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10160-28-8

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10160-28-8 Usage

General Description

8-Nonyn-1-ol is a chemical compound with the molecular formula C9H18O. It is a linear, unsaturated alcohol with a nonyl (C9H19) chain and a hydroxyl group (-OH) attached to the first carbon atom. 8-Nonyn-1-ol is a colorless liquid with a faint odor and is insoluble in water but soluble in organic solvents. 8-Nonyn-1-ol is commonly used as a surfactant and emulsifier in industrial and household products, as well as a precursor in the synthesis of fragrances and flavorings. It is also utilized in the production of lubricants, plasticizers, and other chemical intermediates. 8-Nonyn-1-ol is flammable and should be handled with caution.

Check Digit Verification of cas no

The CAS Registry Mumber 10160-28-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,6 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10160-28:
(7*1)+(6*0)+(5*1)+(4*6)+(3*0)+(2*2)+(1*8)=48
48 % 10 = 8
So 10160-28-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O/c1-2-3-4-5-6-7-8-9-10/h1,10H,3-9H2

10160-28-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name non-8-yn-1-ol

1.2 Other means of identification

Product number -
Other names 1-Hydroxynon-8-yne

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:10160-28-8 SDS

10160-28-8Relevant articles and documents

Streamlined One-Pot Synthesis of Nitro Fatty Acids

El Rady, Eman A.,Hassan, Mohamed,Krieg, Sara-Cathrin,Maier, Thorsten J.,Manolikakes, Georg,Ndefo Nde, Cedric,Raslan, Mohamed A.,Roos, Jessica,Sadek, Kamal U.

, p. 2239 - 2252 (2021/07/22)

A novel method for the synthesis of nitro fatty acids (NFAs), an intriguing class of endogenously occurring lipid mediators, is reported. This one-pot procedure enables the controlled and stereoselective construction of nitro fatty acids from a simple set of common building blocks in a highly facile manner. Thereby, this methodology offers a streamlined, highly modular access to naturally occurring nitro fatty acids as well as non-natural NFA derivatives.

Enantioselective Rhodium-Catalyzed Dimerization of ω-Allenyl Carboxylic Acids: Straightforward Synthesis of C2-Symmetric Macrodiolides

Steib, Philip,Breit, Bernhard

, p. 6572 - 6576 (2018/05/08)

Herein, we report on the first enantioselective and atom-efficient catalytic one-step dimerization method to selectively transform ω-allenyl carboxylic acids into C2-symmetric 14- to 28-membered bismacrolactones (macrodiolides). This convenient asymmetric access serves as an attractive route towards multiple naturally occuring homodimeric macrocyclic scaffolds and demonstrates excellent efficiency to construct the complex, symmetric core structures. By utilizing a rhodium catalyst with a modified chiral cyclopentylidene-diop ligand, the desired diolides were obtained in good to high yields, high diastereoselectivity, and excellent enantioselectivity.

20-HETE RECEPTOR (GPR75) ANTAGONISTS AND METHODS OF USE

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Paragraph 00129, (2017/09/27)

The present invention concerns compounds and their use to treat cardiovascular disease, renal disease, thrombic disease, stroke, metabolic syndrome, cell proliferation, and ischemic cardiovascular disorders. Compounds of the present invention display sign

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