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4-acetoxy-2-methylbenzaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

120802-53-1

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120802-53-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120802-53-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,8,0 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 120802-53:
(8*1)+(7*2)+(6*0)+(5*8)+(4*0)+(3*2)+(2*5)+(1*3)=81
81 % 10 = 1
So 120802-53-1 is a valid CAS Registry Number.

120802-53-1Downstream Products

120802-53-1Relevant academic research and scientific papers

SUBSTITUENT EFFECTS ON THE PHOTOCHEMISTRY OF o-TOLUALDEHYDES

Charlton, James L.,Koh, Kevin

, p. 5595 - 5598 (1988)

The effect of 4-oxy and 4,5-dioxy substituents on the photochemical conversion of 2-methylbenzaldehydes to o-quinodimethanes (o-QDMs) has been studied.The presence of a 4-methoxy, or a 4 and 5-methoxy substituent prevented the photochemical formation of the o-QDM whereas 4-acetoxy and 4,5-diacetoxy-2-methylbenzaldehyde and the corresponding mesylates and tosylates were successfully converted to the o-QDMs.

One-Pot, Enantioselective Synthesis of 2,3-Dihydroazulen-6(1H)-one: A Concise Access to the Core Structure of Cephalotaxus Norditerpenes

Yongsheng, Zheng,Ghazvini Zadeh, Ebrahim H.,Yuan, Yu

supporting information, p. 2115 - 2119 (2016/05/09)

A one-pot enantioselective synthesis of cis-substituted 2,3-dihydroazulen-6(1H)-one is described. In this cascade reaction, an organocatalyzed asymmetric Michael reaction furnishes a highly optically pure nitrobutylphenol intermediate, which is converted into an annulated tropone species by sequential oxidative dearomatization, conjugate addition, electrocyclic ring opening and nitrous acid elimination in the same reaction vessel. Both aliphatic and aromatic nitroalkenes are good substrates for the one-pot reaction, and this protocol appears to be general for various phenylpropionaldehydes as well. In the case of asymmetrically substituted phenylpropionaldehydes, the regioselectivity is likely determined by both the steric and electronic properties of the substituents. This methodology is successfully applied to the synthesis of the tricyclic core structure of Cephalotaxus norditerpenes.

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