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120107-25-7

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120107-25-7 Usage

Type of compound

Diamine

Structure

Contains amine groups (-NH2) attached to two carbon atoms

Usage

a. Organic synthesis
b. Pharmaceutical research (building block for complex molecules)
c. Corrosion inhibitor
d. Component in production of dyes, surfactants, and polymers
e. Potential applications in medicine and biotechnology

Safety

Handle with care and follow safety protocols due to potential toxic and hazardous nature

Check Digit Verification of cas no

The CAS Registry Mumber 120107-25-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,1,0 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 120107-25:
(8*1)+(7*2)+(6*0)+(5*1)+(4*0)+(3*7)+(2*2)+(1*5)=57
57 % 10 = 7
So 120107-25-7 is a valid CAS Registry Number.

120107-25-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methyl-N'-(2-methylphenyl)ethane-1,2-diamine

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:120107-25-7 SDS

120107-25-7Relevant articles and documents

Synthesis and study of 1-aryl-1H-4,5-dihydroimidazoles

Perillo, Isabel,Caterina, M. Cristina,Lopez, Julieta,Salerno, Alejandra

, p. 851 - 856 (2007/10/03)

An easy synthesis of 1-aryl-1H-4,5-dihydroimidazoles 1 by cyclocondensation of N-aryl-N′-formylethylenediamines 2 is described. Such precursors were synthesized by selective formylation of N-arylethylenediamines 3 with p-nitrophenyl formate. Cyclizations were performed using trimethylsilyl polyphosphate. Chemical properties of compounds 1, typical of amidine system, were studied. Reaction of 1 with methyl iodide leads to the corresponding 1-aryl-3-methyl-1H-4,5-dihydroimidazolium salts 5. Reduction of dihydroimidazoles 1 with sodium cyanoborohydride provides a convenient access to N-aryl-N′-methylethylenediamines 4.

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