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Methyl (2S,3S)-3-methyl-1-tosylpyrrolidine-2-carboxylate is a complex organic compound with the molecular formula C13H19NO4S. It is a chiral molecule, meaning it has a non-superimposable mirror image, and is characterized by its specific (2S,3S) configuration. methyl (2S,3S)-3-methyl-1-tosylpyrrolidine-2-carboxylate is a derivative of pyrrolidine, a five-membered cyclic amine, with a methyl group at the 3-position and a tosyl (tosylate) group at the 1-position. The tosyl group is a protecting group often used in organic synthesis to shield amine or hydroxyl groups from unwanted reactions. The carboxylate group is attached to the 2-position of the pyrrolidine ring, and the entire molecule is esterified with a methyl group. methyl (2S,3S)-3-methyl-1-tosylpyrrolidine-2-carboxylate is used as an intermediate in the synthesis of various pharmaceuticals and other organic compounds, taking advantage of its unique structural features and reactivity.

5846-10-6

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5846-10-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5846-10-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,4 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5846-10:
(6*5)+(5*8)+(4*4)+(3*6)+(2*1)+(1*0)=106
106 % 10 = 6
So 5846-10-6 is a valid CAS Registry Number.

5846-10-6Downstream Products

5846-10-6Relevant academic research and scientific papers

Copper-catalyzed remote (δ) C(sp3)-H bond amination: A practical strategy to construct pyrrolidine derivatives

Meng, Dongmei,Tang, Yongzhen,Wei, Junfa,Shi, Xianying,Yang, Mingyu

supporting information, p. 5744 - 5747 (2017/07/10)

We report a copper-catalyzed remote C(sp3)-H bond amination reaction that converts acyclic amines to pyrrolidines. This reaction occurs selectively at the carbon δ to the amine functionality. Primary, secondary and tertiary C-H bonds are all su

Visible-light-promoted remote C(sp3)-H amidation and chlorination

Qin, Qixue,Yu, Shouyun

, p. 1894 - 1897 (2015/04/27)

A visible-light-promoted C(sp3)-H amidation and chlorination of N-chlorosulfonamides (NCSs) is reported. This remote C(sp3)-H functionalization can be achieved in weak basic solution at room temperature with as little as 0.1 mol % of

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