Cas 129333-19-3,Acetic acid 3-acetoxy-5-[2-(1,1-dimethoxy-ethyl)-piperidine-1-carbonyl]-phenyl ester

129333-19-3

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Basic information

Product Name: Acetic acid 3-acetoxy-5-[2-(1,1-dimethoxy-ethyl)-piperidine-1-carbonyl]-phenyl ester
Synonyms:
CAS NO:129333-19-3
Molecular Formula:
Molecular Weight: 393.437
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: Acetic acid 3-acetoxy-5-[2-(1,1-dimethoxy-ethyl)-piperidine-1-carbonyl]-phenyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid 3-acetoxy-5-[2-(1,1-dimethoxy-ethyl)-piperidine-1-carbonyl]-phenyl ester(129333-19-3)
EPA Substance Registry System: Acetic acid 3-acetoxy-5-[2-(1,1-dimethoxy-ethyl)-piperidine-1-carbonyl]-phenyl ester(129333-19-3)

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: 129333-19-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 129333-19-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,3,3 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 129333-19:
(8*1)+(7*2)+(6*9)+(5*3)+(4*3)+(3*3)+(2*1)+(1*9)=123
123 % 10 = 3
So 129333-19-3 is a valid CAS Registry Number.

129333-19-3Upstream product

129333-19-3Downstream Products

128033-72-7 2-acetyl-1-<3,5-bis(acetyloxy)benzoyl>-piperidine

129333-19-3Relevant academic research and scientific papers

BASE-INDUCED CONDENSATION OF PHENOLS JOINED BY AMIDES TO KETONES: A SYNTHESIS OF HYDROXYLATED ISOQUINOLINONES AND DERIVATIVES

Friary, Richard,Schwerdt, John H.,Seidl, Vera,Topliss, John G.

, p. 419 - 422 (2007/10/02)

Potassium carbonate in methanol saponified the acetate ester groups of certain meta-acetoxylated α-benzamido ketones and cyclized the resulting phenols in situ to give a series of hydroxylated isoquinolinones and derivatives.

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