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Merck
CN

722987

2-Cyano-2-propyl benzodithioate

>97% (HPLC)

Synonym(s):

2-Cyanopropan-2-yl benzodithioate

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About This Item

Empirical Formula (Hill Notation):
C11H11NS2
CAS Number:
201611-85-0
Molecular Weight:
221.34
NACRES:
NA.23
PubChem Substance ID:
329763965
UNSPSC Code:
12352100
MDL number:
MFCD09037881

Key Documents

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Product Name

2-Cyano-2-propyl benzodithioate, >97% (HPLC)

InChI

1S/C11H11NS2/c1-11(2,8-12)14-10(13)9-6-4-3-5-7-9/h3-7H,1-2H3

SMILES string

CC(C)(SC(=S)c1ccccc1)C#N

InChI key

IDSLBLWCPSAZBL-UHFFFAOYSA-N

assay

>97% (HPLC)

form

solid or liquid

refractive index

n20/D 1.621

mp

28-31 °C

density

1.146 g/mL at 25 °C

storage temp.

2-8°C

Quality Level

100

Related Categories

Application

Reversible Addition Fragmentation Chain Transfer (RAFT) Polymerization
RAFT agent for controlled radical polymerization; especially suited for the polymerization of methacrylate and methacrylamide monomers. Chain Transfer Agent (CTA)

General description

Need help choosing the correct RAFT Agent? Please consult the RAFT Agent to Monomer compatibility table.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H317

Hazard Classifications

Skin Sens. 1

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

>230.0 °F - closed cup

flash_point_c

> 110 °C - closed cup

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Certificates of Analysis (COA)

Lot/Batch Number
MKCX4178
MKCV6195
MKCW3898
MKCT4216
MKCT6179

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Ryuichi Nakatani et al.
ACS applied materials & interfaces, 9(37), 31266-31278 (2017-03-18)
In this study, a series of perpendicular lamellae-forming poly(polyhedral oligomeric silsesquioxane methacrylate-block-2,2,2-trifluoroethyl methacrylate)s (PMAPOSS-b-PTFEMAs) was developed based on the bottom-up concept of creating a simple yet effective material by tailoring the chemical properties and molecular composition of the material. The
Xiaohan Zhang et al.
Langmuir : the ACS journal of surfaces and colloids, 34(27), 7998-8006 (2018-06-28)
Amphiphilic poly( N-(2-hydroxypropyl)methacrylamide) copolymers ( pHPMA) bearing cholesterol side groups in phosphate buffer saline self-assemble into nanoparticles (NPs) which can be used as tumor-targeted drug carriers. It was previously shown by us that human serum albumin (HSA) interacts weakly with
Yixiao Dong et al.
Acta biomaterialia, 108, 56-66 (2020-04-07)
Injury to the skin from severe burns can cause debilitating physical and psychosocial distress to the patients. Upon healing, deep dermal burns often result in devastating hypertrophic scar formation. For many decades, stem cell-based therapies have shown significant potential in
Laura Marcela Forero Ramirez et al.
Carbohydrate polymers, 224, 115153-115153 (2019-09-02)
A multi-reactive polysaccharide-based transurf (acting both as macro-Chain Transfer Agent and stabilizer) was used to confine RAFT polymerization of methyl methacrylate (MMA) at the oil/water (o/w) miniemulsion interface. Dithiobenzoate groups and hydrophobic aliphatic side chains were introduced onto dextran, conferring
Izumi Fukumoto et al.
PloS one, 8(11), e82540-e82540 (2013-12-07)
The immunostimulatory effects of the representative dental resin monomer 2-hydroxyethyl methacrylate (HEMA), a HEMA derivative that does not contain a double bond (2-hydroxyethyl isobutyrate, HEIB), and polymerized water-soluble oligomers of HEMA (PHEMA) were investigated. It is known that expression levels
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Articles

Protein- and Peptide- Polymer Conjugates by RAFT Polymerization

The modification of biomacromolecules, such as peptides and proteins, through the attachment of synthetic polymers has led to a new family of highly advanced biomaterials with enhanced properties.

RAFT Polymerization

RAFT polymerization offers living characteristics to radical polymerization, contributing versatility to reversible deactivation radical polymerization methods.

Functional Biomaterials Synthesized by Double-Head Polymerization Agents

Over the past two decades, the rapid advance of controlled living polymerization (CLP) techniques.

Micro Review of RAFT Polymerization

Micro review of reversible addition/fragmentation chain transfer (RAFT) polymerization.

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Protocols

Concepts and Tools for RAFT Polymerization

We present an article about RAFT, or Reversible Addition/Fragmentation Chain Transfer, which is a form of living radical polymerization.

RAFT Polymerization Procedures

RAFT polymerization offers precise control, enabling tailored synthesis of complex polymer structures.

Polymerizing via ATRP

Polymerization via ATRP procedures demonstrated by Prof. Dave Haddleton's research group at the University of Warwick.

Typical Procedures for Polymerizing via RAFT

We presents an article featuring procedures that describe polymerization of methyl methacrylate and vinyl acetate homopolymers and a block copolymer as performed by researchers at CSIRO.

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