137669-00-2 Usage
Synthesized from
Reaction between 1,2-Benzenediol, 3-methoxyand 4-methylbenzenesulfonyl chloride
Common Uses
Phenolic and antioxidant in cosmetics and personal care products
Found in
Hair dyes, anti-aging creams, and skincare products
Function
Neutralizes free radicals and prevents oxidation of other ingredients
Potential Risks
Prolonged exposure or high concentrations may cause skin irritation and allergic reactions in sensitive individuals
Precaution
Use products containing 1,2-Benzenediol, 3-methoxy-, bis(4-methylbenzenesulfonate) with caution and in accordance with recommended usage instructions
Check Digit Verification of cas no
The CAS Registry Mumber 137669-00-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,6,6 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 137669-00:
(8*1)+(7*3)+(6*7)+(5*6)+(4*6)+(3*9)+(2*0)+(1*0)=152
152 % 10 = 2
So 137669-00-2 is a valid CAS Registry Number.
137669-00-2Relevant academic research and scientific papers
Civitello, Edgar R.,Rapoport, Henry
, p. 834 - 840 (1992)
The electrochemical reductions of eight bis(tosyloxy)benzenoid compounds were studied as a method for the regioselective cleavage of aryl tosylates.For the methyl bis(tosyloxy)benzoate isomers, a strong preference was observed for cleavage of the tosyl group in conjugation with the electron-withdrawing ester moiety.Thus it was possible to selectively cleave tosyl groups to the ortho or para positions over tosyl groups at the meta positions.The bis(tosyloxy)anisole isomers displayed the opposite regioselectivity favoring cleavage of tosyl groups that were meta to the electron-donating methoxy substituent.The general electrochemical process for the reduction of aryl tosylates has been shown to be selective, high yielding, and reproducible on gram quantities.
