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(3-fluorobicyclo[1.1.1]pentane-1-yl)methanol is a chemical compound that features a bicyclic structure with a fluorine atom attached to the carbon ring and a hydroxyl group attached to the carbon atom. (3-fluorobicyclo[1.1.1]pentane-1-yl)methanol is known for its unique properties due to the presence of the fluorine atom, which makes it a valuable building block in organic synthesis and medicinal chemistry for the development of pharmaceuticals and other bioactive molecules. The bicyclic structure further enhances its stability and chemical reactivity, contributing to its versatility in chemical research and development.

262852-01-7

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262852-01-7 Usage

Uses

Used in Pharmaceutical Industry:
(3-fluorobicyclo[1.1.1]pentane-1-yl)methanol is used as a building block for the synthesis of various pharmaceuticals, leveraging its unique properties and stability to create bioactive molecules with potential therapeutic applications.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (3-fluorobicyclo[1.1.1]pentane-1-yl)methanol serves as a key component in the development of new drugs, taking advantage of its fluorine atom and bicyclic structure to enhance the compound's reactivity and potential for diverse chemical interactions.
Used in Organic Synthesis:
(3-fluorobicyclo[1.1.1]pentane-1-yl)methanol is utilized as an intermediate in organic synthesis, where its unique properties and structural features contribute to the creation of a wide range of chemical compounds for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 262852-01-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,2,8,5 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 262852-01:
(8*2)+(7*6)+(6*2)+(5*8)+(4*5)+(3*2)+(2*0)+(1*1)=137
137 % 10 = 7
So 262852-01-7 is a valid CAS Registry Number.

262852-01-7Downstream Products

262852-01-7Relevant academic research and scientific papers

Large-Scale Synthesis and Modifications of Bicyclo[1.1.1]pentane-1,3-dicarboxylic Acid (BCP)

Ripenko, Vasyl,Vysochyn, Daniil,Klymov, Ivan,Zhersh, Serhii,Mykhailiuk, Pavel K.

, p. 14061 - 14068 (2021/07/20)

In flow photochemical addition of propellane to diacetyl allowed construction of the bicyclo[1.1.1]pentane (BCP) core in a 1 kg scale within 1 day. Haloform reaction of the formed diketone in batch afforded bicyclo[1.1.1]pentane-1,3-dicarboxylic acid in a

3-(5-METHOXY-1-OXOISOINDOLIN-2-YL)PIPERIDINE-2,6-DIONE DERIVATIVES AND USES THEREOF

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Page/Page column 271, (2021/06/26)

The present disclosure relates to compounds of formula (I') and pharmaceutical compositions and their use in reducing Widely Interspaced Zinc Finger Motifs (WIZ) expression levels, or inducing fetal hemoglobin (HbF) expression, and in the treatment of inherited blood disorders (e.g., hemoglobinopathies, e.g., beta-hemoglobinopathies), such as sickle cell disease and beta-thalassemia.

3-(5-HYDROXY-1-OXOISOINDOLIN-2-YL)PIPERIDINE-2,6-DIONE DERIVATIVES AND USES THEREOF

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Paragraph 1544-1545, (2020/02/05)

The present disclosure provides a compound of Formula (I′): or a pharmaceutically acceptable salt, hydrate, solvate, prodrug, stereoisomer, or tautomer thereof, wherein Rx, X1, X2, and R1 are as defined herein, and methods of making and using same.

Propeller alkane derivative, and preparation method, pharmaceutical composition and application thereof

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Page/Page column 17-18, (2020/09/16)

The invention provides a compound as shown in a general formula (I), a preparation method thereof, a pharmaceutical composition containing the compound and application of the compound as an AT2R regulator, wherein R1 is defined in the specification, and t

N-SUBSTITUTED TETRAHYDROTHIENOPYRIDINE DERIVATIVES AND USES THEREOF

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Paragraph 00154, (2020/01/11)

A compound of Formula (I) is provided that has been shown to be useful for treating a disease caused by a viral infection: (I) wherein R1, R2, R3, A, L, m, n, p and q are as defined herein.

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