Cas 204917-29-3,sulfuric acid mono-{2-[3-(4-chloro-phenoxy)-2-hydroxy-propylamino]-ethyl} ester

204917-29-3

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Basic information

Product Name: sulfuric acid mono-{2-[3-(4-chloro-phenoxy)-2-hydroxy-propylamino]-ethyl} ester
Synonyms:
CAS NO:204917-29-3
Molecular Formula:
Molecular Weight: 325.77
EINECS: N/A
Product Categories: N/A
Mol File: 204917-29-3.mol
Article Data: 1

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: sulfuric acid mono-{2-[3-(4-chloro-phenoxy)-2-hydroxy-propylamino]-ethyl} ester(CAS DataBase Reference)
NIST Chemistry Reference: sulfuric acid mono-{2-[3-(4-chloro-phenoxy)-2-hydroxy-propylamino]-ethyl} ester(204917-29-3)
EPA Substance Registry System: sulfuric acid mono-{2-[3-(4-chloro-phenoxy)-2-hydroxy-propylamino]-ethyl} ester(204917-29-3)

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: 204917-29-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 204917-29-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,4,9,1 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 204917-29:
(8*2)+(7*0)+(6*4)+(5*9)+(4*1)+(3*7)+(2*2)+(1*9)=123
123 % 10 = 3
So 204917-29-3 is a valid CAS Registry Number.

204917-29-3Upstream product

204917-29-3Downstream Products

204917-29-3Relevant articles and documents

Binding of 2,4-substituted morpholines at human D4 dopamine receptors

Showell, Graham A.,Emms, Frances,Marwood, Rosemarie,O'Connor, Desmond,Patel, Smita,Leeson, Paul D.

, p. 1 - 8 (1998)

The synthesis of a series of 2,4-disubstituted morpholines is described and their affinities at human dopamine receptors reported. The orally bioavailable 7-azaindole compound 11 has nanomolar affinity at the hD4 receptor with > 1000-fold selectivity over the hD2 receptor.

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