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101273-46-5

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101273-46-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101273-46-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,2,7 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 101273-46:
(8*1)+(7*0)+(6*1)+(5*2)+(4*7)+(3*3)+(2*4)+(1*6)=75
75 % 10 = 5
So 101273-46-5 is a valid CAS Registry Number.

101273-46-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-methylphenyl)isoquinoline

1.2 Other means of identification

Product number -
Other names 1-(p-tolyl)isoquinoline

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:101273-46-5 SDS

101273-46-5Relevant articles and documents

Orange-Red Phosphorescent Iridium(III) Complexes Bearing Bisphosphine Ligands: Synthesis, Photophysical and Electrochemical Properties, and DFT Calculations

Li, Gao-Nan,Dou, Shao-Bin,Zheng, Tao,Chen, Xiao-Qing,Yang, Xiao-Han,Wang, Shuang,Sun, Wei,Chen, Guang-Ying,Mo, Zheng-Rong,Niu, Zhi-Gang

, p. 78 - 86 (2018)

Nine new phosphorus-coordinated iridium(III) complexes of the form [Ir(C^N)2(P^P)]PF6, [Ir(F-piq)2(xantphos)]PF6 (1), [Ir(F-piq)2(binap)]PF6 (2), [Ir(F-piq)2/sub

Copper-catalyzed cross-coupling of aryl-, primary alkyl-, and secondary alkylboranes with heteroaryl bromides

Bergmann, Allison M.,Oldham, Adam M.,You, Wei,Brown, M. Kevin

, p. 5381 - 5384 (2018)

A method for the Cu-catalyzed cross-coupling of both aryl and alkylboranes with aryl bromides is described. The method employs an inexpensive Cu-catalyst and functions for a variety of heterocyclic as well as electron deficient aryl bromides. In addition, aryl iodides of varying substitution patterns and electronic properties work well.

Synthesis of a heptaarylisoquinoline: Unusual disconnection for constructing isoquinoline frameworks

Asako, Takashi,Suzuki, Shin,Itami, Kenichiro,Muto, Kei,Yamaguchi, Junichiro

, p. 968 - 970 (2018)

In a novel disconnection of isoquinoline ring synthesis at the C7C8/C4aC8a bonds, these bonds can be formed by a [4+2] cycloaddition between thiophene S,S-dioxide and alkynes. With a subsequent CH arylation of the resulting hexaarylisoquinoline at the C3 position, the synthesis of a fully substituted isoquinoline has been achieved.

Phase-selective modulation of TiO2 for visible light-driven C–H arylation: Tuning of absorption and adsorptivity

Bak, Sora,Lee, Sae Mi,Hwang, Hee Min,Lee, Hyoyoung

, p. 71 - 76 (2019/05/08)

To understand and modify TiO2 for organic photoreaction, two points are important: improving light absorption and retaining adsorption sites for organic reagents. Herein, we tuning the absorption and adsorption of TiO2 by introducing

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