Name: Name:Phenyl Phosphorodichloridate
Brand: AABLOCKS
SKU: AA0035E8
Rating: 90 (10 reviews)

Catalog No.: AA0035E8

770-12-7 | Phenyl Phosphorodichloridate

Pack Size： 10g

Purity： 95%

in stock

$18.00 $13.00

Pack Size： 25g

Purity： 95%

in stock

$24.00 $17.00

Pack Size： 500g

Purity： >98.0%(T)

in stock

$343.00 $240.00

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Technical Information

Catalog Number: AA0035E8

Chemical Name: Phenyl Phosphorodichloridate

CAS Number: 770-12-7

Molecular Formula: C6H5Cl2O2P

Molecular Weight: 210.9825

MDL Number: MFCD00002067

SMILES: ClP(=O)(Oc1ccccc1)Cl

NSC Number: 44412

UN Number: 3265

Properties

BP: 242.0°C

Form: Liquid

MP: -1 °C

Refractive Index: n20/D 1.523(lit.)

Stability: Moisture Sensitive

Storage: 2-8℃;

Complexity: 162

Covalently-Bonded Unit Count: 1

Defined Atom Stereocenter Count: 0

Defined Bond Stereocenter Count: 0

Formal Charge: 0

Heavy Atom Count: 11

Hydrogen Bond Acceptor Count: 2

Hydrogen Bond Donor Count: 0

Isotope Atom Count: 0

Rotatable Bond Count: 2

Undefined Atom Stereocenter Count: 0

Undefined Bond Stereocenter Count: 0

XLogP3: 2.8

Literature fold

Title: Phenyl bis-(m-tolyl-amido)-phosphinate.

Journal: Acta crystallographica. Section E, Structure reports online20110801

Title: Phenyl bis-(morpholin-4-yl-amido)-phosphinate.

Journal: Acta crystallographica. Section E, Structure reports online20110801

Title: 3-(6-Methyl-2-pyrid-yl)-2-phen-oxy-3,4-dihydro-1,3,2-benzoxaza-phosphirine 2-oxide.

Journal: Acta crystallographica. Section E, Structure reports online20090801

Title: Synthesis and biological evaluation of phosphate prodrugs of 4-phospho-D-erythronohydroxamic acid, an inhibitor of 6-phosphogluconate dehydrogenase.

Journal: ChemMedChem20070813

Title: Efficient and chemoselective N-acylation of 10-amino-7-ethyl camptothecin with poly(ethylene glycol).

Journal: Bioorganic & medicinal chemistry letters20040405

Title: Selective phenolic acylation of 10-hydroxycamptothecin using poly (ethylene glycol) carboxylic acid.

Journal: Bioorganic & medicinal chemistry letters20030210

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