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Boronic acid, (3-phenyl-1-propenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

214907-30-9

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214907-30-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 214907-30-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,9,0 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 214907-30:
(8*2)+(7*1)+(6*4)+(5*9)+(4*0)+(3*7)+(2*3)+(1*0)=119
119 % 10 = 9
So 214907-30-9 is a valid CAS Registry Number.

214907-30-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-3-phenylprop-1-enylboronic acid

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:214907-30-9 SDS

214907-30-9Relevant academic research and scientific papers

Coupling of Trifluoroacetaldehyde N-Triftosylhydrazone with Organoboronic Acids for the Synthesis of gem-Difluoroalkenes

Ma, Yu,Reddy, Bhoomireddy Rajendra Prasad,Bi, Xihe

, p. 9860 - 9863 (2019/12/24)

The synthesis of alkyl gem-difluoroalkenes remains a difficult task in organic synthesis. Here, we report a general and efficient approach for tackling this problem by gem-difluoroolefination of trifluoroacetaldehyde N-triftosylhydrazone with organoboronic acids. This protocol is operationally simple, free of transition metals, and suitable for a broad range of organoboronic acids. Moreover, the utility of the products was demonstrated by further conversion of the gem-difluorovinyl group.

Synthesis of α-Borylated Ketones by Regioselective Wacker Oxidation of Alkenylboronates

Corless, Victoria B.,Holownia, Aleksandra,Foy, Hayden,Mendoza-Sanchez, Rodrigo,Adachi, Shinya,Dudding, Travis,Yudin, Andrei K.

supporting information, p. 5300 - 5303 (2018/09/12)

As part of a program aimed at metal-catalyzed oxidative transformations of molecules with carbon-metalloid bonds, the synthesis of α-borylated ketones is reported via regioselective TBHP-mediated Wacker-type oxidation of N-methyliminodiacetic acid (MIDA)-protected alkenylboronates. The observed regioselectivity correlates with the hemilabile nature of the B-N dative bond in the MIDA boronate functional group, which allows boron to guide selectivity through a neighboring group effect.

Rhodium-catalyzed asymmetric conjugate addition of arylboroxines to borylalkenes: Asymmetric synthesis of β-arylalkylboranes

Sasaki, Keigo,Hayashi, Tamio

supporting information; experimental part, p. 8145 - 8147 (2011/02/22)

Asymmetric conjugate addition of arylboroxines to borylalkenes proceed in the presence of a chiral bisphosphine/rhodium complex as a catalyst to give chiral β-arylalkylboranes with high enantioselectivities (see scheme). [O]=H2O2/NaOH.

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