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95656-79-4

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95656-79-4 Usage

Chemical structure

A derivative of 2-cyclopentylamino-ethanol with an amino group, a chloro group, and a cyano group attached to a phenyl ring.

Potential applications

In the field of medicinal chemistry.

Structural characteristics

The presence of an amino group, a chloro group, and a cyano group attached to a phenyl ring may contribute to its potential pharmacological activity.

Pharmacological activity

May have potential pharmacological activity due to its structural characteristics.

Drug candidate

Could be investigated for its potential as a drug candidate.

Research tool

May be used as a research tool in chemical biology and drug discovery.

Further studies

Additional research is needed to explore the potential uses and properties of this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 95656-79-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,6,5 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 95656-79:
(7*9)+(6*5)+(5*6)+(4*5)+(3*6)+(2*7)+(1*9)=184
184 % 10 = 4
So 95656-79-4 is a valid CAS Registry Number.

95656-79-4Downstream Products

95656-79-4Relevant articles and documents

Synthesis of further amino-halogen-substituted phenyl-aminoethanols

Kruger,Keck,Noll,Pieper

, p. 1612 - 1624 (2007/10/02)

Starting from clenbuterol as a lead structure, new 4-amino-phenyl-aminoethanol analogues have been synthesized by different approaches. In these compounds one or both of the chlorine atoms of clenbuterol are replaced by other residues. This has led to compounds with high intrinsic β2-mimetic and/or β1-blocking activities. 1-(4-Amino-3-chloro-5-trifluoromethyl-phenyl)-2-tert.-butylamino-ethanol hydrochloride (mabuterol) has been selected for clinical development. A detailed description is also given of the syntheses of new intermediate acetophenone derivatives as well as of the resolution of mabuterol into its enantiomers.

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