sSPhos Pd G2

95%

Reagent Code: #237427
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CAS Number 2375242-78-5

science Other reagents with same CAS 2375242-78-5

blur_circular Chemical Specifications

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Weight 822.66 g/mol
Formula C₃₈H₄₄ClNNaO₅PPdS
badge Registry Numbers
MDL Number MFCD22377809
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, inert gas

description Product Description

Used as a highly active palladium-based catalyst in cross-coupling reactions, particularly in Suzuki-Miyaura couplings. It enables efficient carbon-carbon bond formation under mild conditions, often with low catalyst loading. Effective for coupling aryl chlorides, which are less reactive and more cost-effective than bromides or iodides, making it valuable in pharmaceutical and agrochemical synthesis. Tolerant of a wide range of functional groups, allowing use in complex molecule assembly. Commonly applied in late-stage functionalization where high selectivity and minimal side reactions are critical.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,870.00
inventory 500mg
10-20 days ฿42,810.00

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sSPhos Pd G2
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Used as a highly active palladium-based catalyst in cross-coupling reactions, particularly in Suzuki-Miyaura couplings. It enables efficient carbon-carbon bond formation under mild conditions, often with low catalyst loading. Effective for coupling aryl chlorides, which are less reactive and more cost-effective than bromides or iodides, making it valuable in pharmaceutical and agrochemical synthesis. Tolerant of a wide range of functional groups, allowing use in complex molecule assembly. Commonly applie

Used as a highly active palladium-based catalyst in cross-coupling reactions, particularly in Suzuki-Miyaura couplings. It enables efficient carbon-carbon bond formation under mild conditions, often with low catalyst loading. Effective for coupling aryl chlorides, which are less reactive and more cost-effective than bromides or iodides, making it valuable in pharmaceutical and agrochemical synthesis. Tolerant of a wide range of functional groups, allowing use in complex molecule assembly. Commonly applied in late-stage functionalization where high selectivity and minimal side reactions are critical.

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