Cas 98391-45-8,2,3-Naphthalenediol,5-[(2R)-3-[(1,1-dimethylethyl) amino]-2-hydroxypropoxy]-1,2,3,4-tetrahydro-,(2S,3R)-rel-

98391-45-8

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Basic information

Product Name: 2,3-Naphthalenediol,5-[(2R)-3-[(1,1-dimethylethyl) amino]-2-hydroxypropoxy]-1,2,3,4-tetrahydro-,(2S,3R)-rel-
Synonyms:
CAS NO:98391-45-8
Molecular Formula:
Molecular Weight: 309.406
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: 2,3-Naphthalenediol,5-[(2R)-3-[(1,1-dimethylethyl) amino]-2-hydroxypropoxy]-1,2,3,4-tetrahydro-,(2S,3R)-rel- (CAS DataBase Reference)
NIST Chemistry Reference: 2,3-Naphthalenediol,5-[(2R)-3-[(1,1-dimethylethyl) amino]-2-hydroxypropoxy]-1,2,3,4-tetrahydro-,(2S,3R)-rel- (98391-45-8)
EPA Substance Registry System: 2,3-Naphthalenediol,5-[(2R)-3-[(1,1-dimethylethyl) amino]-2-hydroxypropoxy]-1,2,3,4-tetrahydro-,(2S,3R)-rel- (98391-45-8)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 98391-45-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 98391-45-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,3,9 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 98391-45:
(7*9)+(6*8)+(5*3)+(4*9)+(3*1)+(2*4)+(1*5)=178
178 % 10 = 8
So 98391-45-8 is a valid CAS Registry Number.

98391-45-8Upstream product

98391-45-8Downstream Products

98391-45-8Relevant academic research and scientific papers

Nondepressant β-adrenergic blocking agents. I Substituted 3-amino-1-(5, 6, 7, 8-tetrahydro-1-naphthoxy)-2-propanols

Condon,Cimarusti,Fox,Narayanan,Reid,Sundeen,Hauck

, p. 913 - 922 (2007/10/06)

A series of 3-amino-1-(5,6,7,8-tetrahydronaphthoxy)-2-propanols was synthesized and investigated for β-adrenergic blocking activity and direct myocardial depressant action. The cis- and trans-diols 12-15 were found to retain the β-blocking potency of propranolol but to lack its myocardial depressant action. Compound 15 (nadolol) is currently undergoing extensive clinical evaluation as a potential antianginal, antiarrhythmic, and antihypertensive agent.

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