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1-(2,4-dichlorophenyl)-3-buten-1-yl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

132587-11-2

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132587-11-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132587-11-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,5,8 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 132587-11:
(8*1)+(7*3)+(6*2)+(5*5)+(4*8)+(3*7)+(2*1)+(1*1)=122
122 % 10 = 2
So 132587-11-2 is a valid CAS Registry Number.

132587-11-2Relevant academic research and scientific papers

Indium-mediated one-pot, three-component synthesis of homoallyl alcohol esters without catalysts and dehydrants

Du, Zhengyin,Li, Yanchun,Wang, Fen,Zhou, Wanwei,Wang, Jin-Xian

supporting information; experimental part, p. 1745 - 1747 (2010/05/18)

Indium-mediated one-pot esterification reaction of acyl chlorides or anhydride by using in situ-prepared homoallyl alcohols from aromatic aldehydes and allyl bromide proceeded smoothly to afford the corresponding homoallyl alcohol esters in high yields within about 1 h, which provided a simple and efficient protocol for the simultaneous allylation and esterification of aldehydes without other catalysts and dehydrants.

LiBF4-Catalyzed three-component coupling of an aldehyde, acetic anhydride and allyltrimethylsilane/TMSCN

Yadav,Reddy, B.V. Subba,Vishnumurthy,Chary, Ch. Janardhana

, p. 5915 - 5918 (2008/02/10)

Lithium tetrafluoroborate is found to be an efficient catalyst for allylation and cyanation of aldehydes with allyltrimethylsilane and trimethylsilyl cyanide in the presence of acetic anhydride at room temperature to produce homoallylic acetates and α-cya

Indium(III) chloride catalyzed allylation of gem-diacetates: A facile synthesis of homoallyl acetates

Yadav,Subba Reddy,Madhuri,Sabitha

, p. 18 - 19 (2007/10/03)

Indium(III) chloride is found to catalyze efficiently the allylation of gem-diacetates with allyltrimethylsilane at room temperature to afford the corresponding homoallylic acetates in high yields with good regioselectivity.

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