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(1-(o-tolyl)cyclopropyl)methanol, also known as o-Phenylcyclopropylmethanol, is a cyclopropyl derivative featuring a methanol group attached to a cyclopropyl ring that is substituted with an o-tolyl group. (1-(o-tolyl)cyclopropyl)methanol is distinguished by its unique three-membered cyclopropyl ring, which endows it with heightened reactivity and makes it a valuable asset in organic synthesis.

886366-30-9

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886366-30-9 Usage

Uses

Used in Pharmaceutical Industry:
(1-(o-tolyl)cyclopropyl)methanol serves as a synthetic intermediate in the production of various pharmaceuticals. Its reactivity and structural features make it instrumental in the synthesis of complex organic molecules and drug candidates, contributing to the development of new medications.
Used in Agrochemical Industry:
In the agrochemical sector, (1-(o-tolyl)cyclopropyl)methanol is similarly utilized as a synthetic intermediate. Its role in creating agrochemicals is crucial for the production of effective and innovative products designed to protect crops and enhance agricultural yields.
Used in Organic Synthesis:
(1-(o-tolyl)cyclopropyl)methanol is employed as a building block in organic synthesis. Its unique cyclopropyl ring allows for the creation of a wide range of organic molecules, making it an essential component in the advancement of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 886366-30-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,3,6 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 886366-30:
(8*8)+(7*8)+(6*6)+(5*3)+(4*6)+(3*6)+(2*3)+(1*0)=219
219 % 10 = 9
So 886366-30-9 is a valid CAS Registry Number.

886366-30-9Downstream Products

886366-30-9Relevant academic research and scientific papers

Rhodium-Catalyzed Enantioselective Silylation of Cyclopropyl C?H Bonds

Lee, Taegyo,Hartwig, John F.

supporting information, p. 8723 - 8727 (2016/07/21)

Hydrosilyl ethers, generated in situ by the dehydrogenative silylation of cyclopropylmethanols with diethylsilane, undergo asymmetric, intramolecular silylation of cyclopropyl C?H bonds in high yields and with high enantiomeric excesses in the presence of

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