Cas 30392-72-4,Propanoic acid, 2,2-dimethyl-, 4-[2-[(1,1-dimethylethyl)amino]-1-hydroxyethyl]-1,2-phenylene ester, hydrochloride

30392-72-4

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Basic information

Product Name: Propanoic acid, 2,2-dimethyl-, 4-[2-[(1,1-dimethylethyl)amino]-1-hydroxyethyl]-1,2-phenylene ester, hydrochloride
Synonyms:
CAS NO:30392-72-4
Molecular Formula: C22H35NO5.ClH
Molecular Weight: 429.985
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: Propanoic acid, 2,2-dimethyl-, 4-[2-[(1,1-dimethylethyl)amino]-1-hydroxyethyl]-1,2-phenylene ester, hydrochloride(CAS DataBase Reference)
NIST Chemistry Reference: Propanoic acid, 2,2-dimethyl-, 4-[2-[(1,1-dimethylethyl)amino]-1-hydroxyethyl]-1,2-phenylene ester, hydrochloride(30392-72-4)
EPA Substance Registry System: Propanoic acid, 2,2-dimethyl-, 4-[2-[(1,1-dimethylethyl)amino]-1-hydroxyethyl]-1,2-phenylene ester, hydrochloride(30392-72-4)

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: 30392-72-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 30392-72-4 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, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 30392-72:
(7*3)+(6*0)+(5*3)+(4*9)+(3*2)+(2*7)+(1*2)=94
94 % 10 = 4
So 30392-72-4 is a valid CAS Registry Number.

30392-72-4Upstream product

30415-88-4 3,4-bis-(pivalyloxy)phenyl tert-butylaminomethyl ketone hydrochloride

30392-72-4Downstream Products

30392-72-4Relevant 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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