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4-Methoxy-1,1-diphenyl-1-butene is an organic compound with the molecular formula C18H20O. It is a colorless liquid that is soluble in organic solvents and has a molecular weight of 252.35 g/mol. 4-methoxy-1,1-diphenyl-1-butene is characterized by the presence of a 1-butene backbone with a methoxy group at the 4-position and two phenyl rings attached to the terminal carbons. It is synthesized through various chemical reactions and is used in the preparation of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its unique structure, it exhibits specific chemical properties and reactivity, making it a valuable intermediate in organic synthesis.

5558-02-1

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5558-02-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5558-02-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,5 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5558-02:
(6*5)+(5*5)+(4*5)+(3*8)+(2*0)+(1*2)=101
101 % 10 = 1
So 5558-02-1 is a valid CAS Registry Number.

5558-02-1Downstream Products

5558-02-1Relevant academic research and scientific papers

Synthesis of indenes by ytterbium-catalyzed carboalkoxylation/Friedel- Crafts reaction of arylidenecyclopropanes with acetals

Nakamura, Itaru,Kamada, Michiru,Yamamoto, Yoshinori

, p. 2903 - 2906 (2004)

Ytterbium-catalyzed tandem carboalkoxylation/Friedel-Crafts reaction of arylidenecyclopropanes 1 with acetals 2 afforded the corresponding indene derivatives 3 in good to high yields. For example, in the presence of 10mol% of Yb(OTf)3 the react

Enantioselective Oxidative Rearrangements with Chiral Hypervalent Iodine Reagents

Brown, Michael,Kumar, Ravi,Rehbein, Julia,Wirth, Thomas

supporting information, p. 4030 - 4035 (2016/03/16)

A stereoselective hypervalent iodine-promoted oxidative rearrangement of 1,1-disubstituted alkenes has been developed. This practically simple protocol provides access to enantioenriched α-arylated ketones without the use of transition metals from readily

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