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关于此项目
线性分子式:
C6H5NHP(O)(Cl)OC6H5
化学文摘社编号:
分子量:
267.65
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352002
EC Number:
257-400-5
MDL number:
InChI key
ZUQYQPGYEFBITH-UHFFFAOYSA-N
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)
SMILES string
ClP(=O)(Nc1ccccc1)Oc2ccccc2
assay
≥99%
form
solid
reaction suitability
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.)
Application
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
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Inhibition of chymotrypsin by phenyl N-phenyl-phosphoramidochloridate.
J Parkin et al.
Biochemical Society transactions, 20(3), 283S-283S (1992-08-01)
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