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1H-Indole, 1-methyl-2,3-bis(methylthio)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

120517-34-2

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120517-34-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120517-34-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,5,1 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 120517-34:
(8*1)+(7*2)+(6*0)+(5*5)+(4*1)+(3*7)+(2*3)+(1*4)=82
82 % 10 = 2
So 120517-34-2 is a valid CAS Registry Number.

120517-34-2SDS

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-methyl-2,3-bis(methylthio)indole

1.2 Other means of identification

Product number -
Other names 1-methyl-2,3-dimethylthioindole

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:120517-34-2 SDS

120517-34-2Downstream Products

120517-34-2Relevant academic research and scientific papers

Acid-catalysed Isomerization of Indol-3-yl Sulphides to Indol-2-yl Sulphides: Unexpected Intermolecular Nature of the Rearrangement

Hamel, Pierre,Girard, Yves,Atkinson, Joseph G.

, p. 63 - 65 (1989)

The rearrangement of indol-3-yl sulphides (1) indol-2-yl sulphides (4), catalysed by proton acids, unexpectedly proceeds by an intermolecular mechanism involving initial disproportionation to an indole-2,3-diyl bis-sulphide (2) and an indole (3), followed by a reaction between (2) and (3) to yield the rearranged product (4).

Sulfenylation of Some Pyrroles and Indoles

Gilow, Helmuth M.,Brown, Christopher S.,Copeland, John N.,Kelly, Keith E.

, p. 1025 - 1034 (2007/10/02)

Methylsulfenylation of 1-substituted pyrroles and indoles was observed using 1-(methylthio)morpholine and an acid catalyst or with methylsulfenyl chloride and excess pyridine. 1-Substituents which are activating or weakly deactivating towards electrophili

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