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4,5-Dimethyl-2-phenyl-1,3,2-dioxaborolane is an organic compound with the chemical formula C11H13BO2. It is a colorless liquid that is soluble in organic solvents. 4,5-Dimethyl-2-phenyl-1,3,2-dioxaborolane is a member of the 1,3,2-dioxaborolane family, which are known for their use as reagents in organic synthesis. Specifically, 4,5-Dimethyl-2-phenyl-1,3,2-dioxaborolane is used as a boron-based reagent in Suzuki-Miyaura cross-coupling reactions, a type of reaction that forms carbon-carbon bonds. It is particularly useful for the synthesis of biaryl compounds, which are important in the production of pharmaceuticals and other organic materials. The compound is also valued for its stability and ease of handling compared to other boron reagents.

6638-68-2

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6638-68-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6638-68-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6638-68:
(6*6)+(5*6)+(4*3)+(3*8)+(2*6)+(1*8)=122
122 % 10 = 2
So 6638-68-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H13BO2/c1-8-9(2)13-11(12-8)10-6-4-3-5-7-10/h3-9H,1-2H3

6638-68-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-dimethyl-2-phenyl-1,3,2-dioxaborolane

1.2 Other means of identification

Product number -
Other names 1,3,2-Dioxaborolane,4,5-dimethyl-2-phenyl

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

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

More Details:6638-68-2 SDS

6638-68-2Relevant academic research and scientific papers

Insight into Copper Catalysis: In Situ Formed Nano Cu2O in Suzuki-Miyaura Cross-Coupling of Aryl/Indolyl Boronates

Ranjani, Ganapathy,Nagarajan, Rajagopal

supporting information, p. 3974 - 3977 (2017/08/14)

A ligand-free copper catalyzed Suzuki-Miyaura coupling of 3,5-diiodopyridine with aryl and indole boronates has been explored in good to excellent yields. In situ generation of nano-Cu2O from CuCl2 under the reaction conditions has been discovered for the first time. The generality of the reaction was further demonstrated by the arylation of 5-iodopyrimidine, iodopyridines, iodobenzenes, and diiodobenzenes and resulted in good to moderate yields. Moreover, bisindole alkaloid Scalaridine A has been successfully synthesized in 60% overall yield.

Diol lipids - Communication 27. Identification of C2-C4-diols in the form of cyclic esters of phenylboric acid by the method of combined gas chromatography and mass spectrometry

Batrakov,Panosyan,Ushakov,Rozynov,Bergel'son

, p. 1662 - 1668 (2007/10/10)

1. A new method was proposed for the analysis of small quantities of C2-C4-diols, formed in the cleavage of lipids, based on combined gas-chromatography and mass spectrography of their phenylborate esters. 2. Phenylborate esters of d

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