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3'-<<<(1,1-dimethylethyl)diphenylsilyl>oxy>methyl>-6',7'-dihydro-1',4,5,6,8,9,9'-heptamethoxy-3-(phenylmethylene)spiro<2H-benzindene-2,8'-<8H>cyclopentisoquinolin>-1(3H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

145222-94-2

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  • 3'-<<<(1,1-dimethylethyl)diphenylsilyl>oxy>methyl>-6',7'-dihydro-1',4,5,6,8,9,9'-heptamethoxy-3-(phenylmethylene)spiro<2H-benzindene-2,8'-<8H>cyclopentisoquinolin>-1(3H)-one

    Cas No: 145222-94-2

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  • 3'-<<<(1,1-dimethylethyl)diphenylsilyl>oxy>methyl>-6',7'-dihydro-1',4,5,6,8,9,9'-heptamethoxy-3-(phenylmethylene)spiro<2H-benzindene-2,8'-<8H>cyclopentisoquinolin>-1(3H)-one

    Cas No: 145222-94-2

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145222-94-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145222-94-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,2,2 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 145222-94:
(8*1)+(7*4)+(6*5)+(5*2)+(4*2)+(3*2)+(2*9)+(1*4)=112
112 % 10 = 2
So 145222-94-2 is a valid CAS Registry Number.

145222-94-2Upstream product

145222-94-2Relevant articles and documents

Total synthesis of crystalline (±)-fredericamycin A. Use of radical spirocyclization

Clive, Derrick L. J.,Tao, Yong,Khodabocus, Ahmad,Wu, Yong-Jin,Angoh, A. Ga?tan,Bennett, Sharon M.,Boddy, Christopher N.,Bordeleau, Luc,Kellner, Dont,Kleiner, Galit,Middleton, Donald S.,Nichols, Christopher J.,Richardson, Scott R.,Vernon, Peter G.

, p. 11275 - 11286 (2007/10/02)

Crystalline (±)-fredericamycin A (1) was synthesized using, as a key step, 5-exo-digonal radical closure of selenide 55. The selenide was generated from the corresponding ketone 54, itself assembled from two components: aldehyde 29 and bromonaphthalene 48

Total Synthesis of (+/-)-Fredericamycin A. Use of Radical Spirocyclization

Clive, Derrick L. J.,Tao, Yong,Khodabocus, Ahmad,Wu, Yong-Jin,Angoh, A. Gaoetan,et al.

, p. 1489 - 1490 (2007/10/02)

(+/-)-Fredericamycin A 1 is synthesized using 5-exo-digonal radical closure of selenide 15 (Scheme 2), and an unusual procedure for both selective demethylation of the advanced intermediate 22 and adjustment of the stereochemistry in the pentadienyl side

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