36247-34-4

Basic information

• Product Name: 1,12-Dodecanediol, bis(4-methylbenzenesulfonate)
• CAS NO: 36247-34-4
• Molecular Formula: C26H38O6S2
• Molecular Weight: 510.716
• Mol File: 36247-34-4.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 1,12-Dodecanediol, bis(4-methylbenzenesulfonate)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,12-Dodecanediol, bis(4-methylbenzenesulfonate)(36247-34-4)
• EPA Substance Registry System: 1,12-Dodecanediol, bis(4-methylbenzenesulfonate)(36247-34-4)

Safety Data

• Hazardous Substances Data: 36247-34-4(Hazardous Substances Data)

Upstream product

• 5675-51-4 1,12-dodecandiol 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 630-02-4 octacosane 
• 24772-65-4 1,12-diiodododecane 
• 1374336-11-4 C₃₄H₄₁N₃O₄S 
• 187977-47-5 Toluene-4-sulfonic acid 12-thiazolidin-3-yl-dodecyl ester 
• 73120-52-2 1,12-dimethoxydodecane 

Relevant articles and documents

Synthesis and recognition properties of calix[4]arene semitubes as ditopic hosts for: N -alkylpyridinium ion pairs

A series of calix[4]arene semitubes (4a-c) having alkyl bridging spacers of different lengths and flexibilities on their lower rim was synthesised and characterised in solution and in the solid state by 1H NMR spectroscopy and X-ray crystallogr

DNA Groove-binding Ability of Luminescent Platinum(II) Complexes based on a Family of Tridentate N^N^C Ligands Bearing Differently Substituted Alkyl Tethers

A family of luminescent PtII complexes is presented capable of binding DNA duplexes via groove binding. The complexes are based on a tridentate ligand with N^N^C donor functionality bearing a triazole, a pyridine and a phenyl entity. The triazole group is used to attach a series of pendant dodecane tethers with differently charged functional head groups (neutral hydroxyl group, anionic sulfate group, cationic tetraalkylammonium group). The DNA-binding behavior of the three resulting PtII complexes was characterized by UV/Vis, CD, and luminescence spectroscopy as well as viscosity measurements and computational docking studies. The data clearly indicate groove binding interactions for all three complexes. In addition, a light-switch effect was observed for the complexes upon the addition of DNA.

Immobilization of liposomes and vesicles on patterned surfaces by a peptide coiled-coil binding motif

Patchy surfaces: An azide-terminated self-assembled monolayer was patterned with the peptide sequence (EIAALEK)3 by using microcontact printing. This sequence forms stable coiled-coil heterodimers with the complementary peptide (KIAALKE)3