54280-77-2 Usage
Uses
Used in Pharmaceutical Industry:
2-(Cyclopropylmethoxy)benzaldehyde is utilized as an intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the creation of a wide array of medicinal compounds, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(cyclopropylmethoxy)benzaldehyde serves as a key component in the production of different agrochemicals. Its incorporation into these products can enhance their effectiveness in agricultural applications, such as pest control and crop protection.
Used in Perfume Industry:
2-(Cyclopropylmethoxy)benzaldehyde is employed as a fragrance ingredient in the perfume industry. Its aromatic properties make it a desirable component in the creation of various scents, adding depth and complexity to perfume compositions.
Used in Organic Synthesis:
2-(Cyclopropylmethoxy)benzaldehyde is a versatile compound in organic synthesis, with potential applications across a broad spectrum of chemical reactions. Its reactivity and structural features make it a valuable building block for the synthesis of complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 54280-77-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,2,8 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54280-77:
(7*5)+(6*4)+(5*2)+(4*8)+(3*0)+(2*7)+(1*7)=122
122 % 10 = 2
So 54280-77-2 is a valid CAS Registry Number.
54280-77-2Relevant academic research and scientific papers
CYANO SUBSTITUTED HETEROARYLPYRIMIDINONE DERIVATIVE, PREPARATION METHOD AND USE THEREOF
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Paragraph 0238-0240, (2020/04/24)
The present invention relates to a cyano-substituted heteroarylpyrimidinone derivative represented by formula (I), a preparation method therefor and a use thereof as a therapeutic agent, in particular a use as an acetyl-CoA carboxylase (ACC) inhibitor, an
Iron-catalyzed oxidative C-C(vinyl) σ-bond cleavage of allylarenes to aryl aldehydes at room temperature with ambient air
Liu, Binbin,Cheng, Lu,Hu, Penghui,Xu, Fangning,Li, Dan,Gu, Wei-Jin,Han, Wei
, p. 4817 - 4820 (2019/05/02)
A general and selective iron-catalyzed allylic C-C(vinyl) σ-bond cleavage of allylarenes without the assistance of heteroatoms to give aryl aldehydes is reported. The unstrained carbon-carbon single bond cleavage reaction uses ambient air as the sole oxidant, proceeds efficiently at room temperature, and allows for exceptional functional-group tolerance, which addresses the long-standing challenges of current C-C bond cleavage/functionalization. Notably, the method enables rapid late-stage oxidation of complex bioactive molecules and can be used to expedite syntheses of natural products (vanillin and glucovanillin) from readily available chemical feedstocks.
