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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)-

Ethane, 1,1',1''-[methylidynetris(oxy)]tris[2-chloro-

ClCCC(C([O-])([O-])[O-])(CCCl)CCl Request for Quotation
Chemical Name: Ethane, 1,1',1''-[methylidynetris(oxy)]tris[2-chloro-
CAS Number: 18719-58-9
Product Number: AG003V71(AGN-PC-0JLX0A)
Synonyms:
MDL No:
Molecular Formula: C7H10Cl3O3---
Molecular Weight: 248.5115

Identification/Properties

Properties
BP:
293.1℃
Storage:
Room Temperature;
Computed Properties
Molecular Weight:
251.528g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
9
Exact Mass:
249.993g/mol
Monoisotopic Mass:
249.993g/mol
Topological Polar Surface Area:
27.7A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
86
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Tris(2-chloroethyl)-orthoformate, commonly known as TCEF, is a versatile chemical compound widely used in various chemical synthesis applications. With its unique properties, TCEF serves as an essential reagent in organic chemistry for the efficient and selective functionalization of molecules. In chemical synthesis, TCEF is commonly employed as a reagent for the introduction of the chloroethyl group into organic compounds, facilitating the synthesis of a diverse range of valuable products. This reagent is particularly useful in reactions involving nucleophilic substitution, where the chloroethyl group acts as a leaving group, enabling the formation of new carbon-carbon and carbon-heteroatom bonds. Furthermore, TCEF is prized for its stability and compatibility with a wide range of functional groups, making it a preferred choice for chemists seeking to modify complex molecules with precision and control. Its ease of handling and high reactivity make it a valuable tool in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Overall, the application of Tris(2-chloroethyl)-orthoformate in chemical synthesis offers chemists a powerful and reliable method for introducing chloroethyl functionality into organic molecules, opening up new possibilities for the development of novel compounds and materials.