1606-80-0 Usage
General Description
AllylSulfonicAcid, also known as 2-Propen-1-sulfonic acid, is a colorless to pale yellow liquid with a pungent odor. It is a strong acid and is widely used in various industrial applications, including as a monomer in the production of polymers, as a co-monomer in the synthesis of ion exchange resins, and as a corrosion inhibitor in metal plating processes. AllylSulfonicAcid is also used as a catalyst in chemical reactions and as a stabilizer in the production of vinyl polymers. Additionally, it is utilized in the production of specialty chemicals and pharmaceuticals. Due to its corrosive and toxic nature, proper handling and storage of AllylSulfonicAcid are necessary to ensure safety.
Check Digit Verification of cas no
The CAS Registry Mumber 1606-80-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,0 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1606-80:
(6*1)+(5*6)+(4*0)+(3*6)+(2*8)+(1*0)=70
70 % 10 = 0
So 1606-80-0 is a valid CAS Registry Number.
1606-80-0Relevant articles and documents
Millburn,Venanzi
, p. 97,98, 100 (1968)
A general and efficient method for the preparation of organic sulfonic acids by insertion of sulfur trioxide into the metal-carbon bond of organolithiums
Smith, Keith,Hou, Duanjie
, p. 1530 - 1532 (2007/10/03)
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MECHANISTIC VARIATION IN ALKANESULFONYL CHLORIDE HYDROLYSIS AND RELATED REACTIONS
King, J. F.,Lam, J. Y. L.,Skonieczny, S.
, p. 177 - 180 (2007/10/02)
Kinetic and product ratio studies are consistent with the following mechanisms for the hydrolysis of methanesulfonyl chloride: (a) in acidic medium (pH 1-6) via a direct substitution on sulfur (SN2-S), (b) in mildly basic medium (pH 8-10) by way of sulfene (CH2=SO2) formation followed by trapping with water, and (c) in strongly basic solution (pH >10) via sulfene with trapping by the hydroxide ion.The reactions of primary and secondary alkanesulfonyl chlorides are qualitatively similar.
