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1H-Indole, 2-(1H-indol-3-ylmethyl)-3-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70423-69-7

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70423-69-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70423-69-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,4,2 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 70423-69:
(7*7)+(6*0)+(5*4)+(4*2)+(3*3)+(2*6)+(1*9)=107
107 % 10 = 7
So 70423-69-7 is a valid CAS Registry Number.

70423-69-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(1H-indol-3-yl)methyl]-3-methyl-1H-indole

1.2 Other means of identification

Product number -
Other names 2-(indol-3-ylmethyl)-3-methylindole

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:70423-69-7 SDS

70423-69-7Downstream Products

70423-69-7Relevant academic research and scientific papers

Photocatalytic Redox-Neutral Approach to Diarylmethanes

Guo, Guozhe,Yuan, Yong,Bao, Xiazhen,Cao, Xuehui,Sang, Tongzhi,Wang, Jiayuan,Huo, Congde

supporting information, p. 6936 - 6940 (2021/09/14)

We report a visible-light induced redox-neutral decarboxylative cross coupling reaction of indole-3-acetic acid NHPI esters with indoles using a Ru photosensitizer to deliver a wide range of symmetrical and unsymmetrical 3,3′-bisindolylmethane derivatives. Furthermore, the reaction is readily adapted to the preparation of a wide variety of diarylmethane derivatives.

Novel method for synthesis of unsymmetrical bis(indolyl)alkanes catalyzed by ceric ammonium nitrate (CAN) under ultrasonic irradiation

Zeng, Xiao-Fei,Ji, Shun-Jun,Wang, Shun-Yi

, p. 10235 - 10241 (2007/10/03)

The reaction of indole with (1H-indol-3-yl)(alkyl) methanol was catalyzed efficiently by ceric ammonium nitrate under ultrasonic irradiation to afford the unsymmetrical bis(indolyl)alkane in good to excellent yields.

Reductive Deoxygenation of Aryl Aldehydes and Ketones and Benzylic, Allylic, and Tertiary Alcohols by ZnI2-NaCNBH3

Lau, C. K.,Dufresne, Claude,Belanger, Patrice C.,Pietre, Sylvie,Scheigetz, John

, p. 3038 - 3043 (2007/10/02)

Sodium cyanoborohydride in the presence of zinc iodide is found to exhibit unique and selective reducing properties.The reagents reduce aryl aldehydes and ketones as well as benzylic, allylic, and tertiary alcohols to the corresponding hydrocarbons.

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