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Benzenamine, N,N'-methanetetraylbis[4-bromo-] is a complex organic compound with the chemical formula C17H14Br4N2. It is a derivative of benzenamine, also known as aniline, which is a primary aromatic amine. Benzenamine, N,N'-methanetetraylbis[4-bromo- features a benzene ring with two amine groups (-NH2) attached to it. The unique aspect of this particular compound is the presence of four bromine atoms (Br) and a methanetetrayl group, which connects the two aniline units. The bromine atoms are attached to the benzene ring, and the methanetetrayl group acts as a linker between the two aniline molecules. This structure gives the compound specific properties that can be useful in various chemical applications, such as in the synthesis of dyes, pharmaceuticals, or as intermediates in organic chemistry. The compound's molecular weight is 634.91 g/mol, and it is likely to be a solid at room temperature. Due to the presence of multiple bromine atoms, it may also have significant halogenated properties, which can affect its reactivity and stability.

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  • 726-41-0 Structure
  • Basic information

    1. Product Name: Benzenamine, N,N'-methanetetraylbis[4-bromo-
    2. Synonyms:
    3. CAS NO:726-41-0
    4. Molecular Formula: C13H8Br2N2
    5. Molecular Weight: 352.028
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 726-41-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Benzenamine, N,N'-methanetetraylbis[4-bromo-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenamine, N,N'-methanetetraylbis[4-bromo-(726-41-0)
    11. EPA Substance Registry System: Benzenamine, N,N'-methanetetraylbis[4-bromo-(726-41-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 726-41-0(Hazardous Substances Data)

726-41-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 726-41-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,2 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 726-41:
(5*7)+(4*2)+(3*6)+(2*4)+(1*1)=70
70 % 10 = 0
So 726-41-0 is a valid CAS Registry Number.

726-41-0SDS

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 1,3-bis(p-bromophenyl)carbodiimide

1.2 Other means of identification

Product number -
Other names di(4-bromophenyl)carbodiimide

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:726-41-0 SDS

726-41-0Relevant articles and documents

CERAMIDE GALACTOSYLTRANSFERASE INHIBITORS FOR THE TREATMENT OF DISEASE

-

Paragraph 000703; 000705, (2018/01/17)

Described herein are compounds, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat or prevent diseases or disorders associated with the enzyme ceramide galactosyltransferase (CGT), such as, for example, lysosomal storage diseases. Examples of lysosomal storage diseases include, for example, Krabbe disease and Metachromatic Leukodystrophy.

Naphthyridine derivatives as a model system for potential lithium-sulfur energy-storage applications

Resch, Sebastian,Schneider, Anna-Rebekka,Beichler, Ronja,Spera, Marcelle B. M.,Fanous, Jean,Schollmeyer, Dieter,Waldvogel, Siegfried R.

supporting information, p. 933 - 937 (2015/02/19)

Naphthyridines have been identified as structural elements in sulfurized polyacrylonitrile, which is a common electrode material in lithium-sulfur batteries. Some dibenzonaphthyridine derivatives with a fused dithiolo moiety were prepared as model compounds for battery studies. These heterocyclic systems were prepared via the corresponding diphenyldicarbamide intermediate. Followed by naphthyridione formation, stepwise installation of the dithiolane subunit occurred in a straightforward manner. In the solid state, the heteroaromatic system is completely planar and was thoroughly characterized. Initial battery cycling tests indicated a potential use of such structural motifs in sulfur-lithium systems.

Manganese-catalyzed cleavage of a carbon-carbon single bond between carbonyl carbon and α-carbon atoms of ketones

Kuninobu, Yoichiro,Uesugi, Tadamasa,Kawata, Atsushi,Takai, Kazuhiko

supporting information; experimental part, p. 10406 - 10408 (2011/12/04)

Singled out: Treatment of ketones with carbodiimides in the presence of a catalytic amount of either [{HMn(CO)4}3] or [Mn 2(CO)10] gave amides in good to excellent yields. In this reaction, the carbon-carbon single bond of a ketone is cleaved efficiently. The reaction also proceeded by using isocyanates instead of carbodiimides. Copyright

O-Iodoxybenzoic acid mediated oxidative desulfurization of 1,3-disubstituted thioureas to carbodiimides

Chaudhari, Pramod S.,Dangate, Prasad S.,Akamanchi, Krishnacharya G.

supporting information; experimental part, p. 3065 - 3067 (2011/02/25)

An efficient and mild oxidative desulfurization procedure using o-iodoxybenzoic acid has been developed for the synthesis of carbodiimides starting from easily synthesizable 1,3-disubstituted thioureas.

A greener synthetic protocol for the preparation of carbodiimide

Ali, Abdur Rezzak,Ghosh, Harisadhan,Patel, Bhisma K.

experimental part, p. 1019 - 1021 (2010/04/02)

A new and facile preparation of symmetrical and unsymmetrical 1,3-diaryl and aryl-alkyl carbodiimides via a dehydrosulfurisation of their corresponding thioureas is described. Herein, the classical method of oxidative desulfurisation of thiourea to carbodiimide involving toxic heavy metal oxides (HgO) has been replaced with an easily available, cost-effective and environmentally benign reagent, iodine. Simple reaction conditions, easy purification of the products and high yields are important attributes of the present methodology and perhaps the best alternative from a green chemistry perspective. The only limitation to this method however, is in the preparation of 1,3-dialkyl substituted carbodiimide.

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