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Merck

127566

Sigma-Aldrich

Bis(diphenylphosphino)methane

97%

Sinónimos:

DPPM, Methanediylbis[diphenylphosphine, Tetraphenylmethylenediphosphine, DPM, Methylenebis(diphenylphosphine)

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About This Item

Fórmula lineal:
(C6H5)2PCH2P(C6H5)2
Número de CAS:
Peso molecular:
384.39
Beilstein/REAXYS Number:
758760
EC Number:
MDL number:
UNSPSC Code:
12352002
PubChem Substance ID:
NACRES:
NA.22

assay

97%

form

solid

reaction suitability

reagent type: ligand
reaction type: Heck Reaction

reagent type: ligand
reaction type: Suzuki-Miyaura Coupling

mp

118-119 °C (lit.)

functional group

phosphine

SMILES string

C(P(c1ccccc1)c2ccccc2)P(c3ccccc3)c4ccccc4

InChI

1S/C25H22P2/c1-5-13-22(14-6-1)26(23-15-7-2-8-16-23)21-27(24-17-9-3-10-18-24)25-19-11-4-12-20-25/h1-20H,21H2

InChI key

XGCDBGRZEKYHNV-UHFFFAOYSA-N

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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The design, synthesis, antinociceptive and β-adrenoceptor blocking activities of several eugenyloxy propanol azole derivatives have been described. In this synthesis, the reaction of eugenol with epichlorohydrin provided adducts 3 and 4 which were N-alkylated by diverse azoles to obtain the
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Journal of inherited metabolic disease, 42(5), 984-992 (2019-04-02)
The congenital disorders of glycosylation (CDG) are inborn errors of metabolism with a great genetic heterogeneity. Most CDG are caused by defects in the N-glycan biosynthesis, leading to multisystem phenotypes. However, the occurrence of tissue-restricted clinical symptoms in the various
Robert R A Freund et al.
Dalton transactions (Cambridge, England : 2003), 43(37), 13988-14000 (2014-08-15)
A series of allyl modified nickelalactone derivatives of the general formula [(L)nNi{CH2C(CH3)C(CH3)CH2COO}] was synthesized via ligand exchange reactions in order to investigate the influence of the neutral ligand L on the structure and stability of these complexes. While the square
Jun-Ichi Wachino et al.
mBio, 11(2) (2020-03-19)
Production of metallo-β-lactamases (MBLs), which hydrolyze carbapenems, is a cause of carbapenem resistance in Enterobacteriaceae Development of effective inhibitors for MBLs is one approach to restore carbapenem efficacy in carbapenem-resistant Enterobacteriaceae (CRE). We report here that sulfamoyl heteroarylcarboxylic acids (SHCs)

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