CAS: | 739-58-2 | ||||
分子式: | C20H20NP | ||||
分子量: | 305.35 | ||||
熔点: | 151-154℃ | ||||
英文名称: |
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货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | 详情 | ||||||||||||||||||||||||||||||||||||||||||||||||||||
D822223 | MACKLIN | 4-(二甲氨基)三苯基膦 | 95.0%(GC) | 27元/250mg; 66元/5g; 320元/25g; 1068元/100g; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||||||
储存:室温 状态:灰白色固体 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
D2478 | TCI | 4-(Dimethylamino)phenyldiphenylphosphine | >95.0%(GC) | 250元/1G; 890元/5G; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||||||
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404193 | J&K | 4-(Dimethylamino)phenyldiphenylphosphine | 95% | 220元/1G; 726元/5G; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||||||
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15-1380 | Strem | Diphenyl[4-(N,N-dimethylamino)phenyl]phosphine | min. 95% | 556元/1g; 2168元/5g; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Technical Notes: 1.Reductive Amination: Catalyst for the organocatalytic asymmetric reductive amination of aldehydes. 2.Treating racemic a-branched aldehydes with p-anisidine and a Hantzsch ester in the presence of catalyst, TRIP, gave ß-branched secondary amines. 3.a-Allylation: Highly enantioselective Pd/chiral acid-catalyzed a-allylation of a-branched aldehydes with an allyl amine as the allylating species, that creates all-carbon quaternary stereogenic centers in high yields and enantioselectivities . 3.Hydrogenation: A achiral amine in combination with a catalytic amount of a chiral Brønsted acid can accomplish an aldol addition-dehydration-conjugate reduction-reductive amination to provide potential intermediates of pharmaceutically active compounds in good yields and excellent enantioselectivities. 4.Friedel-Crafts Reaction: The first enantioselective catalysis of the Friedel-Crafts reaction via activation of electron-rich multiple bonds by a chiral Brønsted acid. 5.Allylboration: A new high-yielding and highly enantioselective chiral Brønsted acid-catalyzed allylboration of aldehydes . 6.Aza-Darzens Reaction: Aza-Darzens reaction of ethyl diazoacetate with aldimines, derived from phenyl glyoxal, furnished cis-aziridine carboxylates with excellent enantioselectivities by means of a chiral phosphoric acid . 7. Intramolecular Aldol Condens ation: Transformation applicable to a wide variety of substrates to give chiral cyclohexenones in high yields and with excellent enantioselectivity | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
395021 | Sigma-Aldrich | 4-(Dimethylamino)phenyldiphenylphosphine | 95% | 1204.99元/5 G; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||||||
产品说明 应用 Catalyst for:
Reducing agent for selectivity of disulfide-internally linked peptide-nucleic acid cleavage 包装 5 g in glass bottle 基本信息
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047066 | Fluorochem | 4-(Dimethylamino)phenyldiphenyl phosphine | 96% | 220元/1g; 396元/5g; 748元/10g; 1804元/25g; 7150元/100g; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||||||
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