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((E)-1-methoxy-1-phenylbut-2-ene) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83605-30-5

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83605-30-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83605-30-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,6,0 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 83605-30:
(7*8)+(6*3)+(5*6)+(4*0)+(3*5)+(2*3)+(1*0)=125
125 % 10 = 5
So 83605-30-5 is a valid CAS Registry Number.

83605-30-5Relevant academic research and scientific papers

Efficient assembly of α-aryl and α-vinyl nitriles via iron-catalyzed ether bond activation

Fan, Xiaohui,Guo, Kun,Guan, Yong-Hong,Fu, Lin-An,Cui, Xiao-Meng,Lv, Hao,Zhu, Hong-Bo

supporting information, p. 1068 - 1071 (2014/02/14)

A novel and practical method for the synthesis of diverse α-aryl and α-vinyl nitriles was developed via an iron-catalyzed sp3 C-O ether bond cleavage with C-C bond formation in the reaction of π-activated ethers with TMSCN.

Iron-catalyzed π-activated C-O ether bond cleavage with C-C and C-H bond formation

Fan, Xiaohui,Cui, Xiao-Meng,Guan, Yong-Hong,Fu, Lin-An,Lv, Hao,Guo, Kun,Zhu, Hong-Bo

supporting information, p. 498 - 501 (2014/02/14)

A novel and efficient allylic alkylation reaction between π-activated ethers and allylsilane was realized under mild conditions through iron(III)-catalyzed C sp 3-O ether bond cleavage. The present protocol provides an attractive approach for the construction of sp3-sp3 C-C bonds and can be potentially applied for the selective reduction of benzyl and allyl ethers to their corresponding hydrocarbon compounds by using triethylsilane as a hydride-transfer reagent. A mild, economical, and environmentally friendly method for the construction of C sp 3-C sp 3 bonds through iron-catalyzed π-activated C-O ether bond cleavage is developed. In addition, this catalytic system can be used for the selective reduction of benzylic and allylic C-O ether bonds to C-H bonds. Copyright

Efficient assembly of α-aryl and α-vinyl nitriles via iron-catalyzed ether bond activation

Fan, Xiaohui,Guo, Kun,Guan, Yong-Hong,Fu, Lin-An,Cui, Xiao-Meng,Lv, Hao,Zhu, Hong-Bo

supporting information, p. 1068 - 1071 (2015/02/18)

A novel and practical method for the synthesis of diverse α-aryl and α-vinyl nitriles was developed via an iron-catalyzed sp3 C-O ether bond cleavage with C-C bond formation in the reaction of π-activated ethers with TMSCN.

Iron-Catalyzed π-Activated C-O Ether Bond Cleavage with C-C and C-H Bond Formation

Fan, Xiaohui,Cui, Xiao-Meng,Guan, Yong-Hong,Fu, Lin-An,Lv, Hao,Guo, Kun,Zhu, Hong-Bo

supporting information, p. 498 - 501 (2015/10/05)

A novel and efficient allylic alkylation reaction between π-activated ethers and allylsilane was realized under mild conditions through iron(III)-catalyzed C sp 3-O ether bond cleavage. The present protocol provides an attractive approach for the construction of sp3-sp3 C-C bonds and can be potentially applied for the selective reduction of benzyl and allyl ethers to their corresponding hydrocarbon compounds by using triethylsilane as a hydride-transfer reagent.

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