Cas 669087-52-9,Cyclopropanamine, 2-[2-[(tetrahydro-2H-pyran-2-yl)oxy]ethyl]-, (1R,2R)-rel- (9CI)

669087-52-9

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Basic information

Product Name: Cyclopropanamine, 2-[2-[(tetrahydro-2H-pyran-2-yl)oxy]ethyl]-, (1R,2R)-rel- (9CI)
Synonyms: Cyclopropanamine, 2-[2-[(tetrahydro-2H-pyran-2-yl)oxy]ethyl]-, (1R,2R)-rel- (9CI)
CAS NO:669087-52-9
Molecular Formula: C10H19NO2
Molecular Weight: 185.26
EINECS: N/A
Product Categories: METHOXY

Chemical Properties

Melting Point: N/A
Boiling Point: 276.4±25.0 °C(Predicted)
Flash Point: N/A
Appearance: /
Density: 1.06±0.1 g/cm3(Predicted)
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
PKA: 8.97±0.40(Predicted)
CAS DataBase Reference: Cyclopropanamine, 2-[2-[(tetrahydro-2H-pyran-2-yl)oxy]ethyl]-, (1R,2R)-rel- (9CI)(CAS DataBase Reference)
NIST Chemistry Reference: Cyclopropanamine, 2-[2-[(tetrahydro-2H-pyran-2-yl)oxy]ethyl]-, (1R,2R)-rel- (9CI)(669087-52-9)
EPA Substance Registry System: Cyclopropanamine, 2-[2-[(tetrahydro-2H-pyran-2-yl)oxy]ethyl]-, (1R,2R)-rel- (9CI)(669087-52-9)

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: 669087-52-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 669087-52-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,9,0,8 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 669087-52:
(8*6)+(7*6)+(6*9)+(5*0)+(4*8)+(3*7)+(2*5)+(1*2)=209
209 % 10 = 9
So 669087-52-9 is a valid CAS Registry Number.

669087-52-9Upstream product

669087-52-9Downstream Products

669087-52-9Relevant academic research and scientific papers

Synthesis of cyclopropanoid nucleoside analogues possessing a flexible side chain

Csuk, René,Kern, Anja

, p. 843 - 852 (2003)

A novel class of cyclopropanoic nucleoside analogues containing an hydroxyethyl residue instead of a hydroxymethyl side chain has been prepared in an easy sequence. These compounds showed weak antitumor activity. The resolution of the racemates on an analytical scale was performed by HPLC using chiral stationary phases.

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