Cas 127376-12-9,{2-[2-(4-Methoxy-2-oxo-cyclohex-3-enyl)-ethyl]-[1,3]dioxolan-2-yl}-acetic acid methyl ester

127376-12-9

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Basic information

Product Name: {2-[2-(4-Methoxy-2-oxo-cyclohex-3-enyl)-ethyl]-[1,3]dioxolan-2-yl}-acetic acid methyl ester
Synonyms: {2-[2-(4-Methoxy-2-oxo-cyclohex-3-enyl)-ethyl]-[1,3]dioxolan-2-yl}-acetic acid methyl ester
CAS NO:127376-12-9
Molecular Formula:
Molecular Weight: 298.336
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: {2-[2-(4-Methoxy-2-oxo-cyclohex-3-enyl)-ethyl]-[1,3]dioxolan-2-yl}-acetic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: {2-[2-(4-Methoxy-2-oxo-cyclohex-3-enyl)-ethyl]-[1,3]dioxolan-2-yl}-acetic acid methyl ester(127376-12-9)
EPA Substance Registry System: {2-[2-(4-Methoxy-2-oxo-cyclohex-3-enyl)-ethyl]-[1,3]dioxolan-2-yl}-acetic acid methyl ester(127376-12-9)

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: 127376-12-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 127376-12-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,3,7 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 127376-12:
(8*1)+(7*2)+(6*7)+(5*3)+(4*7)+(3*6)+(2*1)+(1*2)=129
129 % 10 = 9
So 127376-12-9 is a valid CAS Registry Number.

127376-12-9Upstream product

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127376-12-9Relevant academic research and scientific papers

ENOLIC ORTHO ESTERS. V. REGIOSPECIFIC GENERATION OF DIKETO ESTER MONOACETALS BY REACTION OF AN ENOLIC ORTHO ESTER WITH KETENE SILYL ACETALS.

Collins, D. J.,Dosen, M.,Jhingran, A. G.

, p. 421 - 422 (2007/10/02)

Reaction of the enolic ortho ester (1) with the ketene silyl acetals (2a-c) in dichloromethane in the presence of titanium tetrachloride at low temperatures gave the respective keto acetal esters (6a-c) via the titanium enolates (3a-c).

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