ChemicalBook--->CAS DataBase List--->68986-76-5

68986-76-5

68986-76-5 Structure

68986-76-5 Structure
IdentificationBack Directory
[Name]

COPPER(I) THIOPHENE-2-CARBOXYLATE
[CAS]

68986-76-5
[Synonyms]

Thiophene-2-carbonyloxycopper
(2-Thiophenecarboxylato)copper
Cuprous 2-thiophenecarboxylate
Copper(I) thiophene-2-carboxyL
Copper (I) thiophenecarboxylate
Copper(I) 2-Thiophenecarboxylate
(2-Thiophenecarboxylato)copper(I)
Copper(1+) 2-thiophenecarboxylate
Copper(Ⅰ) thiophene-2-carboxylate
Copper(I) thiophene-2-carboxylate
-copper(1+) thiophene-2-carboxylate
Copper(I) thiophene-2-carboxylate≥98%
2-Thiophenecarboxylic Acid Copper(I) Salt
Copper(I) thiophene-2-carboxylate,Cu (TC)
2-Thiophenecarboxylic acid, copper complex
COPPER(I) THIOPHENE-2-CARBOXYLATE ISO 9001:2015 REACH
TIANFU-CHEM__68986-76-5,COPPER(I) THIOPHENE-2-CARBOXYLATE
Copper(I) thiophene-2-carboxylate, may contain approx. 20 wt.% Copper(I) oxide, 95%
Copper(I) thiophene-2-carboxylate, 95%, May contain approx. 20 wt.% Copper(I) oxide
Copper(I) thiophene-2-carboxylate, 90%, May contain approx. 20 wt.% Copper(I) oxide
[EINECS(EC#)]

350-745-9
[Molecular Formula]

C5H3CuO2S
[MDL Number]

MFCD02183524
[MOL File]

68986-76-5.mol
[Molecular Weight]

190.69
Chemical PropertiesBack Directory
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[form ]

Powder
[color ]

Red to brown
[Sensitive ]

Air & Light Sensitive
[Merck ]

14,2521
[InChIKey]

SFJMFSWCBVEHBA-UHFFFAOYSA-M
Safety DataBack Directory
[Hazard Codes ]

Xi,N
[Risk Statements ]

36/37/38-51/53
[Safety Statements ]

26-61
[RIDADR ]

3077
[WGK Germany ]

3
[HazardClass ]

IRRITANT, AIR SENSITIVE, LIGHT SENSITIVE
[HS Code ]

29349990
Hazard InformationBack Directory
[Chemical Properties]

COPPER(I) THIOPHENE-2-CARBOXYLATE is Solid
[Uses]

COPPER(I) THIOPHENE-2-CARBOXYLATE is used for studies of xenobiotic response safener derivatives, synthesis of functionalized BODIPY dye analogs, orthogonal cross-coupling reactions, preparation of parent borondipyrromethene system and Copper mediated cross-coupling.
[Uses]

Mediator in intermolecular cross-coupling reactions, asymmetric 1,4-additions, and allylation reactions.
[Uses]

Reactant or reagent involved in: Studies of xenobiotic response to herbicide safener derivatives; Synthesis of functionalized BODIPY dye analogs; Orthogonal cross-coupling reactions; Preparation of parent borondipyrromethene system; Copper mediated cross-coupling
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