Cas 849612-27-7,Propanoic acid, 3-[[(2Z)-4-(acetyloxy)-2-butenyl][(4-methoxyphenyl)methyl]amino]-3-oxo- , methyl ester

849612-27-7

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Basic information

Product Name: Propanoic acid, 3-[[(2Z)-4-(acetyloxy)-2-butenyl][(4-methoxyphenyl)methyl]amino]-3-oxo- , methyl ester
Synonyms:
CAS NO:849612-27-7
Molecular Formula: C18H23NO6
Molecular Weight: 349.384
EINECS: N/A
Product Categories: N/A
Mol File: 849612-27-7.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: Propanoic acid, 3-[[(2Z)-4-(acetyloxy)-2-butenyl][(4-methoxyphenyl)methyl]amino]-3-oxo- , methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Propanoic acid, 3-[[(2Z)-4-(acetyloxy)-2-butenyl][(4-methoxyphenyl)methyl]amino]-3-oxo- , methyl ester(849612-27-7)
EPA Substance Registry System: Propanoic acid, 3-[[(2Z)-4-(acetyloxy)-2-butenyl][(4-methoxyphenyl)methyl]amino]-3-oxo- , methyl ester(849612-27-7)

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: 849612-27-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 849612-27-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,6,1 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 849612-27:
(8*8)+(7*4)+(6*9)+(5*6)+(4*1)+(3*2)+(2*2)+(1*7)=197
197 % 10 = 7
So 849612-27-7 is a valid CAS Registry Number.

849612-27-7Upstream product

849612-27-7Downstream Products

849612-27-7Relevant articles and documents

Surprisingly mild "enolate-counterion-free" Pd(0)-catalyzed intramolecular allylic alkylations

Madec, David,Prestat, Guillaume,Martini, Elisabetta,Fristrup, Peter,Poli, Giovanni,Norrby, Per-Ola

, p. 995 - 998 (2005)

(Chemical Equation Presented) Palladium-catalyzed intramolecular allylic alkylations of unsaturated EWG-activated amides can take place under phase-transfer conditions or in the presence of a crown ether. These new reaction conditions are milder and highe

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