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14597-26-3

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14597-26-3 Usage

General Description

4-(DIMETHYLAMINO)BUT-2-YN-1-OL is a chemical compound with the molecular formula C6H11NO. It is an aliphatic amine with a hydroxyl functional group and a triple bond between the second and third carbon atoms. 4-(DIMETHYLAMINO)BUT-2-YN-1-OL is used in organic synthesis as a reagent for the introduction of the dimethylamino group and the alkyne functional group into organic molecules. It has also been studied for its potential use as a catalyst in various chemical reactions. Additionally, 4-(DIMETHYLAMINO)BUT-2-YN-1-OL may have applications in medicinal chemistry and pharmaceutical research due to its unique structure and potential biological activity.

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.

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

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