Cas 1399383-29-9,ethyl 4-acetyl-2,3-dihydro-3-(4-methoxyphenyl)-5-methylfuran-2-carboxylate

1399383-29-9

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Basic information

Product Name: ethyl 4-acetyl-2,3-dihydro-3-(4-methoxyphenyl)-5-methylfuran-2-carboxylate
Synonyms:
CAS NO:1399383-29-9
Molecular Formula:
Molecular Weight: 304.343
EINECS: N/A
Product Categories: N/A
Mol File: 1399383-29-9.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: ethyl 4-acetyl-2,3-dihydro-3-(4-methoxyphenyl)-5-methylfuran-2-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 4-acetyl-2,3-dihydro-3-(4-methoxyphenyl)-5-methylfuran-2-carboxylate(1399383-29-9)
EPA Substance Registry System: ethyl 4-acetyl-2,3-dihydro-3-(4-methoxyphenyl)-5-methylfuran-2-carboxylate(1399383-29-9)

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: 1399383-29-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1399383-29-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,9,3,8 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1399383-29:
(9*1)+(8*3)+(7*9)+(6*9)+(5*3)+(4*8)+(3*3)+(2*2)+(1*9)=219
219 % 10 = 9
So 1399383-29-9 is a valid CAS Registry Number.

1399383-29-9Upstream product

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1399383-29-9Relevant articles and documents

The reactions of α-ylidene (vinylidene, benzylidene, styrylmethylidene) bis[carbonyls] with copper mono/bis[carbonylcarbenoids]

Merey, Goekce,Kaya, Mustafa,Anac, Olcay

experimental part, p. 1409 - 1424 (2012/10/07)

The [Cu(acac)2]-catalyzed reactions of various α,β,γ,δ-unsaturated bis-ketones/bis-esters/bis-keto esters with dimethyl diazomalonate and ethyl diazoacetate were studied. Total steric/electronic convenience of the present reaction paths was inv

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