Cas 169776-17-4,allyl 3-<4',5'-dimethoxy-2'-(methoxymethoxy)phenyl>-4-oxochromane-3-carboxylate

169776-17-4

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Basic information

Product Name: allyl 3-<4',5'-dimethoxy-2'-(methoxymethoxy)phenyl>-4-oxochromane-3-carboxylate
Synonyms: allyl 3-<4',5'-dimethoxy-2'-(methoxymethoxy)phenyl>-4-oxochromane-3-carboxylate
CAS NO:169776-17-4
Molecular Formula:
Molecular Weight: 428.439
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 3-<4',5'-dimethoxy-2'-(methoxymethoxy)phenyl>-4-oxochromane-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: allyl 3-<4',5'-dimethoxy-2'-(methoxymethoxy)phenyl>-4-oxochromane-3-carboxylate(169776-17-4)
EPA Substance Registry System: allyl 3-<4',5'-dimethoxy-2'-(methoxymethoxy)phenyl>-4-oxochromane-3-carboxylate(169776-17-4)

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: 169776-17-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 169776-17-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,7,7 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 169776-17:
(8*1)+(7*6)+(6*9)+(5*7)+(4*7)+(3*6)+(2*1)+(1*7)=194
194 % 10 = 4
So 169776-17-4 is a valid CAS Registry Number.

169776-17-4Upstream product

153488-86-9 3-(allyloxycarbonyl)chroman-4-one

169776-17-4Downstream Products

169776-17-4Relevant academic research and scientific papers

Organolead-mediated arylation of allyl β-keto esters: selective synthesis of 2'-hydroxyisoflavones

Donnelly, Dervilla M. X.,Finet, Jean-Pierre,Rattigan, Bernard A.

, p. 1679 - 1684 (2007/10/02)

Arylation of the A-ring-unsubstituted and -substituted 3-(allyloxycarbonyl)chroman-4-ones 6-8 with lead(IV) triacetate 5 followed by selective catalytic deallyloxycarbonylation-dehydrogenation afforded 2'-protected

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