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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Phosphorodichloridic acid, 2-chlorophenyl ester

Clc1ccccc1OP(=O)(Cl)Cl Request for Quotation
Chemical Name: Phosphorodichloridic acid, 2-chlorophenyl ester
CAS Number: 15074-54-1
Product Number: AG001MUK(AGN-PC-0JLVAM)
Synonyms:
MDL No:
Molecular Formula: C6H4Cl3O2P
Molecular Weight: 245.4275

Identification/Properties

Properties
BP:
270.5 °C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
245.42g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
243.901g/mol
Monoisotopic Mass:
243.901g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
193
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
3265
Hazard Statements:
H314
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
8
Packing Group:
Ⅱ

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Chlorophenyl phosphorodichloridate is a versatile chemical reagent commonly used in organic synthesis as a phosphorylating agent. It is primarily employed in the modification of biomolecules and small organic molecules to introduce phosphorus-containing functional groups. In chemical synthesis, this compound serves as a key intermediate for the preparation of various phosphorus-based compounds, such as phosphoramidates, phosphonates, and phosphates. Its ability to transfer phosphoryl groups makes it a valuable tool in the synthesis of nucleotide derivatives, phospholipids, and other phosphorus-containing organic compounds. Additionally, 2-Chlorophenyl phosphorodichloridate is widely utilized in the production of pharmaceuticals, agrochemicals, and materials science due to its reactivity and specific phosphorus chemistry.