Cas 93767-24-9,2-Propen-1-one, 1-[2-hydroxy-4,6-bis(methoxymethoxy)phenyl]-3-[4-(methoxymethoxy)-3- (3-methyl-2-butenyl)phenyl]-, (E)-

93767-24-9

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Basic information

Product Name: 2-Propen-1-one, 1-[2-hydroxy-4,6-bis(methoxymethoxy)phenyl]-3-[4-(methoxymethoxy)-3- (3-methyl-2-butenyl)phenyl]-, (E)-
Synonyms:
CAS NO:93767-24-9
Molecular Formula: C26H32O8
Molecular Weight: 472.535
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: 2-Propen-1-one, 1-[2-hydroxy-4,6-bis(methoxymethoxy)phenyl]-3-[4-(methoxymethoxy)-3- (3-methyl-2-butenyl)phenyl]-, (E)-(CAS DataBase Reference)
NIST Chemistry Reference: 2-Propen-1-one, 1-[2-hydroxy-4,6-bis(methoxymethoxy)phenyl]-3-[4-(methoxymethoxy)-3- (3-methyl-2-butenyl)phenyl]-, (E)-(93767-24-9)
EPA Substance Registry System: 2-Propen-1-one, 1-[2-hydroxy-4,6-bis(methoxymethoxy)phenyl]-3-[4-(methoxymethoxy)-3- (3-methyl-2-butenyl)phenyl]-, (E)-(93767-24-9)

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: 93767-24-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 93767-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,7,6 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 93767-24:
(7*9)+(6*3)+(5*7)+(4*6)+(3*7)+(2*2)+(1*4)=169
169 % 10 = 9
So 93767-24-9 is a valid CAS Registry Number.

93767-24-9Upstream product

93767-24-9Downstream Products

93767-24-9Relevant academic research and scientific papers

Synthesis of Euchrestaflavanone-A

Khan, Saeed Ahmad,Krishnamurti, M.

, p. 887 - 888 (2007/10/02)

The reaction of 2-methyl-but-3-en-2-ol with 5,7,4'-trihydroxy-3'-prenylflavanone (III) gives 5,7,4'-trihydroxy-3,6-diprenylflavanone (IV)(euchrestaflavanone-A), its monochroman (V) and a dichroman (VI).The flavanone III in turn has been prepared by the condensation of 6-hydroxy-2,4-dimethoxymethoxyacetophenone and 4-methoxymethoxy-3-prenylbanzaldehyde followed by cyclization and demethoxymethylation.

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