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53394-81-3

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53394-81-3 Usage

Usage

Dietary supplement to reduce inflammation and pain

Natural occurrence

Found in some plants and animals

Production

Also produced synthetically for commercial use

Sulfur content

Source of sulfur, important for collagen formation in the body

Potential benefits

Studied for treating arthritis, allergies, and skin conditions

Research status

More research needed to fully understand effects on human health

Safety considerations

Potential allergic reactions and interactions with certain medications

Check Digit Verification of cas no

The CAS Registry Mumber 53394-81-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,9 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 53394-81:
(7*5)+(6*3)+(5*3)+(4*9)+(3*4)+(2*8)+(1*1)=133
133 % 10 = 3
So 53394-81-3 is a valid CAS Registry Number.

53394-81-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-4-methylsulfinylbutane

1.2 Other means of identification

Product number -
Other names Butane,1-chloro-4-(methylsulfinyl)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:53394-81-3 SDS

53394-81-3Downstream Products

53394-81-3Relevant articles and documents

ANODIC OXIDATION OF 1,n-HALO(ALKYLTHIO)ALKANES AND 1,n-CHLORO(ALKYLSULFINYL)ALKANES

Aced, Ahmed,Anklam, Elke,Asmus, Klaus-Dieter,Pohl, Klaus,Glass, Richard S.,et al.

, p. 53 - 62 (2007/10/02)

Anodic oxidation of 1,n-halo(alkylthio)alkanes n-S-R, X=Cl, Br, I> and 1,n-halo(alkylsulfinyl)alkanes n-S(O)-R> was studied by cyclic voltammetry in anhydrous acetonitrile and by controlled potential electrolyses.The ease of sulfur oxidation was not affected by the alkyl substituents R or the number of methylene groups n in compounds with n>2.The oxidation of the 1,2-halo(alkylthio)ethanes (n=2) occurred at slightly higher potentials.The peak potentials decreased slightly in the order Cl>Br>I which is probably due to the electronegativity of the halogen atoms.The investigated anodic oxidation was shown to be a two electron irreversible process.Electrolyses in aqueous acetonitrile led to the corresponding sulfoxides and sulfones in good yields.

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