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4-(DIMETHYLAMINO)BUT-2-YN-1-OL, with the molecular formula C6H11NO, is an aliphatic amine characterized by a hydroxyl functional group and a triple bond between the second and third carbon atoms. This unique structure endows it with potential applications in various fields, including organic synthesis, catalysis, and pharmaceutical research.

14597-26-3

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14597-26-3 Usage

Uses

Used in Organic Synthesis:
4-(DIMETHYLAMINO)BUT-2-YN-1-OL is used as a reagent for the introduction of the dimethylamino group and the alkyne functional group into organic molecules. Its presence in these molecules can enhance their reactivity and properties, making it a valuable component in the synthesis of various organic compounds.
Used in Catalysis:
4-(DIMETHYLAMINO)BUT-2-YN-1-OL has been studied for its potential use as a catalyst in various chemical reactions. Its unique structure allows it to facilitate and accelerate certain reactions, making it a promising candidate for use in catalysis.
Used in Medicinal Chemistry and Pharmaceutical Research:
Due to its unique structure and potential biological activity, 4-(DIMETHYLAMINO)BUT-2-YN-1-OL may have applications in medicinal chemistry and pharmaceutical research. Its properties could be harnessed to develop new drugs or improve existing ones, contributing to advancements in healthcare and medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 14597-26-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,5,9 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 14597-26:
(7*1)+(6*4)+(5*5)+(4*9)+(3*7)+(2*2)+(1*6)=123
123 % 10 = 3
So 14597-26-3 is a valid CAS Registry Number.

14597-26-3SDS

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 4-(dimethylamino)but-2-yn-1-ol

1.2 Other means of identification

Product number -
Other names 4-dimethylamino-2-butyn-1-ol

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:14597-26-3 SDS

14597-26-3Relevant articles and documents

BIS-BENZIMIDAZOLE COMPOUNDS AND METHODS OF USING SAME

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Paragraph 00787-00789, (2019/06/05)

Provided herein are compounds and methods for modulating abnormal repeat expansions of gene sequences. More particularly, provided are inhibitors of RNA and the uses of such inhibitors in regulating nucleotide repeat expansions, e.g., to treat Myotonic Dystrophy Type 1 (DM1 ), Myotonic Dystrophy Type 2 (DM2), Fuchs dystrophy, Huntington Disease, Amyotrophic Lateral Sclerosis, or Frontotemporal Dementia.

Transformations of dialkyl(4-hydroxy-2-butynyl)-(3-phenylallyl)ammonium bromides in an KOH aqueous solution or in the presence of powdered KOH

Chukhadjian,Gabrielyan,Chukhadjian,Shahkhatuni,Panosyan

experimental part, p. 418 - 424 (2012/01/13)

Under the action of a twofold excess of KOH and heating in aqueous solution, and also under the conditions of the Stevens rearrangement (with KOH powder and a small amount of methanol) dialkyl-(4-hydroxy-2-butynyl)(3- phenylallyl)ammonium bromides form dialkyl[4-(1-phenylallyl)-2,5-dihydro-2- furyl]amines. Rearrangement-cleavage reaction also occurs under the same conditions.

Aminomethylation of acetylene alcohols and their esters with gem-diamines catalyzed by complexes of d-transition and rare-earth metals

Shaibakova,Titova,Ibragimov,Dzhemilev

experimental part, p. 161 - 167 (2011/05/04)

An efficient synthetic procedure was developed for preparation of oxygen-containing propargylamines with high yields and selectivity by aminomethylation of propargyl alcohols and their esters with gem-diamines catalyzed by complexes and salts of d-transit

Convergent, short synthesis of the muscarinic superagonist iperoxo

Kloeckner, Jessica,Schmitz, Jens,Holzgrabe, Ulrike

experimental part, p. 3470 - 3472 (2010/08/20)

Up to now the availability of iperoxo, an important superagonist of the muscarinic acetylcholine receptors, was limited because the synthesis of its precursor, the iperoxo base, was characterized by low yields, laborious chromatography and low reproducibility. Here we report a robust convergent three-step synthesis by means of a Mannich reaction and nucleophilic substitution at the 3-nitro-Δ2-isoxazoline. The new route combines short reaction time, high reproducibility and an overall yield increased from 12% to 42%.

Design and synthesis of potent antileishmanial cycloalkylidene-substituted ether phospholipid derivatives

Calogeropoulou, Theodora,Angelou, Panagiotis,Detsi, Anastasia,Fragiadaki, Irene,Scoulica, Effie

, p. 897 - 908 (2008/12/20)

Two series of novel ether phospholipids (EPs) have been synthesized. The first includes cyclodecylidene-or cyclopentadecylidene-substituted EPs carrying N,N,N-trimethylammonium or N-methylpiperidino or N-methylmorpholino head groups. The second series enc

ABSOLUTE MOLECULAR WEIGHT POLYMERS AND METHODS FOR THEIR USE

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, (2008/06/13)

A process for preparing defined molecular weight polymers, particularly polyquaternary ammonium compounds, is disclosed. As the molecular weights of these compounds can be absolutely defined, rather than defined merely in terms of "number average molecular weight," these compounds are particularly useful as identification standards for other polymers which are made using conventional polymerization processes. The polyquaternary ammonium compounds described are further suitable for use as antimicrobial agents, particularly in ophthalmic compositions.

Absolute molecular weight polymers and methods for their use

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, (2008/06/13)

A process for preparing defined molecular weight polymers, particularly polyquaternary ammonium compounds, is disclosed. As the molecular weights of these compounds can be absolutely defined, rather than defined merely in terms of "number average molecular weight," these compounds are particularly useful as identification standards for other polymers which are made using conventional polymerization processes. The polyquaternary ammonium compounds described are further suitable for use as antimicrobial agents, particularly in ophthalmic compositions.

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