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1H-Imidazole, 2,4,5-tris(methylthio)-1-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106848-40-2

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106848-40-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106848-40-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,8,4 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 106848-40:
(8*1)+(7*0)+(6*6)+(5*8)+(4*4)+(3*8)+(2*4)+(1*0)=132
132 % 10 = 2
So 106848-40-2 is a valid CAS Registry Number.

106848-40-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-2,4,5-tris(methylsulfanyl)imidazole

1.2 Other means of identification

Product number -
Other names -

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:106848-40-2 SDS

106848-40-2Downstream Products

106848-40-2Relevant academic research and scientific papers

Azoles. Part 6. A Convenient Synthesis of Polysubstituted Imidazoles from 1-Protected 2,4,5-Tribromoimidazoles

Iddon, Brian,Khan, Nazir

, p. 1453 - 1456 (2007/10/02)

Starting from 1-benzyl-2,4,5-tribromoimidazole 'one-pot' methods are described for the synthesis of 1-benzyl-4,5-dibromo-2-methylthioimidazole (1) (72percent), 1-benzyl-4-bromo-2,5-bis(methylthio)imidazole (3) (72percent), 1-benzyl-2,4,5-tris(methylthio)i

A CONVENIENT SYNTHESIS OF 4(5)-MONO-, 4,5-DI-, AND 2,4,5-TRI-SUBSTITUTED IMIDAZOLES

Iddon, Brian,Khan, Nazir

, p. 1635 - 1638 (2007/10/02)

A procedure is described for the stepwise introduction of substituents (hydrogen included) into the imidazole ring by FGI of the bromine atoms in 1-protected 2,4,5-tribromo-imidazoles in the order 2-5-4 using halogen-metal exchange techniques.

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