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2-acetylphenyl 2-chlorobenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84634-61-7

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84634-61-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84634-61-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,6,3 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 84634-61:
(7*8)+(6*4)+(5*6)+(4*3)+(3*4)+(2*6)+(1*1)=147
147 % 10 = 7
So 84634-61-7 is a valid CAS Registry Number.

84634-61-7Relevant academic research and scientific papers

Synthesis of Spiro[benzofuran-2,2'-benzo[b]thiophene]-3,3'-diones via PIDA/CuBr-Mediated Spirocyclization

Du, Yunfei,Li, Xuemin,Liang, Huiyuan,Sun, Fengxia,Wang, Donghua,Wang, Xi,Yang, Yaxin O,Zhang, Jingran

supporting information, p. 6563 - 6569 (2020/11/16)

A phenyliodine(III) diacetate (PIDA)/CuBr-mediated construction of the novel 3H,3'H-spiro[benzofuran-2,2'-benzo[b]thiophene]-3,3'-dione skeleton was realized from the reaction of (Z)-3-hydroxy-1-(2-hydroxyphenyl)-3-(2-halogenphenyl)prop-2-en-1-ones with p

A New Protocol for Total Synthesis of Natural Product Frutinone A and Its Derivatives

Lei, Kang,Sun, Dong-Wei,Tao, Yuan-Yuan,Xu, Xiao-Hua

, p. 98 - 106 (2016/01/26)

A new protocol for total synthesis of natural product frutinone A was accomplished in three steps by using inexpensive 2′-hydroxyacetophenone as starting material. The key intermediate 3-(2-chlorobenzoyl)-4-hydroxycoumarin was synthesized in one pot through Baker-Venkataraman rearrangement of 2-acetylphenyl 2-chlorobenzoate followed by introduction of methyl chloroformate under basic conditions. Then, base-promoted intramolecular nucleophilic substitution reaction of 3-(2-chlorobenzoyl)-4-hydroxycoumarin provided frutinone A in excellent yield. The synthetic route features good yield, transition metal-free and mild reaction conditions, and high tolerance for functionality, thereby allowing easy substitutions around the frutinone A core.

Synthesis and reactivity of 1-aryl-9h-thieno[3,4-b]chromon-9-ones

Krayushkin, Mikhail M.,Levchenko, Konstantin S.,Yarovenko, Vladimir N.,Christoforova, Ludmila V.,Barachevsky, Valery A.,Puankov, Yury A.,Valova, Tatyana M.,Kobeleva, Olga I.,Lyssenko

experimental part, p. 2267 - 2277 (2011/04/23)

Methods were developed for the synthesis of 1-aryl-9H-thieno[3,4-b]chromon- 9-ones based on the reaction of bromo and dibromo derivatives of 2-methyl-4H-chromon-4-one with thioacetamide in DMF. The thienochromones were modified and their fluorescence prop

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