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(1S,2R)-2-fluorocyclohexanamine hydrochloride is a cyclic amine derivative with the molecular formula C6H13FClN. It features a fluorine substitution on the cyclohexane ring and is commonly used as the hydrochloride salt form in organic synthesis and pharmaceutical research. (1S,2R)-2-fluorocyclohexanamine hydrochloride's stereochemistry, with the 1S and 2R configuration, is crucial for its properties and potential biological activity, making it a promising candidate for drug discovery and development.

1335302-62-9

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1335302-62-9 Usage

Uses

Used in Pharmaceutical Research:
(1S,2R)-2-fluorocyclohexanamine hydrochloride is used as a building block in the synthesis of various pharmaceuticals and biologically active compounds. Its unique structure and functional groups contribute to the development of new drugs with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, (1S,2R)-2-fluorocyclohexanamine hydrochloride serves as an important intermediate for the creation of complex organic molecules. Its specific stereochemistry allows for the selective formation of desired products, which is valuable in the synthesis of enantiomerically pure compounds for medicinal and chemical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1335302-62-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,5,3,0 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1335302-62:
(9*1)+(8*3)+(7*3)+(6*5)+(5*3)+(4*0)+(3*2)+(2*6)+(1*2)=119
119 % 10 = 9
So 1335302-62-9 is a valid CAS Registry Number.

1335302-62-9Downstream Products

1335302-62-9Relevant academic research and scientific papers

Highly diastereoselective and general synthesis of primary β-fluoroamines

Schulte, Michael L.,Lindsley, Craig W.

supporting information; experimental part, p. 5684 - 5687 (2011/12/05)

A short, high yielding protocol has been developed for the highly diastereoselective (dr >20:1) and general synthesis of primary β-fluoroamines by the enantioselective α-fluorination of aldehydes, conversion into the N-sulfinyl aldimine, nucleophilic addi

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