1035959-94-4

Basic information

• Product Name: S,S,S-[2,2,2-(1,2,4-cyclohexanetriyl)triethyl]tristhioacetate
• Synonyms: S,S,S-[2,2,2-(1,2,4-cyclohexanetriyl)triethyl]tristhioacetate
• CAS NO: 1035959-94-4
• Molecular Weight: 390.632
• Mol File: 1035959-94-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: S,S,S-[2,2,2-(1,2,4-cyclohexanetriyl)triethyl]tristhioacetate(CAS DataBase Reference)
• NIST Chemistry Reference: S,S,S-[2,2,2-(1,2,4-cyclohexanetriyl)triethyl]tristhioacetate(1035959-94-4)
• EPA Substance Registry System: S,S,S-[2,2,2-(1,2,4-cyclohexanetriyl)triethyl]tristhioacetate(1035959-94-4)

Safety Data

• Hazardous Substances Data: 1035959-94-4(Hazardous Substances Data)

Upstream product

• 2855-27-8 1.2.4- trivinylcyclohexane 
• 507-09-5 tiolacetic acid 

Downstream Products

• 25664-92-0 1,2,4-tris(2-mercaptoethyl)cyclohexane 
• 1225201-62-6 1,2,4-tris-(3-chloro-3-thia-propyl)cyclohexane 

Relevant articles and documents

Covalent Adaptable Networks with Tunable Exchange Rates Based on Reversible Thiol–yne Cross-Linking

The design of covalent adaptable networks (CANs) relies on the ability to trigger the rearrangement of bonds within a polymer network. Simple activated alkynes are now used as versatile reversible cross-linkers for thiols. The click-like thiol–yne cross-linking reaction readily enables network synthesis from polythiols through a double Michael addition with a reversible and tunable second addition step. The resulting thioacetal cross-linking moieties are robust but dynamic linkages. A series of different activated alkynes have been synthesized and systematically probed for their ability to produce dynamic thioacetal linkages, both in kinetic studies of small molecule models, as well as in stress relaxation and creep measurements on thiol–yne-based CANs. The results are further rationalized by DFT calculations, showing that the bond exchange rates can be significantly influenced by the choice of the activated alkyne cross-linker.

THIOCARBAMOYLDISULFANYL-FUNCTIONAL CYCLOALIPHATIC COMPOUND, PROCESS FOR ITS PREPARATION, FILLED SULFUR-VULCANIZABLE ELASTOMER COMPOSITION CONTAINING SAME AND ARTICLES FABRICATED THEREFROM

A thiocarbamoyldisulfanyl-functional cycloaliphatic compound, useful as a crosslinker for filled sulfur-vulcanizable elastomer compositions, is represented by the general formula: G[-CaH2a-S-S-C(=S)NR2]n wherein G is a saturated, monocyclic aliphatic group of valence n containing from 5 to 12 carbon atoms and optionally containing at least one halogen or a saturated monocyclic silicone [RSiO-]n [R2SiO-]p group of valence n; each R independently is a hydrogen or a monovalent hydrocarbon of up to 20 carbon atoms; each occurrence of subscripts a independently is an integer wherein a is 2 to 6; n is an integer of from 3 to 6; and, p is an integer of from 0 to 3.