Cas 1444827-09-1,(Z)-4,4,5,5-tetramethyl-2-[3-(4-trifluoromethylphenyl)prop-1-enyl]-[1,3,2]-dioxaborolane

1444827-09-1

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Basic information

Product Name: (Z)-4,4,5,5-tetramethyl-2-[3-(4-trifluoromethylphenyl)prop-1-enyl]-[1,3,2]-dioxaborolane
Synonyms:
CAS NO:1444827-09-1
Molecular Formula:
Molecular Weight: 312.14
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: (Z)-4,4,5,5-tetramethyl-2-[3-(4-trifluoromethylphenyl)prop-1-enyl]-[1,3,2]-dioxaborolane(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-4,4,5,5-tetramethyl-2-[3-(4-trifluoromethylphenyl)prop-1-enyl]-[1,3,2]-dioxaborolane(1444827-09-1)
EPA Substance Registry System: (Z)-4,4,5,5-tetramethyl-2-[3-(4-trifluoromethylphenyl)prop-1-enyl]-[1,3,2]-dioxaborolane(1444827-09-1)

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: 1444827-09-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1444827-09-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,4,8,2 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1444827-09:
(9*1)+(8*4)+(7*4)+(6*4)+(5*8)+(4*2)+(3*7)+(2*0)+(1*9)=171
171 % 10 = 1
So 1444827-09-1 is a valid CAS Registry Number.

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1444827-09-1Relevant academic research and scientific papers

Synthesis of alkenyl boronates from allyl-substituted aromatics using an olefin cross-metathesis protocol

Hemelaere, Remy,Carreaux, Francois,Carboni, Bertrand

, p. 6786 - 6792 (2013/07/26)

An efficient synthesis of 3-aryl-1-propenyl boronates from pinacol vinyl boronic ester and allyl-substituted aromatics by cross metathesis is reported. Although the allylbenzene derivatives are prone to isomerization reaction under metathesis conditions,

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