Home Halogens Diphenyl chlorophosphate

Diphenyl chlorophosphate

CAS No.:
2524-64-3
Catalog Number:
AG0034S0
Molecular Formula:
C12H10ClO3P
Molecular Weight:
268.6328
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
98%
In Stock USA
United States
$13
- +
30g
98%(GC)
In Stock USA
United States
$58
- +
Product Description
Catalog Number:
AG0034S0
Chemical Name:
Diphenyl chlorophosphate
CAS Number:
2524-64-3
Molecular Formula:
C12H10ClO3P
Molecular Weight:
268.6328
MDL Number:
MFCD00003030
IUPAC Name:
[chloro(phenoxy)phosphoryl]oxybenzene
InChI:
InChI=1S/C12H10ClO3P/c13-17(14,15-11-7-3-1-4-8-11)16-12-9-5-2-6-10-12/h1-10H
InChI Key:
BHIIGRBMZRSDRI-UHFFFAOYSA-N
SMILES:
ClP(=O)(Oc1ccccc1)Oc1ccccc1
EC Number:
219-759-6
UNII:
1KEE9757OT
NSC Number:
43771
UN Number:
1760
Properties
Complexity:
249  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
268.006g/mol
Formal Charge:
0
Heavy Atom Count:
17  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
268.633g/mol
Monoisotopic Mass:
268.006g/mol
Rotatable Bond Count:
4  
Topological Polar Surface Area:
35.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.5  
Literature
Title Journal
Reactive intermediates in the H-phosphonate synthesis of oligonucleotides. Organic & biomolecular chemistry 20120814
Aryl H-phosphonates 17: (N-aryl)phosphoramidates of pyrimidine nucleoside analogues and their synthesis, selected properties, and anti-HIV activity. Journal of medicinal chemistry 20111013
Carbon dioxide as a carbonylating agent in the synthesis of 2-oxazolidinones, 2-oxazinones, and cyclic ureas: scope and limitations. The Journal of organic chemistry 20100507
Diphenyl (benzyl-amido)phosphate. Acta crystallographica. Section E, Structure reports online 20100101
Efficient chemical synthesis of both anomers of ADP L-glycero- and D-glycero-D-manno-heptopyranose. Carbohydrate research 20031114
Synthesis of P(1)-Citronellyl-P(2)-alpha-D-pyranosyl pyrophosphates as potential substrates for the E. coli undecaprenyl-pyrophosphoryl-N-acetylglucoseaminyl transferase MurG. Bioorganic & medicinal chemistry letters 20011217
Properties