모든 사진(2)

문서

287822

Tri(o-tolyl)phosphine

Name: Tri(<I>o</I>-tolyl)phosphine
Brand: ALDRICH

97%

동의어(들):

P(o-tol)₃, Tris(o-tolyl)phosphine

로그인조직 및 계약 가격 보기

모든 사진(2)

About This Item

Linear Formula:

(CH₃C₆H₄)₃P

CAS Number:

6163-58-2

Molecular Weight:

304.37

Beilstein:

661212

EC Number:

228-193-9

MDL number:

MFCD00008514

UNSPSC 코드:

12352128

PubChem Substance ID:

24857295

NACRES:

NA.22

추천 제품

Slide 1 of 10

1 of 10

Sigma-Aldrich

205869

Palladium(II) acetate

Sigma-Aldrich

328774

Tris(dibenzylideneacetone)dipalladium(0)

Sigma-Aldrich

287830

Tri(p-tolyl)phosphine

Sigma-Aldrich

395102

Tris(4-methoxyphenyl)phosphine

Sigma-Aldrich

261971

Tricyclohexylphosphine

Sigma-Aldrich

578940

Tri-tert-butylphosphonium tetrafluoroborate

Sigma-Aldrich

526460

Xantphos

Sigma-Aldrich

227994

Bis(dibenzylideneacetone)palladium(0)

Sigma-Aldrich

P20009

Phenylboronic acid

Sigma-Aldrich

697230

[1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II)

Quality Level

200

분석

97%

반응 적합성

reaction type: Cross Couplings
reaction type: Silylations
reagent type: ligand
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reagent type: ligand
reaction type: Heck Reaction
reagent type: ligand
reaction type: Negishi Coupling
reagent type: ligand
reaction type: Stille Coupling
reagent type: ligand
reaction type: Suzuki-Miyaura Coupling

mp

123-125 °C (lit.)

작용기

phosphine

SMILES string

Cc1ccccc1P(c2ccccc2C)c3ccccc3C

InChI

1S/C21H21P/c1-16-10-4-7-13-19(16)22(20-14-8-5-11-17(20)2)21-15-9-6-12-18(21)3/h4-15H,1-3H3

InChI key

COIOYMYWGDAQPM-UHFFFAOYSA-N

유사한 제품을 찾으십니까? 방문 제품 비교 안내

일반 설명

Tri(o-tolyl)phosphine is a ligand used in the heck reaction and suzuki coupling of propargylic carbonates.

애플리케이션

Ligand used in a ruthenium-catalyzed direct amination of alcohols.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves

시험 성적서(COA)

제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.

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문서 라이브러리 방문

이미 열람한 고객

Slide 1 of 4

1 of 4

Sigma-Aldrich

328774

Tris(dibenzylideneacetone)dipalladium(0)

Sigma-Aldrich

383767

Tri(2-furyl)phosphine

Sigma-Aldrich

698253

Tris(3,5-dimethylphenyl)phosphine

Sigma-Aldrich

227994

Bis(dibenzylideneacetone)palladium(0)

Tuneable Emission of Polyhedral Oligomeric Silsesquioxane Based Nanostructures that Self-Assemble in the Presence of Europium(III) Ions: Reversible trans-to-cis Isomerization.

Valerio Cinà et al.

ChemPlusChem, 85(3), 391-398 (2020-03-03)

Hybrid nanostructures with switchable and reversible "blue-red-green" emission were efficiently synthesized. These nanostructures comprise polyhedral oligomeric silsesquioxanes (POSS) that behave as a nanocage that can be functionalized with terpyridine-based organic ligands, which can be easily complexed with europium (III) ions.

Bioinspired Polymer Nanocomposites Exhibit Giant Energy Density and High Efficiency at High Temperature.

Wenhan Xu et al.

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Polymer dielectrics are ubiquitous in advanced electric energy storage systems. However, the relatively low operating temperature significantly menaces their widespread application at high temperatures, such as for hybrid vehicles and aerospace power electronics. Spider silk, a natural nanocomposite comprised of

Facilely Synthesized spiro[fluorene-9,9'-phenanthren-10'-one] in Donor-Acceptor-Donor Hole-Transporting Materials for Perovskite Solar Cells.

Yih-Chun Chen et al.

ChemSusChem, 11(18), 3225-3233 (2018-07-08)

We have demonstrated two novel donor-acceptor-donor (D-A-D) hole-transport material (HTM) with spiro[fluorene-9,9'-phenanthren-10'-one] as the core structure, which can be synthesized through a low-cost process in high yield. Compared to the incorporation of the conventional HTM of commonly used 2,2',7,7'-tetrakis[N,N-di(4-methoxyphenyl)amino]-9,9'-spirobifluorene (Spiro-OMeTAD)

Tri (o-tolyl) phosphine for highly efficient Suzuki coupling of propargylic carbonates with boronic acids

Junzhe X et al.

Chemical Communications (Cambridge, England), 54, 10451-10454 (2018)

Coordination chemistry and mechanisms of metal-catalyzed CC-coupling reactions. Part 7. Heck vinylation of aryl halides with n-butyl acrylate: relevance of PC bond cleavage to catalyst deactivation

Wolfgang H A et al.

Journal of Molecular Catalysis. B, Enzymatic, 103, 133-146 (1995)

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문서

Tri(o-tolyl)phosphine

97%

About This Item

추천 제품

속성

Quality Level

분석

반응 적합성

mp

작용기

SMILES string

InChI

InChI key

설명

일반 설명

애플리케이션

안전성 정보

Storage Class Code

WGK

Flash Point (°F)

Flash Point (°C)

개인 보호 장비

문서

시험 성적서(COA)

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