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108664-84-2

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108664-84-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108664-84-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,6,6 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 108664-84:
(8*1)+(7*0)+(6*8)+(5*6)+(4*6)+(3*4)+(2*8)+(1*4)=142
142 % 10 = 2
So 108664-84-2 is a valid CAS Registry Number.

108664-84-2Relevant academic research and scientific papers

Synthesis, crystal structure and theoretical calculation of triphenyltin (IV) polymer based on 2,4-dichlorophenylacrylic acid

Han, Shuang,Wang, He,Wang, Jiajun,Dun, Linan,Li, Chuanbi,Liu, Chunling

, p. 187 - 193 (2020)

Reaction between 2,4-dichlorophenylacrylic acid (HL) and triphenyltin (IV) hydroxide to yield the complex [(Ph3Sn)L]n (1). The complex has been characterized by elemental analysis, infrared spectrum and single crystal X-ray diffracti

Cobalt-Catalyzed Vinylic C-H Addition to Formaldehyde: Synthesis of Butenolides from Acrylic Acids and HCHO

Yu, Shuling,Hong, Chao,Liu, Zhanxiang,Zhang, Yuhong

supporting information, p. 8359 - 8364 (2021/11/01)

A carboxyl-assisted C-H functionalization of acrylic acids with formaldehyde to give butenolides is described. It is the first time that the addition of an inert vinylic C-H bond to formaldehyde has been achieved via cobalt-catalyzed C-H activation. The unique reactivity of the cobalt species was observed when compared with related Rh or Ir catalysts. γ-Hydroxymethylated butenolides were produced by the treatment of Na2CO3 after the catalytic reaction in one pot.

Synthesis and Antifungal Activity of a Series of Novel 1,2-Disubstituted Propenones

Ogata, Masaru,Matsumoto, Hiroshi,Kida, Shiro,Shimizu, Sumio,Tawara, Katsuya,Kawamura, Yoshimi

, p. 1497 - 1502 (2007/10/02)

To find an antifungal agent other than those of the imidazole and triazole series, a new class of 1,2-disubstituted propenones I and II was prepared and tested for antifungal activity.Comparison of the structure-activity relationships showed that the conjugated structure of carbonyl and exomethylene groups in I and II plays an important role in potent antifungal acivity.However, it is noteworthy that compounds 53, 54, and 56, which have a hydroxymethyl or methoxymethyl group instead of an exo-methylene group in I, also showed potent activity.Although many compounds exhibited strong antifungal activity in vitro, none showed activity in vivo of oral efficacy against subacute systemic candidiasis in mice. '

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