Cas 1415029-17-2,ethyl 4-(2-((1-(3-fluorobenzyl)-1H-1,2,3-triazol-4-yl)methoxy)-5-bromophenyl)-2-amino-5,6,7,8-tetrahydro-7,7-dimethyl-5-oxo-4H-chromene-3-carboxylate

1415029-17-2

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Basic information

Product Name: ethyl 4-(2-((1-(3-fluorobenzyl)-1H-1,2,3-triazol-4-yl)methoxy)-5-bromophenyl)-2-amino-5,6,7,8-tetrahydro-7,7-dimethyl-5-oxo-4H-chromene-3-carboxylate
Synonyms:
CAS NO:1415029-17-2
Molecular Formula:
Molecular Weight: 625.494
EINECS: N/A
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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-(2-((1-(3-fluorobenzyl)-1H-1,2,3-triazol-4-yl)methoxy)-5-bromophenyl)-2-amino-5,6,7,8-tetrahydro-7,7-dimethyl-5-oxo-4H-chromene-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 4-(2-((1-(3-fluorobenzyl)-1H-1,2,3-triazol-4-yl)methoxy)-5-bromophenyl)-2-amino-5,6,7,8-tetrahydro-7,7-dimethyl-5-oxo-4H-chromene-3-carboxylate(1415029-17-2)
EPA Substance Registry System: ethyl 4-(2-((1-(3-fluorobenzyl)-1H-1,2,3-triazol-4-yl)methoxy)-5-bromophenyl)-2-amino-5,6,7,8-tetrahydro-7,7-dimethyl-5-oxo-4H-chromene-3-carboxylate(1415029-17-2)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1415029-17-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1415029-17-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,0,2 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1415029-17:
(9*1)+(8*4)+(7*1)+(6*5)+(5*0)+(4*2)+(3*9)+(2*1)+(1*7)=122
122 % 10 = 2
So 1415029-17-2 is a valid CAS Registry Number.

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1415029-17-2Relevant academic research and scientific papers

Efficient one-pot, four-component synthesis of 1,2,3-triazole-linked tetrahydrobenzo[ b[pyrans

MaGee, David I.,Salehi, Peyman,Dabiri, Minoo,Bahramnejad, Mahboobeh

, p. 486 - 497 (2013/01/15)

A one-pot procedure has been developed for the synthesis of (1,2,3-triazolyl) methoxyphenyl tetrahydro-5-oxo-4H-chromene derivatives by concurrent reaction of aryloxy propargylated aldehydes, various azides, active methylene compounds, and 1,3-cyclohexanediones using catalytic amounts of Cu(OAc) 2/sodium ascorbate and diammonium hydrogen phosphate in aqueous ethanol media. Excellent conversion of starting materials was achieved to the desired (1,2,3-triazolyl) methoxyphenyl tetrahydro-5-oxo-4H-chromene products.

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