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Merck

474606

Sigma-Aldrich

(S,S)-(+)-N,N′-双(3,5-二-叔丁基亚水杨基)-1,2-环己二胺钴(II)

别名:

(S,S)-Co(salen), (S,S)-Jacobsen HKR catalyst

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About This Item

线性分子式:
[[[(CH3)3C]2C6H2-2-(O-)CH=N]2C6H10]Co
分子量:
603.74
MDL號碼:
分類程式碼代碼:
12352001
PubChem物質ID:
NACRES:
NA.22

mp

>350 °C (lit.)

SMILES 字串

CC(C)(C)c1cc2C=[N@@H]3[C@H]4CCCC[C@@H]4[N@H]5=Cc6cc(cc(c6O[Co]35Oc2c(c1)C(C)(C)C)C(C)(C)C)C(C)(C)C

InChI

1S/C36H54N2O2.Co/c1-33(2,3)25-17-23(31(39)27(19-25)35(7,8)9)21-37-29-15-13-14-16-30(29)38-22-24-18-26(34(4,5)6)20-28(32(24)40)36(10,11)12;/h17-22,29-30,39-40H,13-16H2,1-12H3;/q;+2/p-2/b37-21+,38-22+;/t29-,30-;/m0./s1

InChI 密鑰

ZFWPDJKMASHRPT-IKKUFEJKSA-L

應用

用于末端环氧化物的水解动力学拆分和内消旋环氧化物不对称开环的催化剂。
(S,S)-(+)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II) may be used as a catalyst for the Jacobsen′s hydrolytic kinetic resolution of racemic epoxides, which is a key step during the multi-step synthesis of (+)-patulolide C, macrosphelides(I and G), (-)-(3S,6R)-3,6-dihydroxy-10-methylundecanoic acid, dodoneine, epidodoneine and protein kinase C epsilon (PKCe) inhibitors.

法律資訊

经 Shasun Chemicals and Drugs Limited 授权销售。

儲存類別代碼

11 - Combustible Solids

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

dust mask type N95 (US), Eyeshields, Gloves


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A Concise Synthesis of (-)-(3S, 6R)-3, 6-Dihydroxy-10-methylundecanoic Acid Using a Cross-Metathesis Approach.
Sabitha G, et al.
Synthesis, 2010(07), 1217-1222 (2010)
The enantioselective Diels-Alder reaction of 1-methoxybuta-1, 3-diene with n-butyl glyoxylate catalyzed by the (salen) Cr (III) Cl and Co (II) complexes.
Kwiatkowski P, et al.
Tetrahedron Asymmetry, 15(20), 3189-3194 (2004)
Strategies for the modulation of phase II metabolism in a series of PKCe inhibitors.
Clemens JJ, et al.
Bioorganic & Medicinal Chemistry Letters, 24(15), 3398-3402 (2014)
RCM mediated synthesis of macrosphelides I and G.
Sharma GVM, and Babu KV.
Tetrahedron Asymmetry, 18(18), 2175-2184 (2007)
Total Synthesis of (+)-Dodoneine and Its 6-Epimer.
Sabitha G, et al.
Synthesis, 2009(19), 3285-3292 (2009)

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