10595-09-2 Usage
Description
3,3'-Thiodipropanol, also known as 3,3'-thiobis(1-propanol), is an organic compound with the chemical formula C?H??OS. It is a clear, colorless to yellow liquid at room temperature and is characterized by the presence of a thiol (-SH) group and two hydroxyl (-OH) groups attached to a propane chain. This unique structure endows 3,3'-thiodipropanol with specific chemical properties and potential applications in various industries.
Uses
Used in Analytical Chemistry:
3,3'-Thiodipropanol is used as a reagent for the detection and determination of thiodiglycol in water samples. Thiodiglycol is a common contaminant in industrial processes and can be toxic to aquatic life and the environment. The presence of 3,3'-thiodipropanol allows for the accurate identification and quantification of thiodiglycol, enabling better monitoring and control of this pollutant.
Used in Pharmaceutical Industry:
3,3'-Thiodipropanol can be utilized as a building block or intermediate in the synthesis of various pharmaceutical compounds. Its unique structure, with both thiol and hydroxyl functional groups, makes it a versatile starting material for the development of new drugs with potential therapeutic applications.
Used in Chemical Synthesis:
Due to its distinct chemical properties, 3,3'-thiodipropanol can be employed as a reactant in the synthesis of a wide range of organic compounds. Its thiol and hydroxyl groups can participate in various chemical reactions, such as oxidation, substitution, and condensation, leading to the formation of new molecules with diverse applications in different industries.
Used in Research and Development:
3,3'-Thiodipropanol can serve as a valuable research tool in the field of organic chemistry, particularly in the study of thiol-containing compounds and their reactivity. Its unique structure allows researchers to explore new reaction pathways and develop innovative synthetic strategies for the preparation of complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 10595-09-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,9 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10595-09:
(7*1)+(6*0)+(5*5)+(4*9)+(3*5)+(2*0)+(1*9)=92
92 % 10 = 2
So 10595-09-2 is a valid CAS Registry Number.
10595-09-2Relevant articles and documents
THE SYNTHESIS AND PROPERTIES OF ANTIMONY-SULPHUR AND ANTIMONY-OXYGEN LIGANDS
Levason, William,Sheikh, Baharuddin
, p. 1 - 10 (1981)
The synthesis and properties of a series of potentially bi-, tri- and tetra-dentate ligands containing various combinations of antimony and sulphur and antimony and oxygen donors, is described.Included are SbPhn(o-C6H4OMe)3-n (n = 0, 1, 2); SbMe2(o-C6H4OMe); SbPhn(o-C6H4SMe3)3-n (n = 0, 1, 2); SbMe2(o-C6H4SMe); MeS(CH2)3SbR2 (R = Me, Ph) and S(CH2CH2CH2SbPh2)2.Attempts to prepare ligands with dimethylene backbones including (R2SbCH2CH2)2S (R = Me, Ph) failed.The ligands were characterised by analysis, 1H NMR and mass spectra, and by the preparation of quaternary derivatives.
Intramolecular sulfur-assisted NaBH4 reduction of esters synthesis of 5-oxo-ETE and 5-oxo-12-HETE
Khanapure, Subhash P.,Saha, Goutam,Sivendran, Sashikala,Powell, William S.,Rokach, Joshua
, p. 5653 - 5657 (2000)
Ester groups are reduced very efficiently in sulfur-containing molecules situated at close proximity to the ester group. We have used this procedure to regioselectively, efficiently and in high yield reduce an ester group in the presence of another ester group further removed from the sulfur atom. (C) 2000 Elsevier Science Ltd.
Sulfoboration of Cyclic Ethers - A Preparative Route to Mercaptoalkanols and Bis(hydroxyalkyl) Sulfides
Koester, Roland,Kucznierz, Ralf
, p. 835 - 842 (2007/10/02)
Bis(1,5-cyclooctanediylboryl) sulfide (1) reacts slowly with the cyclic ethers A-D to give O,S-bis(9-BBN)mercaptoalkanols 2a-d in excellent yields.From oxetane (E) and 1, however, 2e is obtained rapidly, which further reacts with E to yield the bis(9-BBN-oxypropyl) sulfide 3ee. 2a and c react with E to form the mixed thioethers 3ae and 3ce, respectively.The methanolysis of 2a-e leads to the O-(9-BBN)mercaptoalkanols 4a-e.The compounds 2 and 3 react with acetylacetone or with 2-aminoethanol to yield the mercaptoalkanols 7a-c, e and the bis(hydroxyalkyl) sulfides 8ae, 8ce and 8ee, resp., in high yields beside the 9-BBN-chelates 5 or 6.Key Words: Ethers, cyclic, cleavage of / Sulfoborations / Mercaptoethanols, 9-BBN derivatives of / Sulfides, bis(hydroxyalkyl), 9-BBN derivatives of