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Merck

190780

Sodium trichloroacetate

97%

Sinónimos:

NaTCA, TCA sodium salt, Trichloroacetic acid sodium salt

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About This Item

Fórmula lineal:
CCl3CO2Na
Número CAS:
Peso molecular:
185.37
UNSPSC Code:
12352302
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-479-2
Beilstein/REAXYS Number:
3773249
MDL number:
assay:
97%

Nombre del producto

Sodium trichloroacetate, 97%

InChI key

SAQSTQBVENFSKT-UHFFFAOYSA-M

InChI

1S/C2HCl3O2.Na/c3-2(4,5)1(6)7;/h(H,6,7);/q;+1/p-1

SMILES string

[Na+].[O-]C(=O)C(Cl)(Cl)Cl

assay

97%

functional group

chloro

Quality Level

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Application

Sodium trichloroacetate with trichloroacetic acid (TCA) undergoes rapid decarboxylation in dimethylformamide (DMF) in the presence of aldehydes to form nucleophilic trichloromethyl anion, which then adds to the aldehydes to form trichloromethyl carbinols. It can also undergo thermal decarboxylation in aprotonic solvents in the presence of olefins to generate dichlorocarbene as an intermediate.

pictograms

Exclamation markEnvironment

signalword

Warning

hcodes

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - STOT SE 3

target_organs

Respiratory system

Clase de almacenamiento

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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The thermal decarboxylation of alkali trichloroacetates in aprotic solvents. II. Decarboxylation in the presence of olefins.
Wagner WM
Rec. Trav. Chim., 80(7), 740-746 (1961)
Two effective procedures for the synthesis of trichloromethyl ketones, useful precursors of chiral ?-amino and ?-hydroxy acids.
Corey EJ
Tetrahedron Letters, 33(24), 3435-3438 (1992)
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