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Benzenecarbodithioic acid, 1-methyl-2-oxo-2-[[4-(9-phenanthrenyl)butyl]amino]ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

918155-49-4

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918155-49-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 918155-49-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,8,1,5 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 918155-49:
(8*9)+(7*1)+(6*8)+(5*1)+(4*5)+(3*5)+(2*4)+(1*9)=184
184 % 10 = 4
So 918155-49-4 is a valid CAS Registry Number.

918155-49-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name PBTP

1.2 Other means of identification

Product number -
Other names N-[4-(9-phenanthrenyl)butyl-2-(2-phenyl-1-thioxo)thio]-propanamide

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:918155-49-4 SDS

918155-49-4Downstream Products

918155-49-4Relevant academic research and scientific papers

RAFT polymerization and self-assembly of thermoresponsive poly(N-decylacrylamide-b-N,N-diethylacrylamide) block copolymers bearing a phenanthrene fluorescent α-end group

Prazeres, Telmo J.V.,Beija, Mariana,Charreyre, Marie-Thérèse,Farinha, José Paulo S.,Martinho, José M.G.

experimental part, p. 355 - 367 (2011/02/24)

Phenanthrene α-end-labeled poly(N-decylacrylamide-b-N,N-diethylacrylamide) (PDcAn-b-PDEAm) block copolymers consisting in a highly hydrophobic block (n = 11) and a thermoresponsive block with variable length (79 ≤ m ≤ 468) were synthesized by reversible addition-fragmentation chain transfer (RAFT) polymerization. A new phenanthrene-labeled chain transfer agent (CTA) was synthesized and used to control the RAFT polymerization of a hydrophobic acrylamide derivative, N-decylacrylamide (DcA). This first block was further used as macroCTA to polymerize N,N-diethylacrylamide (DEA) in order to prepare diblock copolymers with the same hydrophobic block of PDcA (number average molecular weight: Mn = 2720 g mol-1, polydispersity index: Mw/Mn = 1.13) and various PDEA blocks of several lengths (Mn = 10,000-60,000 g mol-1) with a very high blocking efficiency. The resulting copolymers self-assemble in water forming thermoresponsive micelles. The critical micelle concentration (CMC) was determined using Fo?rster resonance energy transfer (FRET) between phenanthrene linked at the end of the PDcA block and anthracene added to the solution at a low concentration (10-5 M), based on the fact that energy transfer only occurs when phenanthrene and anthracene are located in the core of the micelle. The CMC (~2 μM) was obtained at the polymer concentration where the anthracene fluorescence intensity starts to increase. The size of the polymer micelles decreases with temperature increase around the lower critical solution temperature of PDEA in water (LCST ~ 32 °C) owing to the thermoresponsiveness of the PDEA shell.

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