Substance
ID:338741
Names and Identifiers
IUPAC Traditional name
phenoxy(phenylamino)phosphinoyl chloride
IUPAC name
phenoxy(phenylamino)phosphinoyl chloride
Synonyms
Phenyl N-phenylphosphoramidochloridateN-苯基磷氨基氯化苯N-Phenylphosphoramidochloridic acid phenyl ester
Properties
Safety Information
GHS Signal Word
Warning
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Risk Statements
36/37/38
European Hazard Symbols
Irritant (Xi)Safety Statements
26-36
GHS Precautionary statements
P261-P305+P351+P338
MSDS Link
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
German water hazard class
3
GHS Hazard statements
H315-H319-H335
Physical Property
Melting Point
132-134 °C(lit.)
Product Information
Linear Formula
C6H5NHP(O)(Cl)OC6H5
Purity
≥99%
Molecule Details
Packaging
5 g in glass bottle
Application
Reactant for synthesis of:
• Resin-immobilized actinide ligands1
• Carboxylic acid anhydrides and their derivatives2
• Thiadiaminooxopyrimidine derivatives for antitumor activity3
• Polyanhydrides via dehydrative coupling agents4Reactant for:
• One-pot conversion of pyrimidinones to pyrimidines5
• Conversion to alkyl Ph diester6Catalyst for polymerization reactions7Involved in biological studies for chymotrypsin binding and inhibition8
5 g in glass bottle
Application
Reactant for synthesis of:
• Resin-immobilized actinide ligands1
• Carboxylic acid anhydrides and their derivatives2
• Thiadiaminooxopyrimidine derivatives for antitumor activity3
• Polyanhydrides via dehydrative coupling agents4Reactant for:
• One-pot conversion of pyrimidinones to pyrimidines5
• Conversion to alkyl Ph diester6Catalyst for polymerization reactions7Involved in biological studies for chymotrypsin binding and inhibition8
Molecular Spectra
No Data Available
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References
No Data Available
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