Cas 1381932-54-2,ethyl 2-(4-oxo-3-(3,4,5-trimethoxyphenyl)-4,5,6,7-tetrahydrobenzofuran-2-yl)acetate

1381932-54-2

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Basic information

Product Name: ethyl 2-(4-oxo-3-(3,4,5-trimethoxyphenyl)-4,5,6,7-tetrahydrobenzofuran-2-yl)acetate
Synonyms: ethyl 2-(4-oxo-3-(3,4,5-trimethoxyphenyl)-4,5,6,7-tetrahydrobenzofuran-2-yl)acetate
CAS NO:1381932-54-2
Molecular Formula:
Molecular Weight: 388.417
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: ethyl 2-(4-oxo-3-(3,4,5-trimethoxyphenyl)-4,5,6,7-tetrahydrobenzofuran-2-yl)acetate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 2-(4-oxo-3-(3,4,5-trimethoxyphenyl)-4,5,6,7-tetrahydrobenzofuran-2-yl)acetate(1381932-54-2)
EPA Substance Registry System: ethyl 2-(4-oxo-3-(3,4,5-trimethoxyphenyl)-4,5,6,7-tetrahydrobenzofuran-2-yl)acetate(1381932-54-2)

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: 1381932-54-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1381932-54-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,1,9,3 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1381932-54:
(9*1)+(8*3)+(7*8)+(6*1)+(5*9)+(4*3)+(3*2)+(2*5)+(1*4)=172
172 % 10 = 2
So 1381932-54-2 is a valid CAS Registry Number.

1381932-54-2Upstream product

1381932-54-2Downstream Products

1381932-54-2Relevant academic research and scientific papers

Synthesis of functionalized and fused furans and pyrans from the Morita-Baylis-Hillman acetates of nitroalkenes

Nair, Divya K.,Mobin, Shaikh M.,Namboothiri, Irishi N.N.

supporting information; experimental part, p. 3349 - 3352 (2012/07/28)

The Morita-Baylis-Hillman (MBH) acetates derived from nitroalkenes and ethyl glyoxylate have been transformed in one pot at room temperature to highly fused and functionalized furans and pyrans in good to excellent yield. The reaction involves a cascade M

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