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Selenourea, N-methyl-N-phenyl-, also known as N-Methyl-N-phenylselenourea or MPSO, is an organic compound with the chemical formula C8H10N2Se. It is a derivative of selenourea, which is a compound containing a selenocarbonyl group (C=Se) and two amino groups (NH2). In N-methyl-N-phenylselenourea, one of the amino groups is replaced by a methyl group (CH3), and the other is replaced by a phenyl group (C6H5). Selenourea, N-methyl-N-phenyl- is a white crystalline solid and is used as a reagent in organic synthesis, particularly in the preparation of various seleno-organic compounds. It is also known for its potential applications in the field of cancer research due to its ability to inhibit certain enzymes involved in cancer cell growth.

6124-04-5

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6124-04-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6124-04-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,2 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6124-04:
(6*6)+(5*1)+(4*2)+(3*4)+(2*0)+(1*4)=65
65 % 10 = 5
So 6124-04-5 is a valid CAS Registry Number.

6124-04-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-1-phenyl-selenourea

1.2 Other means of identification

Product number -
Other names 1-Methyl-1-phenyl-selenourea

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:6124-04-5 SDS

6124-04-5Downstream Products

6124-04-5Relevant academic research and scientific papers

Preparation and characterisation of N,N-disubstituted 2-amino-selenazoles

Keil, Dietmar,Hartmann, Horst

, p. 169 - 184 (2007/10/03)

As a result of checking suited methods for preparing N,N-disubstituted 2-amino-selenazoles 14 as a nearly unknown class of highly reactive selenazoles a simple route starting from N,N-disubstituted selenoureas 12 has been elaborated and used for the synthesis of a series of these compounds. The necessary selenium-containing starting compounds 12 are available from N,N-disubstituted cyanamides 18 and hydrogen selenide.

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