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2-(4-TERT-BUTYLPHENYL)ETHYLAMINE, with the molecular formula C14H23N, is a secondary amine characterized by a nitrogen atom bonded to two carbon atoms. This colorless liquid at room temperature is known for its stability and resistance to oxidation, attributed to the presence of a tert-butyl group in its structure. It has been recognized for its potential as a building block in organic synthesis and drug development, and is utilized in research and development applications.

91552-82-8

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91552-82-8 Usage

Uses

Used in Pharmaceutical Industry:
2-(4-TERT-BUTYLPHENYL)ETHYLAMINE is used as a raw material for the production of various pharmaceuticals and organic compounds. Its unique structure and properties make it a valuable component in the synthesis of new drugs and medicinal agents.
Used in Organic Synthesis:
2-(4-TERT-BUTYLPHENYL)ETHYLAMINE is used as a building block in organic synthesis for creating a range of organic compounds. Its versatility in forming different chemical bonds and its stability contribute to its utility in this field.
Used in Research and Development:
2-(4-TERT-BUTYLPHENYL)ETHYLAMINE is utilized in research and development applications, where its properties are explored for potential new uses and to enhance existing processes in chemical and pharmaceutical research.

Check Digit Verification of cas no

The CAS Registry Mumber 91552-82-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,5,5 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 91552-82:
(7*9)+(6*1)+(5*5)+(4*5)+(3*2)+(2*8)+(1*2)=138
138 % 10 = 8
So 91552-82-8 is a valid CAS Registry Number.

91552-82-8SDS

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 2-(4-(tert-Butyl)phenyl)ethanamine

1.2 Other means of identification

Product number -
Other names 2-(4-tert-butylphenyl)ethanamine

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:91552-82-8 SDS

91552-82-8Relevant academic research and scientific papers

Direct Access to Primary Amines from Alkenes by Selective Metal-Free Hydroamination

Du, Yi-Dan,Chen, Bi-Hong,Shu, Wei

supporting information, p. 9875 - 9880 (2021/03/29)

Direct and selective synthesis of primary amines from easily available precursors is attractive yet challenging. Herein, we report the rapid synthesis of primary amines from alkenes via metal-free regioselective hydroamination at room temperature. Ammonium carbonate was used as ammonia surrogate for the first time, allowing for efficient conversion of terminal and internal alkenes into linear, α-branched, and α-tertiary primary amines under mild conditions. This method provides a straightforward and powerful approach to a wide spectrum of advanced, highly functionalized primary amines which are of particular interest in pharmaceutical chemistry and other areas.

PROCESS FOR PRODUCING DIHYDROISOQUINOLINE ZWITTERIONS

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Page/Page column 16, (2008/06/13)

This invention relates to a preparation of zwitterionic sulfates of substituted or unsubstituted 3, 4-dihydroisoquinoline.

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