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224308

Sigma-Aldrich

Dilithium tetrachlorocuprate(II) solution

0.1 M in THF

Synonym(s):

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

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About This Item

Linear Formula:
Li2CuCl4
CAS Number:
15489-27-7
Molecular Weight:
219.24
EC Number:
203-726-8
MDL number:
MFCD00011081
UNSPSC Code:
12352302
PubChem Substance ID:
24853427
NACRES:
NA.23

form

liquid

reaction suitability

reagent type: catalyst
core: copper

concentration

0.1 M in THF

density

0.91 g/mL at 25 °C

SMILES string

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

InChI

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

InChI key

HCJWWBBBSCXJMS-UHFFFAOYSA-J

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Application

Catalyst used to couple alkyl halides with alkyl Grignard reagents.

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

EUH019

Storage Class

3 - Flammable liquids

wgk_germany

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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Certificates of Analysis (COA)

Lot/Batch Number
MKCM6669
SHBH5044V
SHBF1928V
SHBD5688V
SHBB7589V

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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)
Tetrahedron, 62, 4851-4851 (2006)
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:

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