Cas 56255-41-5,1-(3-Cyclohexanesulfonyl-propylamino)-3-(2-nitro-phenoxy)-propan-2-ol

56255-41-5

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Basic information

Product Name: 1-(3-Cyclohexanesulfonyl-propylamino)-3-(2-nitro-phenoxy)-propan-2-ol
Synonyms:
CAS NO:56255-41-5
Molecular Formula:
Molecular Weight: 400.496
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1-(3-Cyclohexanesulfonyl-propylamino)-3-(2-nitro-phenoxy)-propan-2-ol(CAS DataBase Reference)
NIST Chemistry Reference: 1-(3-Cyclohexanesulfonyl-propylamino)-3-(2-nitro-phenoxy)-propan-2-ol(56255-41-5)
EPA Substance Registry System: 1-(3-Cyclohexanesulfonyl-propylamino)-3-(2-nitro-phenoxy)-propan-2-ol(56255-41-5)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 56255-41-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 56255-41-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,2,5 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 56255-41:
(7*5)+(6*6)+(5*2)+(4*5)+(3*5)+(2*4)+(1*1)=125
125 % 10 = 5
So 56255-41-5 is a valid CAS Registry Number.

56255-41-5Upstream product

21407-49-8 2-nitrophenyl glycidyl ether

56255-41-5Downstream Products

56255-41-5Relevant academic research and scientific papers

β-Adrenergic blocking agents. 18. 1-(Aryloxy)-3-(arylthioaklylamino)propan-2-ols and 1-substituted alkylthioamino-3-(aryloxy)propan-2-ols

Tucker,Coope

, p. 769 - 773 (2007/10/06)

The synthesis is described of a series of derivatives of 1-(aryloxy)-3-(arylthioalkylamino)propan-2-ols and 1-(alkylthioamino)- and 1-(aralkylamino)-3-(aryloxy)propan-2-ols. These compounds were investigated for their β-adrenoreceptor blocking properties and their selectivity of action for the cardiac β1 receptor. The structure-activity relationships are discussed with particular reference to the effects of the sulfur, sulfoxide, and sulfone groups on β-adrenoreceptor blocking potency and selectivity.

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