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8-(3-octylthiiran-2-yl)octanoic acid is a complex organic compound with the molecular formula C16H30O3S. It is characterized by a unique structure that includes an octanoic acid chain, which is an eight-carbon fatty acid, and a 3-octylthiiran-2-yl group, which is a cyclic sulfur-containing moiety attached to the eighth carbon of the octanoic acid. 8-(3-octylthiiran-2-yl)octanoic acid is known for its potential applications in various chemical and pharmaceutical industries, particularly in the synthesis of surfactants, detergents, and other specialty chemicals. Its specific properties, such as solubility and reactivity, can be influenced by the presence of the sulfur atom and the length of the hydrocarbon chains, making it a versatile building block for the creation of new materials with tailored characteristics.

3075-89-6

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3075-89-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3075-89-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,7 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3075-89:
(6*3)+(5*0)+(4*7)+(3*5)+(2*8)+(1*9)=86
86 % 10 = 6
So 3075-89-6 is a valid CAS Registry Number.

3075-89-6SDS

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 8-(3-octylthiiran-2-yl)octanoic acid

1.2 Other means of identification

Product number -
Other names 2-Thiiraneoctanoicacid,3-octyl

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:3075-89-6 SDS

3075-89-6Relevant academic research and scientific papers

REACTIONS OF HIGHER ALIPHATIC cis- AND trans-EPITHIO ACIDS WITH HYDROGEN BROMIDE AND ANILINE

Kuranova, I. L.,Shestakova, N. N.

, p. 1268 - 1275 (2007/10/02)

The position isomers of threo- and erythro-bromomercaptooctadecanoic and anilinomercaptooctadecanoic esters were isolated by the reactions of cis- and trans-epithiooctadecanoic esters with hydrogen bromide and aniline.The PMR and mass spectra of the compo

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