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3-Cyclohexene-1-methanol, α-ethynyl-, also known as 3-(1-ethynylcyclohex-3-en-1-yl)-1-methanol or 3-(1-ethynyl-3-cyclohexen-1-yl)methanol, is an organic compound with the molecular formula C9H12O. It features a cyclohexene ring with a double bond between carbons 1 and 2, a hydroxyl group (-OH) attached to carbon 3, and an ethynyl group (-C≡CH) connected to the α-carbon (carbon 1) of the cyclohexene ring. This molecule is a versatile building block in organic synthesis, used in the preparation of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure, combining a cyclohexene ring with a reactive ethynyl group, allows for a wide range of chemical transformations and functional group modifications, making it a valuable intermediate in the synthesis of complex organic molecules.

7560-92-1

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7560-92-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7560-92-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,6 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7560-92:
(6*7)+(5*5)+(4*6)+(3*0)+(2*9)+(1*2)=111
111 % 10 = 1
So 7560-92-1 is a valid CAS Registry Number.

7560-92-1SDS

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 1-cyclohex-3-enyl-prop-2-yn-1-ol

1.2 Other means of identification

Product number -
Other names 1-Cyclohex-3-enyl-prop-2-in-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:7560-92-1 SDS

7560-92-1Relevant academic research and scientific papers

Syntheses and synthetic applications of stannylated allylic alcohols

Kazmaier, Uli,Lucas, Simon,Klein, Manuela

, p. 2429 - 2433 (2007/10/03)

Allenyl carbinols undergo regioselective hydrostannation in the presence of MoBl3, a catalyst originally developed for the hydrostannation of alkynes, giving rise to allyl stannanes. These allyl stannanes can easily be converted into useful synthetic building blocks such as allyl iodides or vinyl epoxides.

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