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8-benzoyl-1,3,7-trimethyl-3,7-dihydro-1H-purine-2,6-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100201-52-3

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100201-52-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100201-52-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,2,0 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 100201-52:
(8*1)+(7*0)+(6*0)+(5*2)+(4*0)+(3*1)+(2*5)+(1*2)=33
33 % 10 = 3
So 100201-52-3 is a valid CAS Registry Number.

100201-52-3Downstream Products

100201-52-3Relevant academic research and scientific papers

REACTION OF 1,3-DIMETHYLURACIL, 1,3-DIMETHYLTHYMINE, AND CAFFEINE WITH CARBON RADICALS

Itahara, Toshio,Seto, Yuichi

, p. 1441 - 1442 (1985)

Reaction of 1,3-dimethyluracil, 1,3-dimethylthymine, and caffeine with carbon radicals formed on treatment of carboxylic acids, silver nitrate, and ammonium peroxodisulfate was investigated.

Aromatization as an Impetus to Harness Ketones for Metallaphotoredox-Catalyzed Benzoylation/Benzylation of (Hetero)arenes

Lee, Shao-Chi,Li, Li-Yun,Tsai, Zong-Nan,Lee, Yi-Hsin,Tsao, Yong-Ting,Huang, Pin-Gong,Cheng, Cheng-Ku,Lin, Heng-Bo,Chen, Ting-Wei,Yang, Chung-Hsin,Chiu, Cheng-Chau,Liao, Hsuan-Hung

, p. 85 - 89 (2022/01/04)

Herein we report ketones as feedstock materials in radical cross-coupling reactions under Ni/photoredox dual catalysis. In this approach, simple condensation first converts ketones into prearomatic intermediates that then act as activated radical sources for cross-coupling with aryl halides. Our strategy enables the direct benzylation/benzoylation of (hetero)arenes under mild reaction conditions with high functional group tolerance.

Visible-Light-Triggered, Metal- and Photocatalyst-Free Acylation of N-Heterocycles

Guillemard, Lucas,Colobert, Fran?oise,Wencel-Delord, Joanna

supporting information, p. 4184 - 4190 (2018/09/25)

A photoinduced acylation of N-heterocycles is explored. This visible-light triggered reaction occurs not only under extremely mild reaction conditions, but also does not require the presence of a photosensitizer. The mechanistic studies suggest formation of EDA complexes prompt to harness the energy from visible-light. Compatibility with a large panel of α-keto acids as acyl precursors and an array of N-heterocycles clearly showcase the synthetic potential of this handy and green acylation protocol. (Figure presented.).

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