Cas 1037508-93-2,5-benzyloxy-2-(1,1-dimethylprop-2-en-1-yl)oxy-4-methyl-1-(1-methyl-1-hydroxybut-3-en-1-yl)benzene

1037508-93-2

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Basic information

Product Name: 5-benzyloxy-2-(1,1-dimethylprop-2-en-1-yl)oxy-4-methyl-1-(1-methyl-1-hydroxybut-3-en-1-yl)benzene
Synonyms: 5-benzyloxy-2-(1,1-dimethylprop-2-en-1-yl)oxy-4-methyl-1-(1-methyl-1-hydroxybut-3-en-1-yl)benzene
CAS NO:1037508-93-2
Molecular Formula:
Molecular Weight: 366.5
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: 5-benzyloxy-2-(1,1-dimethylprop-2-en-1-yl)oxy-4-methyl-1-(1-methyl-1-hydroxybut-3-en-1-yl)benzene(CAS DataBase Reference)
NIST Chemistry Reference: 5-benzyloxy-2-(1,1-dimethylprop-2-en-1-yl)oxy-4-methyl-1-(1-methyl-1-hydroxybut-3-en-1-yl)benzene(1037508-93-2)
EPA Substance Registry System: 5-benzyloxy-2-(1,1-dimethylprop-2-en-1-yl)oxy-4-methyl-1-(1-methyl-1-hydroxybut-3-en-1-yl)benzene(1037508-93-2)

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: 1037508-93-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1037508-93-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,7,5,0 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1037508-93:
(9*1)+(8*0)+(7*3)+(6*7)+(5*5)+(4*0)+(3*8)+(2*9)+(1*3)=142
142 % 10 = 2
So 1037508-93-2 is a valid CAS Registry Number.

1037508-93-2Upstream product

1037508-92-1 5-benzyloxy-4-methyl-2-(1,1-dimethylprop-2-yn-1-yl)oxy-1-(1-methyl-1-hydroxybut-3-en-1-yl)benzene

1037508-93-2Downstream Products

1037508-93-2Relevant academic research and scientific papers

A stereoselective route towards heliannuol A

Macías, Francisco A.,Chinchilla, David,Molinillo, Jose M.G.,Fronczek, Frank R.,Shishido, Kozo

, p. 5502 - 5508 (2008/09/21)

Both epimers of Heliannuol A, first heliannane reported in the literature, isolated from Heliannthus annuus, have been prepared individually in a stereoselective route using a ring closing metathesis (RCM) as a key step to obtain the eight-membered ring. Very good overall yield was obtained in both cases.

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