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197223-39-5

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197223-39-5 Usage

General Description

3,5-Di-tert-butylphenylboronic acid is a chemical compound with the formula C14H23BO2. It is a boronic acid derivative that is commonly used in organic synthesis as a reagent for the Suzuki-Miyaura coupling reaction, which is a widely utilized method for forming carbon-carbon bonds. 3,5-DI-T-BUTYLPHENYLBORONIC ACID contains a boron atom chelated to a phenyl ring with two tert-butyl groups at the 3 and 5 positions. It is a white crystalline solid that is stable under normal conditions and is typically handled and stored in air-free environments. 3,5-Di-tert-butylphenylboronic acid is a valuable tool in organic chemistry for constructing complex molecular structures.

Check Digit Verification of cas no

The CAS Registry Mumber 197223-39-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,7,2,2 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 197223-39:
(8*1)+(7*9)+(6*7)+(5*2)+(4*2)+(3*3)+(2*3)+(1*9)=155
155 % 10 = 5
So 197223-39-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H23BO2/c1-13(2,3)10-7-11(14(4,5)6)9-12(8-10)15(16)17/h7-9,16-17H,1-6H3

197223-39-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (3,5-ditert-butylphenyl)boronic acid

1.2 Other means of identification

Product number -
Other names (3,5-Di-tert-butylphenyl)boronic acid

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:197223-39-5 SDS

197223-39-5Relevant articles and documents

Ruthenium(II)- Bipyridyl with extended π-system: Improved thermo-stable sensitizer for efficient and long-term durable dye sensitized solar cells

Chandrasekharam,Rajkumar,Rao, Ch. Srinivasa,Suresh,Reddy,Soujanya

, p. 555 - 565 (2011)

A new extended thermo-stable high molar extinction coefficient bipyridyl ruthenium(II) complex "cis-Ru(4,4'-bis(3,5-di-tert-butylphenyl)-2,2'- bipyridine)(Ln)(NCS)2 H101", where Ln = 4,4'-dicarboxylic acid-2,2'-bipyridine; was synthesized and c

Biaryl Group 4 Metal Complexes as Non-Metallocene Catalysts for Polyethylene with Long Chain Branching

Gragert, Maria M.,Tomov, Atanas K.,Bettonville, Serge,Pannier, Ga?lle,White, Andrew J. P.,Britovsek, George J. P.

, p. 4088 - 4092 (2020)

A series of biaryl Group 4 complexes with a bidentate and a tridentate pincer ligand have been synthesized and characterized. The complexes have been applied as metallocene analogues for the controlled polymerization of ethylene and the copolymerization of ethylene and 1-hexene, with a particular focus on the control of the degree of long chain branching in these polymers.

Meso-substituted boron-dipyrromethene compounds: synthesis, tunable solid-state emission, and application in blue-driven LEDs

Liu, Hao,Su, Huan,Chen, Zhiyuan,Zhu, Senqiang,Liu, Rui,Zhu, Hongjun

, p. 1697 - 1705 (2021/07/10)

In this work, we depict the synthesis and characterization of a series of meso-substituted boron-dipyrromethene (BODIPY) compounds. Their optical and electrochemical properties were investigated systematically. All these compounds exhibited intense absorption bands in the ultraviolet (UV) and visible regions, which arise from the π–π* transitions based on their BODIPY core segments. By comparing electron-withdrawing substituents and electron-donating substituents, we found that these compounds exhibited some similar photophysical properties but exhibited different fluorescence in the solid state. All compounds were highly emissive in dichloromethane at room temperature (λem = 512–523 nm, ΦPL > 0.9). When these compounds were applied in blue-driven light-emitting diodes (LEDs) as light-emitting materials, the devices showed luminescence efficiency ranging from 1.09 to 34.13 lm/W. Their luminescence and electrochemical properties could be used for understanding the structure–property relationship of BODIPY compounds and developing functional fluorescent materials.

Bimetal complex with aryloxy ether skeleton, and preparation method and application thereof

-

Paragraph 0129; 0136; 0138, (2020/11/26)

The invention provides a bimetallic complex with an aryloxy ether skeleton, and a preparation method and application of the bimetallic complex. The bimetallic complex has a structural expression as shown in the specification. A catalytic system of the bimetallic complex shows very good catalytic activity and thermal stability when being used for catalyzing olefin homopolymerization or olefin/alphaolefin copolymerization reactions, and a polymerization product generated by catalysis has relatively high molecular weight and a high alpha-olefin insertion rate and has a very good industrial application prospect.

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