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84092-45-5

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84092-45-5 Usage

Preparation

Obtained by reaction of prenyl bromide with 2-hydroxy-4,6-di- (methoxymethoxy)aceto-phenone in methanolic potassium hydroxide solution, first at 0°, then at r.t. for 24 h (74%).

Check Digit Verification of cas no

The CAS Registry Mumber 84092-45-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,0,9 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 84092-45:
(7*8)+(6*4)+(5*0)+(4*9)+(3*2)+(2*4)+(1*5)=135
135 % 10 = 5
So 84092-45-5 is a valid CAS Registry Number.

84092-45-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[2-hydroxy-4,6-bis(methoxymethoxy)-3-(3-methylbut-2-en-1-yl)phenyl]ethanone

1.2 Other means of identification

Product number -
Other names 2-hydroxy-4,6-di(methoxymethoxy)-3-C-prenylacetophenone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:84092-45-5 SDS

84092-45-5Relevant articles and documents

Magnesium dicarboxylates promote the prenylation of phenolics that is extended to the total synthesis of icaritin

Fu, Xuewen,Lu, Xiaoxia,Wang, Chun,Wen, Yongju,Xiong, Wei,Zhang, Guolin,Zhang, Jichao

, p. 1117 - 1124 (2022/02/16)

The prenylation of phenolic substrates promoted by magnesium dicarboxylates was developed. An investigation of the scope demonstrated that substrates with electron-donating group(s) gave better yields than those with electron-withdrawing group(s). Althoug

Total Synthesis and in Vitro Anti-Tumor-Promoting Activities of Racemic Acetophenone Monomers from Acronychia trifoliolata

Morita, Chihiro,Kobayashi, Yukiko,Saito, Yohei,Miyake, Katsunori,Tokuda, Harukuni,Suzuki, Nobutaka,Ichiishi, Eiichiro,Lee, Kuo-Hsiung,Nakagawa-Goto, Kyoko

, p. 2890 - 2897 (2016/12/07)

Six acetophenone derivatives, acronyculatins I (1), J (2), K (3), L (4), N (5), and O (6), were recently isolated from Acronychia trifoliolata, and the structure of the known acronyculatin B (7) was revised. Because of the limited quantities of isolated p

Identification of SVM-based classification model, synthesis and evaluation of prenylated flavonoids as vasorelaxant agents

Dong, Xiaowu,Liu, Yujie,Yan, Jingying,Jiang, Chaoyi,Chen, Jing,Liu, Tao,Hu, Yongzhou

scheme or table, p. 8151 - 8160 (2009/04/11)

Support vector machine (SVM) was applied to predict vasorelaxation effect of different structural molecules. A good classification model had been established, and the accuracy in prediction for the training, test, and overall datasets was 93.0%, 82.6%, an

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