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Phosphonic acid, [(2E)-1-(benzoyloxy)-3-phenyl-2-propenyl]-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

185301-51-3

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185301-51-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 185301-51-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,3,0 and 1 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 185301-51:
(8*1)+(7*8)+(6*5)+(5*3)+(4*0)+(3*1)+(2*5)+(1*1)=123
123 % 10 = 3
So 185301-51-3 is a valid CAS Registry Number.

185301-51-3Downstream Products

185301-51-3Relevant academic research and scientific papers

Three-Component Coupling of Acylphosphonates and Two Carbonyl Compounds Promoted by Low-Valent Samariums: One-Pot Synthesis of β-Hydroxyphosphonates

Takaki, Ken,Itono, Yuichiro,Nagafuji, Akihiro,Naito, Yoji,Shishido, Tetsuya,Takehira, Katsuomi,Makioka, Yoshikazu,Taniguchi, Yuki,Fujiwara, Yuzo

, p. 475 - 481 (2007/10/03)

Three-component coupling of acylphosphonates and two carbonyl compounds leading to β-hydroxyphosphonates has been achieved with low-valent samariums. Thus, acylphosphonates reacted with aldehydes in the presence of semicatalytic amounts of samarium metal or SmI2 to give acyloxyphosphonates in good yields. The second coupling reaction of the acyloxyphosphonates with aldehydes or ketones promoted by SmI2 afforded β-hydroxyphosphonates instead of olefins. Moreover, these two reactions could be carried out in one pot.

Asymmetric dihydroxylation of 1-acyloxy-2(E)-alkenylphosphonates with AD-mix reagents. Effects of 1-acyloxy functional groups on the asymmetric dihydroxylation

Yokomatsu, Tsutomu,Yamagishi, Takehiro,Sada, Tomoyuki,Suemune, Kenji,Shibuya, Shiroshi

, p. 781 - 790 (2007/10/03)

Asymmetric dihydroxylation (AD) of a racemic mixture of 1-acyloxy-2(E)- alkenylphosphonates with AD-mix-α or -β reagents was examined. The kinetic rate of dihydroxylation was highly dependent upon the configuration of the 1- acyloxy functional group as we

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