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线性分子式:
(C6H5)2PCH2P(C6H5)2
化学文摘社编号:
分子量:
384.39
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352002
EC Number:
218-194-2
MDL number:
Beilstein/REAXYS Number:
758760
产品名称
双(二苯基膦)甲烷, 97%
InChI key
XGCDBGRZEKYHNV-UHFFFAOYSA-N
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
SMILES string
C(P(c1ccccc1)c2ccccc2)P(c3ccccc3)c4ccccc4
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
Quality Level
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存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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The reactions between silver salts and borohydrides produce a rich set of products that range from discrete mononuclear compounds through to silver nanoparticles and colloids. Previous studies using electrospray ionization mass spectrometry (ESI-MS) to track the cationic products in solutions
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To determine whether neutropenia is associated with increased risk for infection in patients with systemic juvenile idiopathic arthritis (sJIA) and polyarticular-course juvenile idiopathic arthritis (pcJIA) treated with tocilizumab (TCZ). Data up to Week 104 from 2 phase III trials of
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)
Somayeh Behrouz et al.
Molecular diversity, 23(1), 147-164 (2018-08-11)
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
Walinka van Tol et al.
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
相关内容
Phosphine Ligand Application Guide
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