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{η4-2-(α,α-diethoxybenzyl)-1,3-butadiene}tricarbonyliron(0) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

128091-56-5

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128091-56-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128091-56-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,0,9 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 128091-56:
(8*1)+(7*2)+(6*8)+(5*0)+(4*9)+(3*1)+(2*5)+(1*6)=125
125 % 10 = 5
So 128091-56-5 is a valid CAS Registry Number.

128091-56-5Upstream product

128091-56-5Downstream Products

128091-56-5Relevant academic research and scientific papers

Organische Synthesen mit Uebergangsmetallkomplexen XXXVIII +. Umwandlung von Tri(methylen)methan- in 1,3-Dienliganden an Chrom- und Eisenkomplexen

Aumann, Rudolf,Trentmann, Beate

, p. 171 - 184 (1989)

1,3-Diene complexes and 1,3-dienes have been obtained from tri(methylene)-methane complexes Ln-1M (III) of chromium and iron n-1M = Cr(CO)4, Fe(CO)3; Y = OH, CO2Et, CH2OH> by transformation of the α-CH2Y moiety into terminal =CH2 and =CHY groups, respectively.The transformation of CH2Y into a =CH2 group can be achieved by a suprafacial nucleophilic 1,4-substitution of Y.A transformation of CH2Y into =CHY takes place by metal-induced 1,4-hydrogen transfer.The iron complex IIIa undergoes (acid-catalyzed) nucleophilic 1,4- and 1,1-substitution reactions, respectively.Thus, from diastereomers IIIaA and B the 2-benzyl-1,3-diene complex VIII is obtained by 1,4-substitution, whereas diastereomer IIIaC gives a tri(methylene)methane complex (IX) by a 1,1-substitution without undergoing a change in its configuration.The corresponding chromium complex IIIdA under protic conditions yields the (metalfree) dienes XI and XII.By contrast, the chromium complexes IIId-f at 50 deg C in inert solvents yield 3-benzyl-1,3-dienes (Va-c) and 3-methyl-1,3-dienes (V' a-c) by metal-induced 1,4-hydrogen shifts.The corresponding enols Va and V' a (Y = OH) rearrange immediately to give the aldehydes VI, VI' and VII.

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