925-89-3 Usage
General Description
(1E)-prop-1-ene-1-thiol, also known as 1-propenyl mercaptan, is a chemical compound with the formula C3H6S. It is a colorless liquid with a strong, unpleasant odor, similar to that of garlic or onions. (1E)-prop-1-ene-1-thiol is commonly used in the food industry as a flavoring agent and preservative due to its sulfurous aroma. Additionally, it is used in the production of rubber and plastics, as well as in the synthesis of other organic compounds. It is also found naturally in certain foods, such as onions, leeks, and garlic, contributing to their characteristic smell and taste. Furthermore, (1E)-prop-1-ene-1-thiol has potential applications in the pharmaceutical industry for the development of drugs and medical treatments. However, exposure to high concentrations of this compound can be irritating to the eyes, skin, and respiratory system, so proper handling and ventilation are necessary when working with it.
Check Digit Verification of cas no
The CAS Registry Mumber 925-89-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,2 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 925-89:
(5*9)+(4*2)+(3*5)+(2*8)+(1*9)=93
93 % 10 = 3
So 925-89-3 is a valid CAS Registry Number.
925-89-3Relevant articles and documents
Strausz et al.
, p. 717,720 (1965)
First synthesis and characterization of vinylselenols and vinyltellurols
Guillemin, Jean-Claude,Bouayad, Asmae,Vijaykumar, Dange
, p. 1163 - 1164 (2007/10/03)
Vinylselenols and vinyltellurols have been prepared by slow addition of tributyltin hydride to the corresponding divinyldiselenide or divinylditelluride in tetraglyme.
HIGH-TEMPERATURE ORGANIC SYNTHESIS XXXV. THERMAL REACTIONS OF DI(1-PROPENYL) SULFIDE
Ostroukhova, L. A.,Deryagina, E. N.,Korchevin, N. A.,Musorin, G. K.,Amosova, S. V.,Voronkov, M. G.
, p. 301 - 305 (2007/10/02)
The thermolysis of dipropenyl sulfide in a flow-type system in an atmosphere of nitrogen at 450-540 deg C leads to propenethiol, thiophene, methylthiophenes, and 2-ethylthiophene.The formation of the thiophene derivatives results from intramolecular radical cyclization of the initial sulfide.Dimethyl selenide (5-10 mole percent) substantially accelerates the thermolysis of dipropenyl sulfide, and the yield of 2-ethylthiophene at 450-480 deg C is increased appreciably.The high-temperature reactions of di(1-propenyl) sulfide with 2-halogenothiophenes and acetylene confirm that the propenethiol and thiophene derivatives are formed in parallel during the thermolysis of dipropenyl sulfide.