Cas 1383545-61-6,4-[3,5-diacetoxy-7-(2-methylbut-3-en-2-yloxy)-4-oxo-4H-chromen-2-yl]-1,2-phenylene diacetate

1383545-61-6

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Basic information

Product Name: 4-[3,5-diacetoxy-7-(2-methylbut-3-en-2-yloxy)-4-oxo-4H-chromen-2-yl]-1,2-phenylene diacetate
Synonyms: 4-[3,5-diacetoxy-7-(2-methylbut-3-en-2-yloxy)-4-oxo-4H-chromen-2-yl]-1,2-phenylene diacetate
CAS NO:1383545-61-6
Molecular Formula:
Molecular Weight: 538.508
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: 4-[3,5-diacetoxy-7-(2-methylbut-3-en-2-yloxy)-4-oxo-4H-chromen-2-yl]-1,2-phenylene diacetate(CAS DataBase Reference)
NIST Chemistry Reference: 4-[3,5-diacetoxy-7-(2-methylbut-3-en-2-yloxy)-4-oxo-4H-chromen-2-yl]-1,2-phenylene diacetate(1383545-61-6)
EPA Substance Registry System: 4-[3,5-diacetoxy-7-(2-methylbut-3-en-2-yloxy)-4-oxo-4H-chromen-2-yl]-1,2-phenylene diacetate(1383545-61-6)

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: 1383545-61-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1383545-61-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,3,5,4 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1383545-61:
(9*1)+(8*3)+(7*8)+(6*3)+(5*5)+(4*4)+(3*5)+(2*6)+(1*1)=176
176 % 10 = 6
So 1383545-61-6 is a valid CAS Registry Number.

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1383545-61-6Relevant academic research and scientific papers

An efficient method for C8-prenylation of flavonols and flavanones

Kawamura, Tomoyuki,Hayashi, Moemi,Mukai, Rie,Terao, Junji,Nemoto, Hisao

, p. 1308 - 1314 (2012/06/30)

Synthesis of C8-prenylated flavonols and flavanones via the palladium-catalyzed 7-O-1,1-dimethylprop-2-enylation, followed by Claisen rearrangement is described. Two regioselectivities (carbon-carbon bond formation at either the tail or head of the prenyl

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