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Benzene, [3-(1-methylethoxy)-1-propenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13645-20-0

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13645-20-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13645-20-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,4 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13645-20:
(7*1)+(6*3)+(5*6)+(4*4)+(3*5)+(2*2)+(1*0)=90
90 % 10 = 0
So 13645-20-0 is a valid CAS Registry Number.

13645-20-0Relevant academic research and scientific papers

Transfer hydrogenation of cinnamaldehyde with 2-propanol on Al2O3 and SiO2-Al2O3 catalysts: Role of Lewis and Br?nsted acidic sites

Gao, Zhan-Kun,Hong, Yong-Chun,Hu, Zhun,Xu, Bo-Qing

, p. 4511 - 4519 (2017)

Transfer hydrogenation of α,β-unsaturated aldehyde is an important reaction (MPV reaction) for the synthesis of allyl alcohol because of its high selectivity for the hydrogenation of the carbonyl group. This reaction can proceed over many oxide catalysts

Electrochemical properties and reactions of organoboronic acid esters containing unsaturated bonds at their α-position

Ohtsuka, Kazuhiro,Inagi, Shinsuke,Fuchigami, Toshio

, p. G23 - G28 (2017/12/26)

Electrochemical analyses of 2-(cynnamyl)boronic acid pinacol ester and (3-phenyl-2-propynyl)boronic acid pinacol ester, and their trimethylsilyl analogues as well as their parent compounds were comparatively studied by cyclic voltammetry measurements. We

Gold-catalyzed hydrofunctionalization of allenes with nitrogen and oxygen nucleophiles and its mechanistic insight

Nishina, Naoko,Yamamoto, Yoshinori

experimental part, p. 1799 - 1808 (2009/06/28)

A wide range of nucleophiles, such as amines and alcohols, reacted intermolecularly with various allenes in the presence of gold catalysts to give the corresponding hydrofunctionalization products in high yields. The intermolecular hydroamination of chira

Transetherification of allylic and benzylic ethers in the presence of ferric ion

Salehi, Peyman,Irandoost, Mohsen,Seddighi, Behnam,Kargar Behbahani, Farahnaz,Tahmasebi, Daryush Poor

, p. 1743 - 1747 (2007/10/03)

Alcoholysis of allylic, secondary and tertiary benzylic ethers is proceeded efficiently in the presence of catalytic amounts of ferric ion as anhydrous FeCl3 and Fe(ClO4)3.

Selective and efficient alcoholyses of allylic, secondary- and tertiary benzylic alcohols in the presence of iron(III)

Salehi, Peyman,Iranpoor, Nasser,Behbahani, Farahnaz Kargar

, p. 943 - 948 (2007/10/03)

An efficient and selective method for the conversion of allylic, secondary- and tertiary benzylic alcohols into their corresponding ethers in the presence of iron(III) as FeCl3 and Fe(ClO4)3 under solvolytic condition is d

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