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Benzaldehyde, 6-(1-cyclohexen-1-ylethynyl)-2,4-dihydroxy-3-methyl-, is a complex organic compound with the molecular formula C16H16O3. It is characterized by a benzaldehyde structure, which includes a benzene ring with an aldehyde group (-CHO) attached to the carbon atom at the 6th position. The molecule also features a cyclohexenyl group (a cyclohexane ring with a double bond) connected to the benzene ring through an ethynyl (triple-bonded) linker. Additionally, it has two hydroxyl (-OH) groups at the 2nd and 4th positions of the benzene ring, and a methyl (-CH3) group at the 3rd position. Benzaldehyde, 6-(1-cyclohexen-1-ylethynyl)-2,4-dihydroxy-3-methyl- is known for its potential applications in the synthesis of various pharmaceuticals and other organic compounds due to its unique structure and reactivity.

685895-60-7

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685895-60-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 685895-60-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,5,8,9 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 685895-60:
(8*6)+(7*8)+(6*5)+(5*8)+(4*9)+(3*5)+(2*6)+(1*0)=237
237 % 10 = 7
So 685895-60-7 is a valid CAS Registry Number.

685895-60-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Cyclohex-1-enylethynyl-2,4-dihydroxy-3-methyl-benzaldehyde

1.2 Other means of identification

Product number -
Other names -

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

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More Details:685895-60-7 SDS

685895-60-7Downstream Products

685895-60-7Relevant academic research and scientific papers

Synthesis of azaphilones and related molecules by employing cycloisomerization of o-alkynylbenzaldehydes

Zhu, Jianglong,Germain, Andrew R.,Porco Jr., John A.

, p. 1239 - 1243 (2004)

Right to the core: Gold(III)-catalyzed cycloisomerization of o-alkynylbenzaldehydes to 2-benzopyrylium salts and subsequent in situ oxidation have been employed to prepare the core structure of azaphilone natural products, such as the sphingosine kinase inhibitor S-15183 (see scheme, DCE = 1,2-dichloroethane, TFA = trifluoroacetic acid)), and several unnatural azaphilones.

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