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Benzene, 1-azido-2-(2-phenylethenyl)-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89100-39-0

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89100-39-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89100-39-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,1,0 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 89100-39:
(7*8)+(6*9)+(5*1)+(4*0)+(3*0)+(2*3)+(1*9)=130
130 % 10 = 0
So 89100-39-0 is a valid CAS Registry Number.

89100-39-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-azido-2-((Z)-styryl)benzene

1.2 Other means of identification

Product number -
Other names cis-o-azidostilbene

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:89100-39-0 SDS

89100-39-0Upstream product

89100-39-0Downstream Products

89100-39-0Relevant academic research and scientific papers

Iron-Catalyzed Intramolecular Aminations of C(sp3)?H Bonds in Alkylaryl Azides

Alt, Isabel T.,Guttroff, Claudia,Plietker, Bernd

supporting information, p. 10582 - 10586 (2017/08/22)

The nucleophilic iron complex Bu4N[Fe(CO)3(NO)] (TBA[Fe]) catalyzes the direct intramolecular amination of unactivated C(sp3)?H bonds in alkylaryl azides, which results in the formation of substituted indoline and tetrahydroquinoline derivatives.

Iron-Catalyzed Intramolecular C(sp2)-H Amination

Alt, Isabel T.,Plietker, Bernd

supporting information, p. 1519 - 1522 (2016/02/14)

The nucleophilic iron complex Bu4N[Fe(CO)3(NO)] (TBA[Fe]) catalyzes the direct intramolecular C-H amination of α-azidobiaryls and (azidoaryl)alkenes into the corresponding carbazoles and indoles, respectively, under mild conditions and with low catalyst loadings. These features and the broad functional-group tolerance render this method a particularly attractive alternative to established noble-metal-based procedures.

Synthesis of 2-Substituted Indoles through Visible Light-Induced Photocatalytic Cyclizations of Styryl Azides

Xia, Xu-Dong,Xuan, Jun,Wang, Qiang,Lu, Liang-Qiu,Chen, Jia-Rong,Xiao, Wen-Jing

supporting information, p. 2807 - 2812 (2016/02/18)

A visible light-induced photocatalytic intramolecular cyclization of styryl azides has been developed in the presence of the ruthenium complex Ru(bpy)3Cl2 (0.5 mol%) as photocatalyst at room temperature. The present photocatalytic strategy features operational simplicity as well as high functional group tolerance, and provides a facile access to various 2-substituted N-free indoles in good to excellent yields. Importantly, the present process can employ sunlight as the light source to afford the corresponding products without loss of reaction efficiency.

Dirhodium(II)-catalyzed intramolecular C-H amination of aryl azides

Shen, Meihua,Leslie, Brooke E.,Driver, Tom G.

supporting information; experimental part, p. 5056 - 5059 (2009/03/11)

(Chemical Equation Presented) Azides to indoles: Dirhodium(II)-catalyzed decomposition of aryl azides was developed as a mild, functional group tolerant method for the synthesis of indoles (see scheme).

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