所有图片(2)
About This Item
经验公式（希尔记法）:
C8H12BCuF4N4
CAS号:
分子量:
314.56
MDL號碼:
分類程式碼代碼:
12161600
PubChem物質ID:
NACRES:
NA.22
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品質等級
化驗
97%
形狀
solid
反應適用性
core: copper
reagent type: catalyst
環保替代產品特色
Catalysis
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
環保替代類別
SMILES 字串
[Cu+].CC#N.CC#N.CC#N.CC#N.F[B-](F)(F)F
InChI
1S/4C2H3N.BF4.Cu/c4*1-2-3;2-1(3,4)5;/h4*1H3;;/q;;;;-1;+1
InChI 密鑰
YZGSKMIIVMCEFE-UHFFFAOYSA-N
相关类别
一般說明
我们致力于为您提供更环保的替代产品，以符合“绿色化学的12项原则”的一项或多项原则要求。该产品为增强型，提高了催化效率。点击此处以获取更多信息。
應用
Diels-Alder 和 Ullmann 反应中的催化剂，分子内芳香环，甾体中的扩环，烯烃的不对称氮杂环丙烷化，烯丙基卤化物和甲磺酸酯的取代，Kharasch-Sosnovsky 反应。
訊號詞
Danger
危險聲明
危險分類
Skin Corr. 1B
儲存類別代碼
8A - Combustible corrosive hazardous materials
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Paryzek, Z.; Martynow, J.
Journal of the Chemical Society. Perkin Transactions 1, 599-599 (1990)
Kevin M Gillespie et al.
The Journal of organic chemistry, 67(10), 3450-3458 (2002-05-11)
Racemic 2,2'-diamino-6,6'-dimethylbiphenyl is resolved using simulated moving bed chromatography, and the absolute configuration of the enantiomers is confirmed via the X-ray crystal structure of a derivative. The diamine is condensed with a range of aldehydes to give bidentate aldimine proligands
Kerry E Murphy et al.
Organic letters, 7(7), 1255-1258 (2005-03-25)
[reaction: see text] Peptide-based chiral ligands, readily prepared from commercially available materials, are used to promote Cu-catalyzed asymmetric allylic alkylations of alpha,beta-unsaturated esters bearing a gamma-phosphate with various alkylzinc reagents. These transformations lead to the formation of alpha,alpha'-dialkyl-beta,gamma-unsaturated esters in
Le Bras, J.; Muzart, J.
Tetrahedron Letters, 43, 431-431 (2002)
Tobias Schneider et al.
Scientific reports, 9(1), 19991-19991 (2019-12-29)
Ubiquitylation is an eminent posttranslational modification referring to the covalent attachment of single ubiquitin molecules or polyubiquitin chains to a target protein dictating the fate of such labeled polypeptide chains. Here, we have biochemically produced artificially Lys11-, and Lys27-, and
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