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Merck
CN

670693

(−)-2,3-Bis[(2R,5R)-2,5-dimethylphospholano]maleic anhydride

98%

Synonym(s):

3,4-Bis[(2R,5R)-2,5-dimethyl-1-phospholanyl]furan-2,5-dione, catASium® M(R)

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About This Item

Empirical Formula (Hill Notation):
C16H24O3P2
CAS Number:
Molecular Weight:
326.31
PubChem Substance ID:
UNSPSC Code:
12352005
Beilstein/REAXYS Number:
9428339
MDL number:
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SMILES string

C[C@@H]1CC[C@@H](C)P1C2=C(P3[C@H](C)CC[C@H]3C)C(=O)OC2=O

InChI

1S/C16H24O3P2/c1-9-5-6-10(2)20(9)13-14(16(18)19-15(13)17)21-11(3)7-8-12(21)4/h9-12H,5-8H2,1-4H3/t9-,10-,11-,12-/m1/s1

InChI key

OQHMFJKKVZGWDC-DDHJBXDOSA-N

assay

≥98% (31P-NMR), 98%

Quality Level

General description

Sold in collaboration with Solvias AG

Application

(−)-2,3-Bis[(2R,5R)-2,5-dimethylphospholano]maleic anhydride can be used to prepare its rhodium metal complexes, which are used as catalysts in the asymmetric hydrogenation reactions of alkenes.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Legal Information

catASium is a registered trademark of Umicore AG & Co. KG

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Activation, Deactivation and Reversibility Phenomena in Homogeneous Catalysis: A Showcase Based on the Chemistry of Rhodium/Phosphine Catalysts
Alberico E, et al.
Catalysts, 9(7), 582-582 (2019)
Asymmetric Synthesis of Potential Precursors of the HIV Drug MC1220 and Its Analogues by Hydrogenation of (1-Arylvinyl) pyrimidines
Loksha YM and Pedersen EB
Journal of Heterocyclic Chemistry, 55(6), 1352-1357 (2018)

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