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アッセイ
≥95%
フォーム
powder
保管温度
−20°C
InChI
1S/C19H29NO4/c1-5-23-18(21)15-12(3)20-13(4)16(19(22)24-6-2)17(15)14-10-8-7-9-11-14/h14,17,20H,5-11H2,1-4H3
InChI Key
GERWBKSVDHUVIT-UHFFFAOYSA-N
アプリケーション
Diethyl-4-cyclohexyl-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate was reported to chemoselectively modify histidine under visible light where the unsubstituted nitrogen groups on the modified His imidazole are conserved. Diethyl-4-cyclohexyl-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate is also a versitile reagent for photoredox chemistry.
Product can be used with our line of photoreactors: Including Penn PhD (Z744035) & SynLED 2.0 (Z744080)
Product can be used with our line of photoreactors: Including Penn PhD (Z744035) & SynLED 2.0 (Z744080)
その他情報
Histidine-specific peptide modification via visible-light-promoted C-H alkylation
Open-Air Alkylation Reactions in Photoredox-Catalyzed DNA-Encoded Library Synthesis
A photocatalyst-free photo-induced denitroalkylation of ß-nitrostyrenes with 4-alkyl substituted Hantzsch esters at room temperature
Intermolecular Radical Addition to Ketoacids Enabled by Boron Activation
Oxa- and Azabenzonorbornadienes as Electrophilic Partners under Photoredox/Nickel Dual Catalysis
Exploration of a chiral cobalt catalyst for visible-light-induced enantioselective radical conjugate addition
Open-Air Alkylation Reactions in Photoredox-Catalyzed DNA-Encoded Library Synthesis
A photocatalyst-free photo-induced denitroalkylation of ß-nitrostyrenes with 4-alkyl substituted Hantzsch esters at room temperature
Intermolecular Radical Addition to Ketoacids Enabled by Boron Activation
Oxa- and Azabenzonorbornadienes as Electrophilic Partners under Photoredox/Nickel Dual Catalysis
Exploration of a chiral cobalt catalyst for visible-light-induced enantioselective radical conjugate addition
シグナルワード
Warning
危険有害性情報
危険有害性の分類
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
ターゲットの組織
Respiratory system
保管分類コード
11 - Combustible Solids
WGK
WGK 3
引火点(°F)
Not applicable
引火点(℃)
Not applicable
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Jan Code
916080-VAR:
916080-BULK:
916080-100MG:
最新バージョンのいずれかを選択してください：
Jie Wang et al.
The Journal of organic chemistry, 84(23), 15315-15322 (2019-11-02)
Highly efficient alkylation of β-chloro ketones and their derivatives was achieved by means of domino dehydrochlorination/Mn-enabled radical-based alkyl-alkyl cross-coupling reaction. In situ-generated α,β-unsaturated ketones and their analogues were identified as the reaction intermediates. Known bioactive compounds, such as melperone and
Shasha Xie et al.
Journal of the American Chemical Society, 141(41), 16237-16242 (2019-10-02)
The intermolecular radical addition to the carbonyl group is difficult due to the facile fragmentation of the resulting alkoxyl radical. To date, the intermolecular radical addition to ketones, a valuable approach to construct quaternary carbon centers, remains a formidable synthetic
Xuefeng Wang et al.
Chemical communications (Cambridge, England), 55(14), 2062-2065 (2019-01-29)
A three-component reaction between 4-substituted Hantzsch esters, DABCO·(SO2)2, and vinyl azides in the presence of photoredox catalysts under visible light irradiation is developed. Substituted Hantzsch esters as radical reservoirs are used in the reaction between sulfur dioxide and vinyl azides.
Kai Zhang et al.
Angewandte Chemie (International ed. in English), 58(38), 13375-13379 (2019-07-12)
Chiral catalysts tolerating photochemical reactions are in great demand for the vast development of visible-light-induced asymmetric synthesis. Now, chiral octahedral complexes based on earth-abundant metal and chiral N4 ligands are reported. One well-defined chiral CoII -complex is shown to be
Kazunari Nakajima et al.
Organic letters, 21(12), 4642-4645 (2019-05-31)
Introduction of alkyl groups on azodicarboxylate esters is an important method to prepare alkyl amine derivatives. Herein, we report reactions of 4-alkyl-1,4-dihydropyridines as alkylation reagents with di- tert-butyl azodicarboxylate to prepare alkyl amine derivatives under heating conditions. The alkylation reactions
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