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22DIETHYL11BIPHENYL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13049-35-9

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13049-35-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13049-35-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,4 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13049-35:
(7*1)+(6*3)+(5*0)+(4*4)+(3*9)+(2*3)+(1*5)=79
79 % 10 = 9
So 13049-35-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H18/c1-3-13-9-5-7-11-15(13)16-12-8-6-10-14(16)4-2/h5-12H,3-4H2,1-2H3

13049-35-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethyl-2-(2-ethylphenyl)benzene

1.2 Other means of identification

Product number -
Other names diethylbiphenyl

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:13049-35-9 SDS

13049-35-9Downstream Products

13049-35-9Relevant academic research and scientific papers

An active, general, and long-lived palladium catalyst for cross-couplings of deactivated (hetero)aryl chlorides and bromides with arylboronic acids

Hoshi, Takashi,Honma, Tomonobu,Mori, Ayako,Konishi, Maki,Sato, Tsutomu,Hagiwara, Hisahiro,Suzuki, Toshio

, p. 11513 - 11524 (2013/12/04)

An active, general, and long-lived palladium catalyst for Suzuki-Miyaura reactions of aryl and heteroaryl chlorides deactivated by steric hindrance, electron richness, and coordinating functional groups is reported. In reactions of arylbromide bearing two o-tert-butyl substituents, C(sp3)-H arylation of the tert-butyl group, rather than the Suzuki-Miyaura reaction, proceeded in excellent yield. The key to the success of the reactions was the development of biphenylene-substituted dicyclohexylruthenocenylphosphine (CyR-Phos) as a supporting ligand.

PALLADIUM(II)-CATALYZED OXIDATIVE COUPLING OF ARENES BY THALLIUM(III)

Yatsimirsky, Anatoly K.,Deiko, Sergei A.,Ryabov, Alexander D.

, p. 2381 - 2392 (2007/10/02)

Oxidation of benzenes with electron-donating and moderate electron-withdrawing substituents by thallium(III) trifluoroacetate in the presence of catalytic amounts of palladium(II) acetate affords biaryls in good yields.The GLC study of the isomer distribution has shown that 4,4'-biaryls are the major products.Thus, the 4,4'-biaryls can be easily isolated either by recrystallization or column chromatography.The competitive experiments and kinetic study using arenes and arylthallium derivatives as starting materials as well as quenching experiments have demonstrated the first step of the reaction to be fast thallation of arene to form arylthallium intermediate ArTl(OOCCF3)2.The latter undergoes the rate-determining transmetallation step reacting with monomeric complex Pd(OAc)2, which is formed upon depolymerization of trimer Pd3(OAc)6.Subsequent fast decomposition of arylpalladium species gives the final reaction products.The thallation of arene and substitution of TlIII for PdII in ArTl(OOCCF3)2 are characterized by the slopes of Hammet plots of -5.6 (?+) and -3.0 (?), respectively.

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