추천 제품
분석
≥99%
형태
solid
반응 적합성
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 string
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 key
ZUQYQPGYEFBITH-UHFFFAOYSA-N
애플리케이션
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
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
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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