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2,2-dichloro-7,7a-dihydro-2aH-cyclobuta[a]inden1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20429-38-3

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20429-38-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20429-38-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,4,2 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 20429-38:
(7*2)+(6*0)+(5*4)+(4*2)+(3*9)+(2*3)+(1*8)=83
83 % 10 = 3
So 20429-38-3 is a valid CAS Registry Number.

20429-38-3Relevant academic research and scientific papers

Free radical-based annulation of alkenes yielding fused cycloheptanones

Zhang, Wei,Hua, Ye,Hoge, Garrett,Dowd, Paul

, p. 3865 - 3868 (1994)

Stereospecific annulation of cyclic alkenes for the preparation of cis-fused seven-membered ring systems was accomplished by sequential [2+2] cycloaddition, exo-allylation, hydrohalogenation, and free radical ring expansion. The new strategy extends our recently developed cyclobutanone-based ring expansion reactions.

Synthesis of Highly Substituted Cyclopropanes via the Quasi-Favorskii Rearrangement of α,α-Dichlorocyclobutanols

Behnke, Nicole Erin,Siitonen, Juha H.,Chamness, Stephen A.,Kürti, László

supporting information, p. 5715 - 5720 (2020/05/22)

A method for the synthesis of highly substituted cyclopropanes via a quasi-Favorskii rearrangement is described. The method includes the combination two chemical transformations starting from α,α-dichlorocyclobutanones prepared via the [2 + 2] Staudinger ketene cycloaddition between either terminal- or cis-olefins and dichloroketene. First, α,α-dichlorocyclobutanones are reacted with organocerium reagents to afford the corresponding tertiary alcohols in good to excellent yields through a nucleophilic addition reaction that provided exclusively anti-products. Second, upon irreversible deprotonation, the tertiary α,α-dichlorocyclobutanols underwent a ring-contraction reaction (i.e., quasi-Favorskii rearrangement) to form structurally diverse cyclopropanes in moderate to good yields. The syn-stereoselectivity during the quasi-Favorskii rearrangement was evaluated using DFT analysis.

GERMINATION PROMOTERS

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Page/Page column 24, (2018/09/12)

The present invention relates to new compounds of formula (I) for the promotion of seed germination, to processes for preparing the compounds, to seeds comprising the compounds, to seed germination promoting compositions comprising the compounds and to methods of using the compounds for promoting the germination of seeds. In particular, the compounds are useful in promoting germination of corn under cold stress conditions.

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