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17171-17-4

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17171-17-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17171-17-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,7 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17171-17:
(7*1)+(6*7)+(5*1)+(4*7)+(3*1)+(2*1)+(1*7)=94
94 % 10 = 4
So 17171-17-4 is a valid CAS Registry Number.

17171-17-4SDS

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 1-methoxy-4-(3-methylphenyl)benzene

1.2 Other means of identification

Product number -
Other names 3-methyl-4'-methoxylbiphenyl

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:17171-17-4 SDS

17171-17-4Relevant articles and documents

Iridium-catalyzed ortho-arylation of benzoic acids with arenediazonium salts

Huang, Liangbin,Hackenberger, Dagmar,Goossen, Lukas J.

, p. 12607 - 12611 (2015)

In the presence of catalytic [{IrCpCl2}2] and Ag2CO3, Li2CO3 as the base, and acetone as the solvent, benzoic acids react with arenediazonium salts to give the corresponding diaryl-2-carboxylates under mild conditions. This C-H arylation process is generally applicable to diversely substituted substrates, ranging from extremely electron-rich to electron-poor derivatives. The carboxylate directing group is widely available and can be removed tracelessly or employed for further derivatization. Orthogonality to halide-based cross-couplings is achieved by the use of diazonium salts, which can be coupled even in the presence of iodo substituents. Directing rather than removed: In the presence of catalytic [{IrCpCl2}2], benzoic acids react with arenediazonium salts to give the corresponding diaryl-2-carboxylates. If desired, the carboxylate directing group can be removed by in situ protodecarboxylation.

Efficient Suzuki reaction catalyzed by recyclable clay carbapalladacycle nanocomposite in ionic liquid media

Kaur, Amanpreet,Singh, Vasundhara

, p. 1128 - 1131 (2015)

In this Letter, we report the efficient recyclability and recoverability of ionic tagged carbapalladacycle and its hybrid MMT clay-nanocomposite catalyst in ionic liquid media [TMBA]NTf2 for the Suzuki reaction. It has several distinct advantages which include the use of low levels of catalyst concentration, formation of desired products in high yields and good selectivity using chloro, bromo and iodo substituted aryl halides, and negligible formation of homo coupling products.

An efficient protocol for a Pd(OAc)2-catalyzed ligand-free Suzuki reaction in toluene

Liu, Ning,Liu, Chun,Jin, Zilin

, p. 1316 - 1320 (2010)

An efficient protocol for a Pd(OAc)2-catalyzed ligand-free Suzuki reaction of aryl bromides with arylboronic acids in the presence of K3PO4·7H2O in toluene under mild and aerobic conditions afforded cross-coupling products in good to excellent yields. Under the optimized reaction conditions (i.e., 0.5 mmol ArBr, 0.75 mmol ArB(OH)2, 1 mol Pd(OAc)2, 1.0 mmol K3PO 4·7H2O, 2 ml toluene), the Suzuki reaction between 4-nitrobromobenzene and phenylboronic acid afforded a 99 isolated yield in 5 min at 75 °C and a TOF of up to 1 188 h-1.

Porous single-crystalline palladium nanoparticles with high catalytic activities

Wang, Feng,Li, Chuanhao,Sun, Ling-Dong,Xu, Chun-Hu,Wang, Jianfang,Yu, Jimmy C.,Yan, Chun-Hua

, p. 4872 - 4876 (2012)

Palladium's pore cousin: A facile approach is described for the size-controlled preparation of porous single-crystalline Pd nanoparticles. These porous Pd nanoparticles exhibit size-independent catalytic activities for the Suzuki coupling and are more active than commercial Pd/C catalysts. Copyright

Simple alcohols promoted direct C-H arylation of unactivated arenes with aryl halides

Liu, Wei,Tian, Fei,Wang, Xiaolei,Yu, Hao,Bi, Yanlan

, p. 2983 - 2985 (2013)

Simple and cheap alcohols can promote the direct arylation of unactivated arenes with aryl iodides and bromides in the presence of potassium tert-butoxide. This transition-metal-free aromatic C-H transformation offers a cheap and easy practical way to synthesize biaryls under mild conditions. The Royal Society of Chemistry.

Graphene oxide-palladium modified Ag-AgBr: A visible-light-responsive photocatalyst for the Suzuki coupling reaction

Gao, Shutao,Shang, Ningzhao,Feng, Cheng,Wang, Chun,Wang, Zhi

, p. 39242 - 39247 (2014)

The efficient utilization of the abundant and economical solar energy has received tremendous attention due to increased environmental and energy concerns. In this report, a plasmonic Ag-AgBr photocatalyst functionalized with graphene oxide-Pd was successfully fabricated and used as an efficient visible-light-responsive photocatalyst for the Suzuki coupling reaction. The integration of plasmonic Ag-AgBr with Pd nanoparticles supported on graphene oxide enabled efficient visible light harvesting for the catalytic reaction on the heterojunction structure. A possible catalytic mechanism for the highly efficient photocatalyst is proposed. This work provides a convenient means for the design of efficient catalysts that are composed of a photocatalyst and a catalytically active transition metal for various organic transformations driven by visible light.

Nickel-catalyzed direct C-H arylation of unactivated arenes with aryl halides

Xie, Guanlei,Li, Tingyi,Qu, Xiaoming,Mao, Jincheng

, p. 48 - 52 (2011)

Ni(OAc)2·4H2O could catalyze direct C-H arylation of unactivated arenes with aryl halides in presence of 1,10-phenanthroline without using additives.

Sodium 2-(2-pyridin-3-ylethylamino)ethyl sulfonate: an efficient ligand and base for palladium-catalyzed Suzuki reaction in aqueous media

Pawar, Shivaji S.,Uppalla, Lavkumar S.,Shingare, Murlidhar S.,Thore, Shivaji N.

, p. 5858 - 5862 (2008)

PdCl2, N-donor ligand and base mediated Suzuki coupling reaction of aryl halides and arylboronic acid in water are described. The corresponding Suzuki products were obtained in good to excellent yields.

Palladium-catalyzed Suzuki-Miyaura reaction using aminophosphine as ligand

Cheng, Jiang,Wang, Feng,Xu, Jian-Hua,Pan, Yi,Zhang, Zhaoguo

, p. 7095 - 7098 (2003)

Suzuki-Miyaura cross-coupling reaction has been achieved under the catalysis of Pd(OAc)2 in the presence of readily accessible and easily tunable aminophosphine ligands with high efficiency under mild reaction condition.

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Dauben,Tanabe

, p. 4969,4972 (1953)

-

Visible Light Induced Aerobic Coupling of Arylboronic Acids Promoted by Hydrazone

Xia, Hongyu,Wang, Ganghu,Zhao, Dongbo,Zhu, Chunyin

supporting information, p. 922 - 929 (2022/02/10)

A visible-light-induced oxidative coupling of arylboronic acids has been developed for the synthesis of biaryls. The reaction that employs polydentate hydrazones as the bifunctional catalyst works smoothly under room temperature. It is compatible with a w

New Nickel-Based Catalytic System with Pincer Pyrrole-Functionalized N-Heterocyclic Carbene as Ligand for Suzuki-Miyaura Cross-Coupling Reactions

Guo, Zhifo,Lei, Xiangyang

supporting information, (2021/09/11)

A new catalytic system with Ni(NO3)2·6H2O as the catalyst and a pincer pyrrole-functionalized N-heterocyclic carbene as the ligand was employed in the Suzuki-Miyaura cross-coupling reactions of aryl iodides with arylboronic acids. With 5 mol% catalyst, the catalytic reactions proceeded at 160 °C, giving coupling products in isolated yields of up to 94% in short reaction times (1-4 h). The system worked efficiently with aryl iodides bearing electron-donating or electron-withdrawing groups and arylboronic acids with electron-donating groups. Steric effects were observed for both aryl iodides and arylboronic acids. It is proposed that the reactions underwent a Ni(I)/Ni(III) catalytic cycle.

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