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CAS: 1536473-72-9
中文名称: 
[(2-di-tert-butylphosphino-3,6-dimethoxy-2′,4′,6′-triisopropyl-1,1′-biphenyl)-2-(2′-amino-1,1′-biphenyl)]palladium(ii) methanesulfonate
[(2-二--丁基膦-3,6-二甲氧基-2′,4′,6′-三异丙基-1,1′-联苯)-2-(2′-氨基-1,1′-联苯)] 甲磺酸钯 (ii)
-bubrettphos-pd-g3
英文名称: 
tbubrettphos pd g3
tert-bubrettphos-pd-g3
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货号品牌产品名称规格包装、参考价格详情
46-0325StremMethanesulfonato(2-(di-t-butylphosphino)-3,6-dimethoxy-2',4',6'-tri-i-propyl-1,1'-biphenyl)(2'-amino-1,1'-biphenyl-2-yl)palladium(II), dichloromethane adductmin. 98%834元/100mg;   3090元/500mg;   7680元/2g;   22200元/10g;   展开

Technical Notes:

1.Palladium catalyst used for the arylation of primary amides .

2.Palladium catalyst used for the synthesis of N-aryl carbamates .

3.Palladium catalyst used for the N-monoarylation of amidines.

4. Palladium catalyst used for the cross-coupling of aryl chlorides and triflates with sodium cyanate - a practical synthesis of unsymmetrical ureas .

5. Palladium catalyst used in the synthesis of imidazo4, 5-bpyridines and imidazo4, 5pyrazines through amidation of 2-chloro-3- amino-heterocycles.

6.Palladium catalyst used in the N-arylation of 2- aminothiazoles

7.Palladium catalyst used in the synthesis of diarylethers under mild conditions.

8. Palladium catalyst used in the hydroxylation of aryl and heteroaryl halides.

745979Sigma-AldrichtBuBrettPhos Pd G396%1136.6元/100 MG;   4956.09元/500 MG;   4966.03元/1 G;   6745.65元/2 G;   13535.7元/5 G;   展开

产品说明

一般描述

tBuBrettPhos Pd G3 是第三代 (G3) Buchwald 预催化剂,可用于交叉偶联反应,形成 C-C、C-N、C-O、C-F、C-CF3 和 C-S 键。它具有空气、水分和热稳定性,可溶于多种常见有机溶剂。它具有催化剂用量少、反应时间短、能有效地形成活性物种和精确控制配体钯比等特点。

应用

tBuBrettPhos Pd G3 已被用作在温和反应条件下氨基酸酯与芳基三氟甲磺酸酯的 N -芳基化的预催化剂,且氨基酸酯的消旋作用极小。也可用于在苯甲醛肟作为氢氧化物替代物存在下催化芳基卤化物转化为酚类。

包装

1, 2, 5 g in glass bottle
100, 500 mg in glass bottle

基本信息

经验(实验)分子式C44H62NO5PPdS
分子量854.43
MDL编号MFCD25976528
PubChem化学物质编号329765730
NACRESNA.22

产品性质

质量水平100
测定96%
特点generation 3
reaction suitabilitycore: palladium
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: catalyst
reaction type: Cross Couplings
mp119-131 ℃
官能团phosphine
SMILES stringCOC1=CC=C(OC)C(P(C(C)(C)C)C(C)(C)C)=C1C2=C(C(C)C)C=C(C(C)C)C=C2C(C)C.NC3=C(C4=C([Pd]OS(C)(=O)=O)C=CC=C4)C=CC=C3
InChI1S/C31H49O2P.C12H10N.CH4O3S.Pd/c1-19(2)22-17-23(20(3)4)27(24(18-22)21(5)6)28-25(32-13)15-16-26(33-14)29(28)34(30(7,8)9)31(10,11)12;13-12-9-5-4-8-11(12)10-6-2-1-3-7-10;1-5(2,3)4;/h15-21H,1-14H3;1-6,8-9H,13H2;1H3,(H,2,3,4);/q;;;+1/p-1
InChI keyGAQPAUHHECNHNS-UHFFFAOYSA-M

安全信息

储存分类代码13 - Non Combustible Solids
WGKWGK 3
闪点(F)Not applicable
闪点(C)Not applicable
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