39075-78-0 Usage
Description
St 2075, also known as (2,6-Dichloro-phenyl)guanidine, is an impurity of Clonidine (C587132). It is an α2-Adrenergic agonist with potential applications in the medical field due to its various pharmacological properties.
Uses
Used in Pharmaceutical Industry:
St 2075 is used as an α2-Adrenergic agonist for its ability to interact with adrenergic receptors, which can have various therapeutic effects.
Used in Antihypertensive Applications:
St 2075 is used as an antihypertensive agent to help lower blood pressure. Its agonistic action on α2-adrenergic receptors can lead to vasodilation and a reduction in blood pressure.
Used in Analgesic Applications:
St 2075 is used as an analgesic for neuropathic pain, providing relief from pain caused by nerve damage or dysfunction. Its agonistic properties on adrenergic receptors may contribute to its pain-relieving effects.
Check Digit Verification of cas no
The CAS Registry Mumber 39075-78-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,0,7 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 39075-78:
(7*3)+(6*9)+(5*0)+(4*7)+(3*5)+(2*7)+(1*8)=140
140 % 10 = 0
So 39075-78-0 is a valid CAS Registry Number.
39075-78-0Relevant articles and documents
THERAPEUTIC COMPOUNDS
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Paragraph 0461; 0462, (2018/08/30)
The invention provides compounds of formula Ia′, Ib′, Ic′, and Id′: and pharmaceutically acceptable salts thereof, wherein the variables A, R6, R7, R8, R9, Rx, L, X, Y, and Z have the meaning as described herein. The compounds are useful for reducing endoplasmic reticulum stress and for producing analgesia in an animal.
A traceless linker approach to the solid phase synthesis of substituted guanidines utilizing a novel acyl isothiocyanate resin
Wilson, Lawrence J.,Klopfenstein, Sean R.,Li, Min
, p. 3999 - 4002 (2007/10/03)
Solid phase synthesis of a series of substituted guanidines based on a novel acyl isothiocyanate resin is presented. This method provides both mono and disubstituted guanidines with a variety of sterically demanding and/or electron withdrawing substituents in good purities and yields.
