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2-Methyl-N-(thiophen-2-ylmethyl)propan-2-amine is a chemical compound characterized by the molecular formula C10H15NS. It is a tertiary amine with a methyl substitution on the alpha carbon and a thiophen-2-ylmethyl substitution on the nitrogen atom. 2-Methyl-N-(thiophen-2-ylMethyl)propan-2-aMine is known for its unique structural features, which make it a valuable intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its potential applications in medicinal chemistry and drug discovery are also noteworthy, although it requires careful handling and adherence to safety precautions due to its potential hazards.

344257-87-0

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344257-87-0 Usage

Uses

Used in Organic Synthesis:
2-Methyl-N-(thiophen-2-ylmethyl)propan-2-amine is used as a key intermediate in organic synthesis for the production of a variety of chemical compounds. Its unique structural features allow for versatile reactions and transformations, making it a valuable building block in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Methyl-N-(thiophen-2-ylmethyl)propan-2-amine is used as an intermediate in the synthesis of various drugs. Its unique structural features enable the development of new pharmaceuticals with novel mechanisms of action and improved therapeutic properties.
Used in Agrochemical Industry:
2-Methyl-N-(thiophen-2-ylmethyl)propan-2-amine is also used in the agrochemical industry as an intermediate in the production of various agrochemicals, such as pesticides and herbicides. Its unique structural features contribute to the development of more effective and environmentally friendly agrochemicals.
Used in Medicinal Chemistry and Drug Discovery:
Due to its unique structural features, 2-Methyl-N-(thiophen-2-ylmethyl)propan-2-amine has potential applications in medicinal chemistry and drug discovery. It can be used as a starting material or a building block for the design and synthesis of new drug candidates with improved pharmacological properties and therapeutic potential.
Safety Precautions:
It is important to handle 2-Methyl-N-(thiophen-2-ylmethyl)propan-2-amine with care and follow proper safety precautions due to its potential hazards. This includes wearing appropriate personal protective equipment, working in a well-ventilated area, and following established safety guidelines to minimize the risk of exposure and adverse effects.

Check Digit Verification of cas no

The CAS Registry Mumber 344257-87-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,4,2,5 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 344257-87:
(8*3)+(7*4)+(6*4)+(5*2)+(4*5)+(3*7)+(2*8)+(1*7)=150
150 % 10 = 0
So 344257-87-0 is a valid CAS Registry Number.

344257-87-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-N-(thiophen-2-ylmethyl)propan-2-amine

1.2 Other means of identification

Product number -
Other names N-t-butyl-N-thenylamine

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:344257-87-0 SDS

344257-87-0Downstream Products

344257-87-0Relevant articles and documents

Elimination reactions of N-alkyl-N-chlorothenylamines promoted by MeONa-MeOH and Et2NH-MeCN. Effect of the β-aryl group on the imine-forming transition state

Pyun, Sang Yong,Lee, Dong Choon,Seung, Yoon Je,Cho, Bong Rae

, p. 5327 - 5330 (2007/10/03)

Elimination reactions of N-alkyl-N-chlorothenylamines 1-4 with MeONa-MeOH and Et2NH-MeCN have been studied kinetically. The elimination reactions are regiospecific, producing only the conjugated imines. The reactions are second order and exhibit substantial values of Hammett ρ and k H/kD, and an E2 mechanism is evident. The relative rates of elimination for Me/Et/i-Pr/i-Bu substituents are 1/0.5/0.2/0.02 with MeONa-MeOH and 1/0.4/0.2/0.06 with Et2NH-MeCN. The transition state structure changes toward more product-like as the base is changed from MeONa-MeOH to Et2NH-MeCN. Comparison with existing data reveals that the structure of the transition state is relatively insensitive to the β-aryl group variation.

SYNTHESIS AND STUDY OF THE LIGHT-STABILIZING ACTIVITY OF SOME DITHIOCARBAMATES THAT INCLUDE A HETEROAROMATIC RING

Gol'dfarb, Ya. L.,Ostapenko, E'. G.,Ivanov, V.B.,Efremkin, A. F.,Litvinov, V. P.

, p. 1148 - 1153 (2007/10/02)

A number of new dithiocarbamates of transition metals that contain thiophene, furan, benzothiophene, and benzoselenophene rings were synthesized.The compounds obtained were investigated as light stabilizers for polymers.It is shown that the effectiv

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