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Merck

Z742680

SynLED Parallel Photoreactor

동의어(들):

parallel photoreactor

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제품정보 (DICE 배송 시 비용 별도)

UNSPSC Code:
12352300
기술 서비스
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도움 문의


AC/DC input

, universal plug set (included), 100 - 240 V AC, 50/60 Hz

feature

capacity 16  vial(s)

reaction suitability

reagent type: catalyst
reaction type: Photocatalysis

parameter

465-470 nm spectral range

General description

This newly designed photoreactor enables simple small-scale photocatalysis reaction screening ensuring high levels of consistency across reactions and between runs.

Features and Benefits

  • Bottom-lit LEDs (465-470 nm) across a 4x4 reaction block array provides consistent light intensity (130-140 lm) and angle (45°)
  • Built-in cooling fan provides consistent temperature to each parallel reaction
  • Uses 1-2 dram scintillation vials or microwave vials (O.D. of 1.7 cm or less)
  • Power supply is wall plug power supply 700mA 12 W
  • Compatible with IKA magnetic stirrer with round plate (Z645052)
  • Compatible with liquid scintillation vials (8 mL Wheaton, Z188719)




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시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리 방문


문서

Learn about the applications of chiral oxazaborolidinium ions (COBIs) as Lewis acid catalysts in different asymmetric reactions such as cyclopropanation, epoxidation, and radical reactions along with details of their catalytic action.

This article details the latest progress in synthesizing alkylsulfonyl fluorides through different approaches that utilize photoredox catalysis, electrocatalysis, transition-metal catalysis, and organocatalysis. The alkylsulfonyl fluorides thus prepared could be utilized further in sulfur(VI) fluoride exchange (SuFEx) click reactions.

This review provides a summary of recent approaches in developing green methods for visible-light-mediated reactions that operate under mild conditions and avoid the need for toxic transition-metal catalysts or harsh reaction conditions.

모든 기사 보기

관련 콘텐츠

Photoredox catalysis utilizes photocatalysts in the presence of visible light to form an array of synthetic transformations including, but not limited to, cross-coupling, C-H functionalization, alkene and arene functionalization, and trifluoromethylation.





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SKUGTIN
Z742680-1EA04061838663863