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Cyclohexanol, 1-(3-hydroxy-1-butynyl)-, also known as 1-(3-hydroxy-1-butynyl)cyclohexanol, is an organic compound with the molecular formula C10H16O2. It is a derivative of cyclohexanol, featuring a 3-hydroxy-1-butynyl group attached to the cyclohexane ring. Cyclohexanol,1-(3-hydroxy-1-butynyl)- is characterized by its unique structure, which includes a cyclohexane ring, a hydroxyl group, and a butynyl group. It is used in various chemical reactions and synthesis processes, particularly in the production of pharmaceuticals and other specialty chemicals. The compound's properties, such as its reactivity and solubility, make it a valuable intermediate in organic synthesis.

5111-47-7

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5111-47-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5111-47-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,1 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5111-47:
(6*5)+(5*1)+(4*1)+(3*1)+(2*4)+(1*7)=57
57 % 10 = 7
So 5111-47-7 is a valid CAS Registry Number.

5111-47-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3'-hydroxy-1-butynyl)cyclohexanol

1.2 Other means of identification

Product number -
Other names 1-(3-Hydroxy-1-butynyl)cyclohexan-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:5111-47-7 SDS

5111-47-7Relevant academic research and scientific papers

CeCl3-mediated addition of acetylenic bis-lithium salts to aldehydes and ketones: An efficient route to bis-substituted alkyne diols

Princival, Jefferson Luiz,Ferreira, Jeiely Gomes

supporting information, p. 3525 - 3528 (2017/10/06)

An efficient, chemoselective protocol to access propargylic diols via a CeCl3-mediated addition reaction is reported. Propargylic alcohols were transformed into the corresponding acetylenic bis-lithium salt intermediates, which react with aldehydes and ketones in the presence of dry CeCl3 to furnish the corresponding bis-substituted alkyne diols. This protocol does not involve protection-deprotection or transmetallation steps, and allows the use of poorly reactive or highly enolizable substrates.

Synthesis and in vitro evaluation of (R), (S) and (R/S)-2-hexyne-1,4-diol, a natural product produced by fungus Clitocybe catinus, and related analogs as potential anticancer agents

Princival, Iza Mirela R.G.,Ferreira, Jeiely G.,Silva, Teresinha G.,Aguiar, Jaciana S.,Princival, Jefferson L.

supporting information, p. 2839 - 2842 (2016/06/09)

The search for natural products and related analogs as potential anticancer agents has seen a significant growth worldwide. Since small sized propargylic diols can be found in nature and chemically synthesized, their evaluation against cancer cells has been of great interest, being a topic of relevance to be investigated. For this purpose, a scalable approach aiming at the synthesis of several propargylic diols and their bioactivity against seven tumor cell lines were evaluated. Interestingly, when the compound 1a, a natural product produced by fungus Clitocybe catinus, was tested in its racemic mixture a more effective activity was observed if compared when enantiopure R-1a or S-1a were tested separately.

Regiocontrolled Formation of 4,5-Dihydro-3(2H)-furanones from 2-Butyne-1,4-diol Derivatives. Synthesis of Bullatenone and Geiparvarin

Saimoto, Hiroyuki,Hiyama, Tamejiro,Nozaki, Hitosi

, p. 3078 - 3087 (2007/10/02)

Two new methods for selective hydration of 1,1,4-trisubstituted 2-butyne-1,4-diols (1) to give 4,5-dihydro-3(2H)-furanone derivatives are reported.The first involves selective monoacetylation of the less hindered hydroxyl group of 1 followed by Ag(I)-cata

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