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(5-cyclopropylfuran-2-yl)methanol is a chemical compound characterized by the presence of a cyclopropyl and furan ring in its structure, with a hydroxyl group attached to the furan ring. (5-cyclopropylfuran-2-yl)methanol is known for its unique structural properties, including the steric hindrance and rigidity imparted by the cyclopropyl group, which can significantly influence its biological activity. Its reactivity in organic reactions and potential as a building block make it a valuable component in the synthesis of various pharmaceuticals and agrochemicals.

1935403-22-7

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1935403-22-7 Usage

Uses

Used in Pharmaceutical Synthesis:
(5-cyclopropylfuran-2-yl)methanol is used as a key building block in the development of new pharmaceuticals. Its unique structural properties and reactivity in organic reactions allow for the creation of diverse and potentially effective drug candidates.
Used in Agrochemical Synthesis:
In the agrochemical industry, (5-cyclopropylfuran-2-yl)methanol is utilized as a starting material for the synthesis of novel agricultural products. Its structural properties and reactivity contribute to the development of innovative compounds with potential applications in pest control, crop protection, and other areas of agricultural science.
Used in Organic Synthesis:
(5-cyclopropylfuran-2-yl)methanol is employed as a versatile reactant in organic synthesis, where its cyclopropyl and furan ring structures, along with the hydroxyl group, enable the formation of a wide range of chemical products with various applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1935403-22-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,9,3,5,4,0 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1935403-22:
(9*1)+(8*9)+(7*3)+(6*5)+(5*4)+(4*0)+(3*3)+(2*2)+(1*2)=167
167 % 10 = 7
So 1935403-22-7 is a valid CAS Registry Number.

1935403-22-7Downstream Products

1935403-22-7Relevant academic research and scientific papers

The Influence of Substitution on Thiol-Induced Oxanorbornadiene Fragmentation

De Pascalis, Lucrezia,Yau, Mei-Kwan,Svatunek, Dennis,Tan, Zhuoting,Tekkam, Srinivas,Houk,Finn

, p. 3751 - 3754 (2021)

Oxanorbornadienes (ONDs) undergo facile Michael addition with thiols and then fragment by a retro-Diels-Alder (rDA) reaction, a unique two-step sequence among electrophilic cleavable linkages. The rDA reaction rate was explored as a function of the furan

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