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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-trichloro-2-(chloromethoxy)-

ClCOCC(Cl)(Cl)Cl Request for Quotation
Chemical Name: Ethane, 1,1,1-trichloro-2-(chloromethoxy)-
CAS Number: 69573-75-7
Product Number: AG003OU0(AGN-PC-0NEJO1)
Synonyms:
MDL No:
Molecular Formula: C3H4Cl4O
Molecular Weight: 197.87526

Identification/Properties

Properties
Storage:
-10 ℃;
Form:
Liquid

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
2922
Hazard Statements:
H301+H311+H331-H314-H227
Precautionary Statements:
P501-P261-P270-P210-P271-P264-P280-P370+P378-P361+P364-P303+P361+P353-P301+P330+P331-P301+P310+P330-P304+P340+P310-P305+P351+P338+P310-P403+P233-P403+P235-P405
Class:
8,6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


Chloromethyl 2,2,2-Trichloroethyl Ether is a versatile compound commonly used in chemical synthesis as a chlorinating agent and a protecting group in organic reactions. In the synthesis of complex molecules, this reagent serves as a valuable tool for selectively introducing chlorine atoms into specific positions of organic substrates. Its high reactivity and ability to form stable intermediates make it a preferred choice for efficient transformations in the production of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, Chloromethyl 2,2,2-Trichloroethyl Ether plays a crucial role in protecting sensitive functional groups during various synthetic procedures, enabling precise control over regioselectivity and preventing unwanted side reactions. Its utility in strategic bond-forming processes highlights its significance in modern organic synthesis and its contribution to the advancement of chemical research and development.