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7146-27-2

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7146-27-2 Usage

Classification

Organic compound, Fatty acid derivative

Carbon backbone

11-carbon backbone

Functional groups

Thiol group at the 2-position, hydroxyethyl group at the 11-position

Applications

Synthesis of various organic compounds, potential use in pharmaceuticals and biochemistry

Additional uses

Production of surfactants and lubricants due to amphiphilic nature

Check Digit Verification of cas no

The CAS Registry Mumber 7146-27-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,4 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7146-27:
(6*7)+(5*1)+(4*4)+(3*6)+(2*2)+(1*7)=92
92 % 10 = 2
So 7146-27-2 is a valid CAS Registry Number.

7146-27-2SDS

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 11-(2-hydroxyethylsulfanyl)undecanoic acid

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7146-27-2 SDS

7146-27-2Downstream Products

7146-27-2Relevant articles and documents

Fully biobased triblock copolyesters from l-lactide and sulfur-containing castor oil derivatives: Preparation, oxidation and characterization

Beyazkilic,Lligadas,Ronda,Galià,Cádiz

, p. 101 - 110 (2015)

The synthesis and characterization of fully biobased ABA triblock copolyesters from PLA and castor oil derivatives are described. The synthetic strategy uses a dihydroxy telechelic polyester as a macroinitiator for the ring opening polymerization of l-lactide. This macroinitiator was obtained from a sulfur-containing hydroxyacid derivative of 10-undecenoic acid, which undergoes self-polycondensation with low amounts of biobased 1,4-butanediol, enables the obtention of two prepolymers of different weight. Two series of triblock copolyesters with different percentage of PLA contents were prepared and the resulting thioether-bearing copolyester oxidized to polysulfones. Both series of copolyesters showed improved thermal stability, decrease of crystallinity and a similar hydrophilicity with respect to the PLA homopolymer.

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