762504
Bis[(tetrabutylammonium iodide)copper(I) iodide]
95%
Manufacturer: Sigma Aldrich
Synonym(S): Tetrabutylammonium iodide copper(I) iodide dimer
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 1 G | 762504-1-G | In Stock | ₹ 7,790.00 |
| 5 G | 762504-5-G | In Stock | ₹ 16,656.00 |
762504 - 1 G
In Stock
Quantity
1
Base Price: ₹ 7,790.00
GST (18%): ₹ 1,402.20
Total Price: ₹ 9,192.20
Quality Level
100
Assay
95%
form
solid
reaction suitability
core: copperreagent type: catalyst
mp
90-97 °C
SMILES string
[I-].[I-].[Cu]I.[Cu]I.CCCC[N+](CCCC)(CCCC)CCCC.CCCC[N+](CCCC)(CCCC)CCCC
InChI
1S/2C16H36N.2Cu.4HI/c2*1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;;;;;;/h2*5-16H2,1-4H3;;;4*1H/q4*+1;;;;/p-4
InChI key
AVVGGLORWAVEFH-UHFFFAOYSA-J
Related Products
Description
- Application: Bis[(tetrabutylammonium iodide)copper(I) iodide] can be used as a catalyst:To synthesize 1,4-disubstituted 1,2,3-triazoles via three-component click reaction[1].For the N-arylation of indoles in the presence of potassium carbonate as a base[2].In the Ullmann coupling reaction in the presence of cesium carbonate and acetonitrile[3].
SAFETY INFORMATION
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Compare Similar Items
Show Difference
Quality Level: 100
Assay: 95%
form: solid
reaction suitability: core: copperreagent type: catalyst
mp: 90-97 °C
SMILES string: [I-].[I-].[Cu]I.[Cu]I.CCCC[N+](CCCC)(CCCC)CCCC.CCCC[N+](CCCC)(CCCC)CCCC
InChI: 1S/2C16H36N.2Cu.4HI/c2*1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;;;;;;/h2*5-16H2,1-4H3;;;4*1H/q4*+1;;;;/p-4
InChI key: AVVGGLORWAVEFH-UHFFFAOYSA-J
Quality Level:
100
Assay:
95%
form:
solid
reaction suitability:
core: copperreagent type: catalyst
mp:
90-97 °C
SMILES string:
[I-].[I-].[Cu]I.[Cu]I.CCCC[N+](CCCC)(CCCC)CCCC.CCCC[N+](CCCC)(CCCC)CCCC
InChI:
1S/2C16H36N.2Cu.4HI/c2*1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;;;;;;/h2*5-16H2,1-4H3;;;4*1H/q4*+1;;;;/p-4
InChI key:
AVVGGLORWAVEFH-UHFFFAOYSA-J
Quality Level: 100
Assay: __
form: solid
reaction suitability: __
mp: 57-77 °C
SMILES string: OB(O)C1=Cc2ccccc2C1
InChI: 1S/C9H9BO2/c11-10(12)9-5-7-3-1-2-4-8(7)6-9/h1-5,11-12H,6H2
InChI key: VBMIZCKXRRAXBK-UHFFFAOYSA-N
Quality Level:
100
Assay:
__
form:
solid
reaction suitability:
__
mp:
57-77 °C
SMILES string:
OB(O)C1=Cc2ccccc2C1
InChI:
1S/C9H9BO2/c11-10(12)9-5-7-3-1-2-4-8(7)6-9/h1-5,11-12H,6H2
InChI key:
VBMIZCKXRRAXBK-UHFFFAOYSA-N
Quality Level: 100
Assay: __
form: solid
reaction suitability: core: palladiumreaction type: Buchwald-Hartwig Cross Coupling Reactionreaction type: Heck Reactionreaction type: Hiyama Couplingreaction type: Negishi Couplingreaction type: Sonogashira Couplingreaction type: Stille Couplingreaction type: Suzuki-Miyaura Couplingreagent type: ligandreagent type: ligandreaction type: Cross Couplings
mp: 130-136 °C (decomposition)
SMILES string: CS(=O)(=O)O[Pd]c1ccccc1-c2ccccc2N.CC34CC5(C)OC(C)(CC(C)(O3)P5c6ccccc6)O4
InChI: 1S/C16H21O3P.C12H10N.CH4O3S.Pd/c1-13-10-15(3)19-14(2,17-13)11-16(4,18-13)20(15)12-8-6-5-7-9-12;13-12-9-5-4-8-11(12)10-6-2-1-3-7-10;1-5(2,3)4;/h5-9H,10-11H2,1-4H3;1-6,8-9H,13H2;1H3,(H,2,3,4);/q;;;+1/p-1
InChI key: PBZIJOKKZYPPSJ-UHFFFAOYSA-M
Quality Level:
100
Assay:
__
form:
solid
reaction suitability:
core: palladiumreaction type: Buchwald-Hartwig Cross Coupling Reactionreaction type: Heck Reactionreaction type: Hiyama Couplingreaction type: Negishi Couplingreaction type: Sonogashira Couplingreaction type: Stille Couplingreaction type: Suzuki-Miyaura Couplingreagent type: ligandreagent type: ligandreaction type: Cross Couplings
mp:
130-136 °C (decomposition)
SMILES string:
CS(=O)(=O)O[Pd]c1ccccc1-c2ccccc2N.CC34CC5(C)OC(C)(CC(C)(O3)P5c6ccccc6)O4
InChI:
1S/C16H21O3P.C12H10N.CH4O3S.Pd/c1-13-10-15(3)19-14(2,17-13)11-16(4,18-13)20(15)12-8-6-5-7-9-12;13-12-9-5-4-8-11(12)10-6-2-1-3-7-10;1-5(2,3)4;/h5-9H,10-11H2,1-4H3;1-6,8-9H,13H2;1H3,(H,2,3,4);/q;;;+1/p-1
InChI key:
PBZIJOKKZYPPSJ-UHFFFAOYSA-M
Quality Level: 100
Assay: 95%
form: solid
reaction suitability: core: palladiumreaction type: Buchwald-Hartwig Cross Coupling Reactionreaction type: Heck Reactionreaction type: Hiyama Couplingreaction type: Negishi Couplingreaction type: Sonogashira Couplingreaction type: Stille Couplingreaction type: Suzuki-Miyaura Couplingreagent type: catalystreaction type: Cross Couplings
mp: 195-197 °C (decomposition)
SMILES string: CS(=O)(=O)O[Pd]c1ccccc1-c2ccccc2N.COc3ccc(OC)c(c3P(c4cc(cc(c4)C(F)(F)F)C(F)(F)F)c5cc(cc(c5)C(F)(F)F)C(F)(F)F)-c6c(cc(cc6C(C)C)C(C)C)C(C)C
InChI: 1S/C39H37F12O2P.C12H10N.CH4O3S.Pd/c1-19(2)22-11-29(20(3)4)33(30(12-22)21(5)6)34-31(52-7)9-10-32(53-8)35(34)54(27-15-23(36(40,41)42)13-24(16-27)37(43,44)45)28-17-25(38(46,47)48)14-26(18-28)39(49,50)51;13-12-9-5-4-8-11(12)10-6-2-1-3-7-10;1-5(2,3)4;/h9-21H,1-8H3;1-6,8-9H,13H2;1H3,(H,2,3,4);/q;;;+1/p-1
InChI key: LLXGRQGGARSAOC-UHFFFAOYSA-M
Quality Level:
100
Assay:
95%
form:
solid
reaction suitability:
core: palladiumreaction type: Buchwald-Hartwig Cross Coupling Reactionreaction type: Heck Reactionreaction type: Hiyama Couplingreaction type: Negishi Couplingreaction type: Sonogashira Couplingreaction type: Stille Couplingreaction type: Suzuki-Miyaura Couplingreagent type: catalystreaction type: Cross Couplings
mp:
195-197 °C (decomposition)
SMILES string:
CS(=O)(=O)O[Pd]c1ccccc1-c2ccccc2N.COc3ccc(OC)c(c3P(c4cc(cc(c4)C(F)(F)F)C(F)(F)F)c5cc(cc(c5)C(F)(F)F)C(F)(F)F)-c6c(cc(cc6C(C)C)C(C)C)C(C)C
InChI:
1S/C39H37F12O2P.C12H10N.CH4O3S.Pd/c1-19(2)22-11-29(20(3)4)33(30(12-22)21(5)6)34-31(52-7)9-10-32(53-8)35(34)54(27-15-23(36(40,41)42)13-24(16-27)37(43,44)45)28-17-25(38(46,47)48)14-26(18-28)39(49,50)51;13-12-9-5-4-8-11(12)10-6-2-1-3-7-10;1-5(2,3)4;/h9-21H,1-8H3;1-6,8-9H,13H2;1H3,(H,2,3,4);/q;;;+1/p-1
InChI key:
LLXGRQGGARSAOC-UHFFFAOYSA-M