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224308

Dilithium tetrachlorocuprate(II) solution

0.1 M in THF

Synonym(s):

Copper dilithium tetrachloride, Dilithium tetrachlorocuprate(2-), Lithium Tetrachlorocuprate

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800 ML

$288.00

100 ML

$382.00

$288.00


Estimated to ship onJanuary 12, 2026Details

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About This Item

Linear Formula:
Li2CuCl4
CAS Number:
Molecular Weight:
219.24
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
203-726-8
MDL number:
Form:
liquid

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Product Name

Dilithium tetrachlorocuprate(II) solution, 0.1 M in THF

InChI key

HCJWWBBBSCXJMS-UHFFFAOYSA-J

InChI

1S/4ClH.Cu.2Li/h4*1H;;;/q;;;;+2;2*+1/p-4

SMILES string

[Li+].[Li+].Cl[Cu--](Cl)(Cl)Cl

form

liquid

reaction suitability

reagent type: catalyst

concentration

0.1 M in THF

density

0.91 g/mL at 25 °C

application(s)

battery precursors
catalysts
material synthesis precursor

Quality Level

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1 of 4

This Item
697257398195703524
form

liquid

form

liquid

form

liquid

form

liquid

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

density

0.91 g/mL at 25 °C

density

0.999 g/mL at 25 °C

density

0.888 g/mL at 25 °C

density

0.73 g/mL at 25 °C

reaction suitability

reagent type: catalyst
core: copper

reaction suitability

-

reaction suitability

-

reaction suitability

-

concentration

0.1 M in THF

concentration

in anhydrous tetrahydrofuran

concentration

1.0 M in THF

concentration

40 % (w/w) in heptanes, ~3.1 M in heptane

Application

Catalyst used to couple alkyl halides with alkyl Grignard reagents.[1]

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3

target_organs

Respiratory system

supp_hazards

Storage Class

3 - Flammable liquids

wgk

WGK 2

flash_point_f

1.4 °F - closed cup

flash_point_c

-17 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Kenji Mori
Bioscience, biotechnology, and biochemistry, 74(3), 595-600 (2010-03-09)
A mixture of the four stereoisomers of 1,7-dimethylnonyl propanoate, the female sex pheromone of the western corn rootworm (Diabrotica virgifera virgifera LeConte), was synthesized in four different ways by employing one of the following four reactions as the key step:
Tetrahedron, 62, 4851-4851 (2006)
K Minamoto et al.
Nucleic acids symposium series, (27)(27), 109-110 (1992-01-01)
The reaction of 1-(2,3-anhydro-5-O-trityl-beta-D-lyxofuranosyl)-2-O-methyluracil (1a) and its thymine analogue (1b) with dilithium tetrahalocuprate (Li2CuX4) revealed excellent to perfect regioselectivity, yielding 2,2'-anhydro-3'-halonucleosides (2a-d), while the same reactions with 2,3-anhydro uracil and thymine nucleosides (4a,b) gave arabinosyl (5a-d) and xylosyl halohydrins (6a-d)

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