Cas 909191-36-2,2-{(1E)-3-[(E)-1-phenylbut-2-enyloxy]prop-1-enyl}-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

909191-36-2

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Basic information

Product Name: 2-{(1E)-3-[(E)-1-phenylbut-2-enyloxy]prop-1-enyl}-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Synonyms: 2-{(1E)-3-[(E)-1-phenylbut-2-enyloxy]prop-1-enyl}-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS NO:909191-36-2
Molecular Formula:
Molecular Weight: 314.233
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-{(1E)-3-[(E)-1-phenylbut-2-enyloxy]prop-1-enyl}-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(CAS DataBase Reference)
NIST Chemistry Reference: 2-{(1E)-3-[(E)-1-phenylbut-2-enyloxy]prop-1-enyl}-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(909191-36-2)
EPA Substance Registry System: 2-{(1E)-3-[(E)-1-phenylbut-2-enyloxy]prop-1-enyl}-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(909191-36-2)

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: 909191-36-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 909191-36-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,9,1,9 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 909191-36:
(8*9)+(7*0)+(6*9)+(5*1)+(4*9)+(3*1)+(2*3)+(1*6)=182
182 % 10 = 2
So 909191-36-2 is a valid CAS Registry Number.

909191-36-2Upstream product

909191-36-2Downstream Products

909191-36-2Relevant academic research and scientific papers

Strategies for expanding structural diversity available from olefin isomerization-Claisen rearrangement reactions

Stevens, Benjamin D.,Bungard, Christopher J.,Nelson, Scott G.

, p. 6397 - 6402 (2007/10/03)

Boron-substituted di(allyl) ethers provide an efficient conduit for expanding the structural diversity available from olefin isomerization-Claisen rearrangement (ICR) reactions. Easily prepared allyl propargyl ethers undergo chemoselective Zr(IV)-catalyze

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