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2524-64-3,MFCD00003030
Catalog No.:AA0034P8

2524-64-3 | Diphenyl chlorophosphate

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25g
>95.0%(GC)
in stock  
$22.00   $16.00
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500g
95%
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  • Technical Information
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA0034P8
Chemical Name:
Diphenyl chlorophosphate
CAS Number:
2524-64-3
Molecular Formula:
C12H10ClO3P
Molecular Weight:
268.6328
MDL Number:
MFCD00003030
SMILES:
ClP(=O)(Oc1ccccc1)Oc1ccccc1
NSC Number:
43771
UN Number:
1760
Properties
Properties
 
BP:
363.5°C at 760 mmHg  
Form:
Liquid  
Refractive Index:
n20/D 1.55(lit.)  
Stability:
Moisture Sensitive  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
249  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
17  
Hydrogen Bond Acceptor Count:
3  
Rotatable Bond Count:
4  
XLogP3:
3.5  

Literature

Title: Reactive intermediates in the H-phosphonate synthesis of oligonucleotides.

Journal: Organic & biomolecular chemistry 20120814

Title: Aryl H-phosphonates 17: (N-aryl)phosphoramidates of pyrimidine nucleoside analogues and their synthesis, selected properties, and anti-HIV activity.

Journal: Journal of medicinal chemistry 20111013

Title: Carbon dioxide as a carbonylating agent in the synthesis of 2-oxazolidinones, 2-oxazinones, and cyclic ureas: scope and limitations.

Journal: The Journal of organic chemistry 20100507

Title: Diphenyl (benzyl-amido)phosphate.

Journal: Acta crystallographica. Section E, Structure reports online 20100101

Title: Efficient chemical synthesis of both anomers of ADP L-glycero- and D-glycero-D-manno-heptopyranose.

Journal: Carbohydrate research 20031114

Title: Synthesis of P(1)-Citronellyl-P(2)-alpha-D-pyranosyl pyrophosphates as potential substrates for the E. coli undecaprenyl-pyrophosphoryl-N-acetylglucoseaminyl transferase MurG.

Journal: Bioorganic & medicinal chemistry letters 20011217

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