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(3-Chloro-4-cyclohexyl-phenyl)-methanol is a chemical compound with a molecular formula C13H16ClOH. It is a white to pale yellow solid that is primarily used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. (3-CHLORO-4-CYCLOHEXYL-PHENYL)-METHANOL contains a chloro, cyclohexyl, and phenyl group, making it useful in a variety of chemical reactions and applications. It is important for its potential medicinal and industrial uses and is typically handled and stored in accordance with standard safety protocols for handling organic compounds.

52758-47-1

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52758-47-1 Usage

Uses

Used in Pharmaceutical Industry:
(3-Chloro-4-cyclohexyl-phenyl)-methanol is used as an intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into various medicinal compounds.
Used in Organic Synthesis:
(3-Chloro-4-cyclohexyl-phenyl)-methanol is used as a building block in the synthesis of other organic compounds due to its unique structure and functional groups.

Check Digit Verification of cas no

The CAS Registry Mumber 52758-47-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,7,5 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 52758-47:
(7*5)+(6*2)+(5*7)+(4*5)+(3*8)+(2*4)+(1*7)=141
141 % 10 = 1
So 52758-47-1 is a valid CAS Registry Number.

52758-47-1Relevant academic research and scientific papers

HETEROARYLAMIDE LOWER CARBOXYLIC ACID DERIVATIVE

-

Page/Page column 225-226, (2009/02/10)

To provide a novel compound which has S1P receptor agonistic activity, exhibits excellent immunosuppressing effect, gives less adverse side effects, and can be orally administered. The invention provides a compound represented by general formula (I) (wherein A is a single bond, -O-, or - CH2-; R1 represents a hydrogen atom or a C1-C6 alkyl group, and V represents any one group selected from among the following groups (1) to (3) : (1) -G1-, (2) -G2-N(R2) -G3-, and (3) a group represented by formula 2, wherein each of Z1 and Z2 represents a hydrogen atom or a C1-C6 alkyl group, Z3 represents a hydrogen or the like, Q represents -CH2-O- or the like, and Y represents a group represented by foumula 3, a salt thereof, or a solvate thereof.

The preparation of immunosuppressant SR-31747

Burgess, Laurence E.

, p. 2181 - 2191 (2007/10/03)

The preparation of immunosuppressant SR-31747 is described. Attempts to install the Z-allyl amine included Lindlar partial hydrogenation and vinyl stannane methodologies. Ultimately, the Wittig olefination of aidehyde 12 with the ylide derived from β-amin

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