Cas 30392-69-9,3-(isovaleryloxymethyl)-4-(isovaleryloxy)phenyl tert-butylaminomethyl ketone methanesulfonate

30392-69-9

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Basic information

Product Name: 3-(isovaleryloxymethyl)-4-(isovaleryloxy)phenyl tert-butylaminomethyl ketone methanesulfonate
Synonyms: 3-(isovaleryloxymethyl)-4-(isovaleryloxy)phenyl tert-butylaminomethyl ketone methanesulfonate
CAS NO:30392-69-9
Molecular Formula:
Molecular Weight: 501.642
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: 3-(isovaleryloxymethyl)-4-(isovaleryloxy)phenyl tert-butylaminomethyl ketone methanesulfonate(CAS DataBase Reference)
NIST Chemistry Reference: 3-(isovaleryloxymethyl)-4-(isovaleryloxy)phenyl tert-butylaminomethyl ketone methanesulfonate(30392-69-9)
EPA Substance Registry System: 3-(isovaleryloxymethyl)-4-(isovaleryloxy)phenyl tert-butylaminomethyl ketone methanesulfonate(30392-69-9)

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: 30392-69-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 30392-69-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,3,9 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 30392-69:
(7*3)+(6*0)+(5*3)+(4*9)+(3*2)+(2*6)+(1*9)=99
99 % 10 = 9
So 30392-69-9 is a valid CAS Registry Number.

30392-69-9Upstream product

30392-69-9Downstream Products

47633-81-8 3-Methyl-butyric acid 4-(2-tert-butylamino-1-hydroxy-ethyl)-2-(3-methyl-butyryloxymethyl)-phenyl ester

30392-69-9Relevant academic research and scientific papers

Esters of 3-(hydroxy or hydroxymethyl)-4-hydroxyphenyl aminomethyl ketones

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, (2008/06/13)

Mono-, di- and tri-esters of 3-(hydroxy or hydroxymethyl)-4-hydroxy-alpha-(aminomethyl)benzyl alcohols, obtained by methods involving reduction of the corresponding mono- and di-ester ketones, are useful for producing sympathomimetic effects, such as bronchodilation, of long duration with low cardiovascular stimulating effect, in warm-blooded mammals.

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