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103273-01-4

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103273-01-4 Usage

General Description

2-Bromo-4-tert-butylaniline is a chemical compound commonly used in the field of organic synthesis. This chemical, also known as 4-tert-Butyl-2-bromoaniline, is characterized by its highly specific structure, which includes a bromine atom and a tert-butyl group attached to an aniline base. It is known for its high reactivity, making it valuable in various chemical reactions, such as coupling reactions. The compound is slightly hazardous in case of skin contact, eye contact, ingestion, or inhalation and is to be handled with proper safety precautions.

Check Digit Verification of cas no

The CAS Registry Mumber 103273-01-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,2,7 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 103273-01:
(8*1)+(7*0)+(6*3)+(5*2)+(4*7)+(3*3)+(2*0)+(1*1)=74
74 % 10 = 4
So 103273-01-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H14BrN/c1-10(2,3)7-4-5-9(12)8(11)6-7/h4-6H,12H2,1-3H3

103273-01-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-BROMO-4-TERT-BUTYLANILINE

1.2 Other means of identification

Product number -
Other names 1-Amino-2-brom-4-tert-butylbenzol

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:103273-01-4 SDS

103273-01-4Relevant articles and documents

Highly efficient dye-sensitized solar cells based on panchromatic ruthenium sensitizers with quinolinylbipyridine anchors

Chou, Chun-Cheng,Hu, Fa-Chun,Yeh, Hsiu-Hsuan,Wu, Hsin-Pei,Chi, Yun,Clifford, John N.,Palomares, Emilio,Liu, Shih-Hung,Chou, Pi-Tai,Lee, Gene-Hsiang

, p. 178 - 183 (2014)

Panchromatic RuII sensitizers TF-30-TF-33 bearing a new class of 6-quinolin-8-yl-2,2′-bipyridine anchor were synthesized and tested under AM1.5 G simulated solar irradiation. Their increased π conjugation relative to that of the traditional 2,2

Benzazole derivatives and organic electroluminescent device including the same

-

Paragraph 0262-0265, (2021/05/25)

Provided is a benzazole derivative which effectively absorbs a high-energy external light source in the UV region and thus minimizes damage to organic materials in an organic electroluminescent device, thereby contributing to a substantial improvement in the service life of the organic electroluminescent device. An organic electroluminescent device according to the present invention comprises: a first electrode; a second electrode; at least one organic layer disposed between the first electrode and the second electrode; and a capping layer, wherein the organic layer or the capping layer comprises a benzazole derivative represented by chemical formula 1 according to the present invention.

Selective Thiocyanation and Aromatic Amination to Achieve Organized Annulation of Enaminone with Thiocyanate

Feng, Xukai,Leng, Xin,Li, Jianli,Li, Yao,Liu, Hua,Liu, Lang,Liu, Ping,She, Mengyao,Zhang, Jun,Zhang, Shengyong,Zheng, Tingting

supporting information, p. 8396 - 8401 (2021/11/17)

A tandem insertion of thiocyanate to enamine was performed for the regioselective synthesis of multisubstituted benzoimidazo[2,1-b]thiazoles. This method was shown to be effective in addressing the issue of isomerization encountered in common strategies. With a change made to the leading group on the aniline fragment of enamine, the reaction achieved different transformations, thus enabling multisubstituted benzo[4,5]imidazo[2,1-b]thiazoles and thiazoles in satisfactory yields.

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