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665231

Sigma-Aldrich

(+)-1,2-Bis[(2R,5R)-2,5-dimethylphospholano]ethane

kanata purity

Synonym(s):

(R,R)-Me-BPE

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About This Item

Empirical Formula (Hill Notation):
C14H28P2
CAS Number:
129648-07-3
Molecular Weight:
258.32
MDL number:
MFCD01073770
UNSPSC Code:
12352005
PubChem Substance ID:
24884723
NACRES:
NA.22

refractive index

n20/D 1.534

bp

64-67 °C/0.06 mmHg

density

0.940 g/mL at 25 °C

SMILES string

C[C@@H]1CC[C@@H](C)P1CCP2[C@H](C)CC[C@H]2C

InChI

1S/C14H28P2/c1-11-5-6-12(2)15(11)9-10-16-13(3)7-8-14(16)4/h11-14H,5-10H2,1-4H3/t11-,12-,13-,14-/m1/s1

InChI key

IRCDUOCGSIGEAI-AAVRWANBSA-N

Application

DuPhos and BPE Ligands: Highly Efficient Privileged Ligands

Legal Information

Sold in collaboration with Kanata Chemical Technologies Inc. for research purposes only. These compounds were made and sold under license from E.I. du Pont de Nemours and Company, which license does not include the right to use the compounds in producing products for sale in the pharmaceutical field.

Pictograms

Flame
GHS02

Signal Word

Danger

Hazard Statements

H250,H413

Precautionary Statements

P222 - P231 - P422

Hazard Classifications

Aquatic Chronic 4 - Pyr. Liq. 1

Storage Class Code

4.2 - Pyrophoric and self-heating hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCF7600
MKBG8844V
15302BE

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Articles

DuPhos and BPE Ligands

Asymmetric hydrogenation enables scalable synthesis of single-enantiomer compounds with minimal byproducts, ideal for commercial manufacturing.

DuPhos and BPE Ligands

Asymmetric hydrogenation enables scalable synthesis of single-enantiomer compounds with minimal byproducts, ideal for commercial manufacturing.

DuPhos and BPE Ligands

Asymmetric hydrogenation enables scalable synthesis of single-enantiomer compounds with minimal byproducts, ideal for commercial manufacturing.

DuPhos and BPE Ligands

Asymmetric hydrogenation enables scalable synthesis of single-enantiomer compounds with minimal byproducts, ideal for commercial manufacturing.

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