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1228560-90-4

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1228560-90-4 Usage

Description

(2R)-2-(4-CHLOROPHENYL)PYRROLIDINE HCL is a pyrrolidine derivative, a class of organic compounds, featuring a pyrrolidine ring with a 4-chlorophenyl group attached to it. The HCl in its name signifies that it is in the form of a hydrochloride salt, which is commonly used in pharmaceuticals to improve solubility and stability. The (2R) designation refers to the stereochemistry of the compound, indicating the specific orientation of the substituents around the pyrrolidine ring. Its uses and effects are determined by its pharmacological properties and interactions with biological systems.

Uses

Used in Pharmaceutical Industry:
(2R)-2-(4-CHLOROPHENYL)PYRROLIDINE HCL is used as a medication for the treatment of various medical conditions due to its specific pharmacological properties and interactions with biological systems. The exact applications and effects of this compound would depend on its ability to target and modulate specific biological pathways or receptors, providing therapeutic benefits for the treatment of the intended medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 1228560-90-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,8,5,6 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1228560-90:
(9*1)+(8*2)+(7*2)+(6*8)+(5*5)+(4*6)+(3*0)+(2*9)+(1*0)=154
154 % 10 = 4
So 1228560-90-4 is a valid CAS Registry Number.

1228560-90-4Upstream product

1228560-90-4Relevant articles and documents

Asymmetric synthesis of 2-arylpyrrolidines starting from γ-chloro N-(tert-butanesulfinyl)ketimines

Leemans, Erika,Mangelinckx, Sven,De Kimpe, Norbert

scheme or table, p. 3122 - 3124 (2010/09/04)

The enantioselective reductive cyclization of γ-chloro N-(tert-butanesulfinyl)ketimines towards the short and efficient synthesis of (S)- and (R)-2-arylpyrrolidines (ee >99%) is described for the first time by treatment with LiBEt3H and subsequ

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