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10479-74-0

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10479-74-0 Usage

Description

((1S,2R)-2-Chloromethyl-cyclohexyl)-methanol is a chiral chemical compound with the molecular formula C8H15ClO. It possesses two stereoisomers, (1S,2R) and (1R,2S), and is primarily utilized in organic synthesis and pharmaceutical research.

Uses

Used in Pharmaceutical Research:
((1S,2R)-2-Chloromethyl-cyclohexyl)-methanol is used as a building block for the synthesis of various pharmaceutical intermediates and active ingredients. Its unique structure and chirality make it a valuable component in the development of new drugs and bioactive molecules.
Used in Organic Synthesis:
((1S,2R)-2-Chloromethyl-cyclohexyl)-methanol is used as a reagent in the preparation of chiral compounds for use in medicinal chemistry. Its versatility in organic synthesis allows for the creation of a wide range of pharmaceutically relevant compounds.
Used in Drug Development:
((1S,2R)-2-Chloromethyl-cyclohexyl)-methanol has potential applications in the development of new drugs and bioactive molecules, contributing to the advancement of pharmaceutical research and the discovery of innovative treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 10479-74-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,7 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10479-74:
(7*1)+(6*0)+(5*4)+(4*7)+(3*9)+(2*7)+(1*4)=100
100 % 10 = 0
So 10479-74-0 is a valid CAS Registry Number.

10479-74-0Downstream Products

10479-74-0Relevant articles and documents

Sequenced Reactions with Samarium(II) Iodide. Sequential Intermolecular Carbonyl Addition/Intramolecular Nucleophilic Acyl Substitution for the Preparation of Seven-, Eight-, and Nine-Membered Carbocycles

Molander, Gary A.,Alonso-Alija, Cristina

, p. 4366 - 4373 (2007/10/03)

Samarium(II) iodide has been employed to promote a tandem intermolecular carbonyl addition/ intramolecular nucleophilic acyl substitution sequence, generating seven-through nine-membered monocyclic, bicyclic, and tricyclic ring systems with good yields an

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