction Acidic Resolving agent for certain amine/racemic mixtures. Group: Chiral catalystschiral oxazaborolidines. Alternative Names: (aS)-2,2'-Phosphinicobisoxy-1,1'-binaphthalene; (R)-(-)-BNP ACID; AK163708; ANW-28102; SC11524; J-019988; (+/-)1,1'-binaphthyl-2,2'-diyl hydrogen phosphate; RT-003435; VC30236; (+/-)-2,2'-Dihydroxy-1,1'-binaphthyl Hydrogenphosphate. CAS No. 35193-64-7. Molecular formula: C20H13O4P. Mole weight: 348.294g/mol. IUPACName: 13-hydroxy-12, 14-dioxa-13λ5-phosphapentacyclo[13.8.0.02, 11.03, 8.018, 23]tricosa-1(15), 2(11), 3, 5, 7, 9, 16, 18, 20, 22-decaene 13-oxide. Canonical SMILES: C1=CC=C2C (=C1)C=CC3=C2C4=C (C=CC5=CC=CC=C54)OP (=O) (O3)O. ECNumber: 609-734-1. Catalog: ACM35193647. Alfa Chemistry. 2
(S)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine Convenient catalyst for the enantioselective borane reduction of ketones at ambient temperatures. Asymmetric synthesis of α-chiral hydroxyalkylphosphines via a catalytic, enantioselective reduction of acylphosphines. Nickel-catalyzed cross-couplings of benzylic pivalates with arylboroxines: Stereospecific formation of diarylalkanes and triarylmethanes. Enantioselective reduction of prochiral ketones with NaBH4/Me2SO4/(S)-Me-CBS. Group: Other. Alternative Names: AKOS015840981; (S)-1-methyl-3,3-diphenyltetrahydro-1H,3H-pyrrolo[1,2-c][1,3,2]oxazaborole; MFCD00078439; (S)- Methyl-CBS-oxazaborolidine; ZINC169743318; (S)-tetrahydro-1-methyl-3,3-diphenyl-1 H,3 H-pyrrolo[1,2-c][1,3,2] oxazaborole; (S)-1-methyl-3,3-diphenylhexahydropyrrolo-[1,2-c][1,3,2]oxazaborole; (S)-tetrahydro-1-methyl-3,3-diphenyl-1 H,3H-pyrrolo[1,2-c]-[1,3,2]oxazaborole; (S)-Me-CBS; Corey catalyst. CAS No. 112022-81-8. Molecular formula: C18H20BNO. Mole weight: 277.174g/mol. IUPACName: (3aS)-1-methyl-3,3-diphenyl-3a,4,5,6-tetrahydropyrrolo[1,2-c][1,3,2]oxazaborole. Canonical SMILES: B1 (N2CCCC2C (O1) (C3=CC=CC=C3)C4=CC=CC=C4)C. Catalog: ACM112022818. Alfa Chemistry. 2
(S)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine (S)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine. Uses: Convenient catalyst for the enantioselective borane reduction of ketones at ambient temperatures. asymmetric synthesis of α-chiral hydroxyalkylphosphines via a catalytic, enantioselective reduction of acylphosphines. nickel-catalyzed cross-couplings of benzylic pivalates with arylboroxines: stereospecific formation of diarylalkanes and triarylmethanes. enantioselective reduction of prochiral ketones with nabh4/me2so4/(s)-me-cbs. Group: other electronic materials. Alternative Names: AKOS015840981; (S)-1-methyl-3,3-diphenyltetrahydro-1H,3H-pyrrolo[1,2-c][1,3,2]oxazaborole; MFCD00078439; (S)- Methyl-CBS-oxazaborolidine; ZINC169743318; (S)-tetrahydro-1-methyl-3,3-diphenyl-1 H,3 H-pyrrolo[1,2-c][1,3,2] oxazaborole; (S)-1-methyl-3,3-diphenylhexahydropyrrolo-[1,2-c][1,3,2]oxazaborole; (S)-tetrahydro-1-methyl-3,3-diphenyl-1 H,3H-pyrrolo[1,2-c]-[1,3,2]oxazaborole; (S)-Me-CBS; Corey catalyst. CAS No. 112022-81-8. Product ID: (3aS)-1-methyl-3,3-diphenyl-3a,4,5,6-tetrahydropyrrolo[1,2-c][1,3,2]oxazaborole. Molecular formula: 277.174g/mol. Mole weight: C18H20BNO. B1 (N2CCCC2C (O1) (C3=CC=CC=C3)C4=CC=CC=C4)C. InChI=1S / C18H20BNO / c1-19-20-14-8-13-17 (20) 18 (21-19, 15-9-4-2-5-10-15) 16-11-6-3-7-12-16 / h2-7, 9-12, 17H, 8, 13-14H2, 1H3 / t17- / m0 / s1. VMKAFJQFKBASMU-KRWDZBQOSA-N. Alfa Chemistry Materials 3

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