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2-Methylbut-3-en-2-amine, also known as 3-amino-2-methyl-2-butene, is an organic compound with the molecular formula C5H9N. It is a colorless liquid with an amine functional group and a unique alkenyl side chain. 2-methylbut-3-en-2-amine is known for its reactivity and is commonly used as a building block in the synthesis of various pharmaceuticals and chemical products.

2978-60-1

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2978-60-1 Usage

Uses

Used in Pharmaceutical Industry:
2-Methylbut-3-en-2-amine is used as a key intermediate in the synthesis of naphthyridine derivatives, which are known for their cholesterol acyltransferase inhibitory properties. These derivatives are valuable in the development of drugs targeting high cholesterol levels and related cardiovascular diseases.
Used in Chemical Synthesis:
In the chemical industry, 2-methylbut-3-en-2-amine serves as a versatile building block for the creation of various compounds with diverse applications. Its unique structure allows for further functionalization and modification, making it a valuable component in the synthesis of specialty chemicals, agrochemicals, and other industrial products.

Check Digit Verification of cas no

The CAS Registry Mumber 2978-60-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,7 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2978-60:
(6*2)+(5*9)+(4*7)+(3*8)+(2*6)+(1*0)=121
121 % 10 = 1
So 2978-60-1 is a valid CAS Registry Number.

2978-60-1SDS

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 2-methylbut-3-en-2-amine

1.2 Other means of identification

Product number -
Other names 2-methyl-3-buten-2-amine

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:2978-60-1 SDS

2978-60-1Relevant academic research and scientific papers

Palladium-catalysed N-annulation routes to indoles: The synthesis of indoles with sterically demanding N-substituents, including demethylasterriquinone A1

Fletcher, Anthony J.,Bax, Matthew N.,Willis, Michael C.

, p. 4764 - 4766 (2008/09/17)

Tandem palladium-catalysed aryl and alkenyl C-N bond formation allows the synthesis of a variety of indoles bearing sterically demanding N-substituents, including the natural product demethylasterriquinone A1. The Royal Society of Chemistry.

Primary tert- and sec-allylamines via palladium-catalyzed hydroamination and allylic substitution with hydrazine and hydroxylamine derivatives

Johns, Adam M.,Liu, Zhijian,Hartwig, John F.

, p. 7259 - 7261 (2008/09/17)

(Chemical Equation Presented) Amines of control: Palladium-catalyzed reactions of hydrazine and hydroxylamine derivatives with dienes and allylic esters form products from C-N bond formation at the more substituted position of the allyl intermediate with

Methods and compositions for treating amyloid-related diseases

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Page/Page column 165, (2010/11/24)

Methods, compounds, pharmaceutical compositions and kits are described for treating or preventing amyloid-related disease.

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