872-10-6 Usage
General Description
A yellow colored liquid with an obnoxious odor. Less dense than water and slightly soluble in water. Flash point 185°F. May irritate skin, eyes and mucous membranes. May decompose to toxic oxides of sulfur when heated to high temperatures. Used to make other chemicals.
Air & Water Reactions
Slightly soluble in water.
Reactivity Profile
Organosulfides, such as N-AMYL SULFIDE, are incompatible with acids, diazo and azo compounds, halocarbons, isocyanates, aldehydes, alkali metals, nitrides, hydrides, and other strong reducing agents. Reactions with these materials generate heat and in many cases hydrogen gas. Many of these compounds may liberate hydrogen sulfide upon decomposition or reaction with an acid.
Health Hazard
Inhalation or contact with material may irritate or burn skin and eyes. Fire may produce irritating, corrosive and/or toxic gases. Vapors may cause dizziness or suffocation. Runoff from fire control or dilution water may cause pollution.
Check Digit Verification of cas no
The CAS Registry Mumber 872-10-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,7 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 872-10:
(5*8)+(4*7)+(3*2)+(2*1)+(1*0)=76
76 % 10 = 6
So 872-10-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H22S/c1-3-5-7-9-11-10-8-6-4-2/h3-10H2,1-2H3
872-10-6Relevant articles and documents
Electrochemical synthesis of organochalcogenides in aqueous medium
Ribeiro Neto, Pedro B.,Santana, Sonydelane O.,Levitre, Guillaume,Galdino, Danilo,Oliveira, Jadson L.,Ribeiro, Rogério T.,Barros, Maria E. S. B.,Bieber, Lothar W.,Menezes, Paulo H.,Navarro, Marcelo
supporting information, p. 657 - 661 (2016/02/12)
The electrochemical preparation of telluride, selenide and sulfide ions was carried out in NaOH aqueous solution, using a two compartment cell. Organochalcogenides were prepared from halogenated compounds in a two-step procedure. The monochalcogenides were obtained as the major products in good yields.
CHEMISTRY OF A MOLYBDENUM-PERSULFIDE COMPLEX: ALKYLATION AND OXIDATIVE COUPLING
Harpp, David N.,MacDonald, J. Gavin
, p. 703 - 706 (2007/10/02)
The reaction of alkyl halides, sulfinyl and sulfonyl chlorides with (NH4)2 has been found to afford sulfides and disulfides in good-excellent yield.The effect of solvent polarity and reaction time is discussed.
Synthetic Methods and Reactions; 80. Deoxygenation of Sulfoxides with Cyanuric Chloride and Fluoride
Olah, George A.,Fung, Alexander P.,Gupta, B.G. Balaram,Narang, Subhash C.
, p. 221 (2007/10/02)
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