Cas 1370593-29-5,allyl 9-(4-tert-butylphenyl)-6-oxo-6H-benzo[c]chromene-8-carboxylate

1370593-29-5

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Basic information

Product Name: allyl 9-(4-tert-butylphenyl)-6-oxo-6H-benzo[c]chromene-8-carboxylate
Synonyms:
CAS NO:1370593-29-5
Molecular Formula:
Molecular Weight: 412.485
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: allyl 9-(4-tert-butylphenyl)-6-oxo-6H-benzo[c]chromene-8-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: allyl 9-(4-tert-butylphenyl)-6-oxo-6H-benzo[c]chromene-8-carboxylate(1370593-29-5)
EPA Substance Registry System: allyl 9-(4-tert-butylphenyl)-6-oxo-6H-benzo[c]chromene-8-carboxylate(1370593-29-5)

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: 1370593-29-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1370593-29-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,0,5,9 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1370593-29:
(9*1)+(8*3)+(7*7)+(6*0)+(5*5)+(4*9)+(3*3)+(2*2)+(1*9)=165
165 % 10 = 5
So 1370593-29-5 is a valid CAS Registry Number.

1370593-29-5Upstream product

1118-84-9 allyl acetoacetate

1370593-29-5Downstream Products

1370593-29-5Relevant academic research and scientific papers

One-pot synthesis of biaryl lactones by Sonogashira cross-coupling reactions of 4-chloro-3-formylcoumarin and subsequent domino [5+1] cyclization/deacetylation reactions with 1,3-dicarbonyl compounds

Iaroshenko, Viktor O.,Abbasi, Muhammad S. A.,Villinger, Alexander,Langer, Peter

, p. 803 - 806 (2012)

Biaryl lactones were prepared by a new palladium(0) and base-catalyzed one-pot reaction of 4-chloro-3-formylcoumarin with alkynes and 1,3-dicarbonyl compounds. Copyright

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