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化驗
≥99%
形狀
solid
反應適用性
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
mp
132-134 °C (lit.)
SMILES 字串
ClP(=O)(Nc1ccccc1)Oc2ccccc2
InChI
1S/C12H11ClNO2P/c13-17(15,14-11-7-3-1-4-8-11)16-12-9-5-2-6-10-12/h1-10H,(H,14,15)
InChI 密鑰
ZUQYQPGYEFBITH-UHFFFAOYSA-N
應用
Reactant for synthesis of:
Reactant for:
Catalyst for polymerization reactions
Involved in biological studies for chymotrypsin binding and inhibition
- Resin-immobilized actinide ligands
- Carboxylic acid anhydrides and their derivatives
- Thiadiaminooxopyrimidine derivatives for antitumor activity
- Polyanhydrides via dehydrative coupling agents
Reactant for:
- One-pot conversion of pyrimidinones to pyrimidines
- Conversion to alkyl Ph diester
Catalyst for polymerization reactions
Involved in biological studies for chymotrypsin binding and inhibition
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
Inhibition of chymotrypsin by phenyl N-phenyl-phosphoramidochloridate.
Biochemical Society transactions, 20(3), 283S-283S (1992-08-01)
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