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Benzene, 1,1'-(1,2-ethynediyl)bis[3-nitro- is a complex organic compound with the chemical formula C14H8N2O4. It is a derivative of benzene, featuring two nitro groups attached to separate benzene rings, which are connected by an ethynediyl bridge. This molecule is characterized by its planar structure and the presence of a triple bond in the ethynediyl linker. The compound is known for its potential applications in the synthesis of various organic compounds and materials, such as dyes and pharmaceuticals, due to its unique structure and reactivity. However, it is also important to note that compounds containing nitro groups can be sensitive to heat and shock, requiring careful handling and storage.

2765-15-3

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2765-15-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2765-15-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,6 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2765-15:
(6*2)+(5*7)+(4*6)+(3*5)+(2*1)+(1*5)=93
93 % 10 = 3
So 2765-15-3 is a valid CAS Registry Number.

2765-15-3SDS

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 1-nitro-3-[2-(3-nitrophenyl)ethynyl]benzene

1.2 Other means of identification

Product number -
Other names 3,3'-Dinitro-tolan

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:2765-15-3 SDS

2765-15-3Relevant academic research and scientific papers

Direct Synthesis of Symmetric Diarylethynes from Calcium Carbide and Arylboronic Acids/Esters

Fu, Rugang,Li, Zheng

, p. 6648 - 6651 (2017/12/15)

A new methodology for the direct synthesis of symmetric diarylethynes from the reactions of calcium carbide with arylboronic acids/esters is described. Various symmetric diarylethynes were generated from the corresponding arylboronic acids/esters in satisfactory yield by using a palladium catalyst. The advantages of this protocol include the use of a readily available and easy-to-handle acetylene source, and a simple work-up procedure.

Palladium-Catalyzed Domino Process: Synthesis of Symmetrical Diarylalkynes, cis- and trans-Alkenes using Lithium Acetylide as a Synthon

Krishna, Jonnada,Krishna Reddy, Alavala Gopi,Satyanarayana, Gedu

, p. 3597 - 3610 (2016/01/25)

An efficient domino protocol has been developed for the synthesis of symmetrical diarylalkynes. Notably, the method was successful in the presence of a palladium catalyst without the support of a copper co-catalyst. Significantly, the method enabled the use of the commercially available and cheap lithium acetylide ethylenediamine complex as a source of acetylene for the construction of dual C-C bonds, with a wide range of compatibility towards various substituents of the aryl bromides/iodides. Significantly, this protocol was successfully applied to the synthesis of cis- and trans-alkenes in a highly stereoselective manner in a sequential one-pot process.

Pd-catalyzed [2+2+1] coupling of alkynes and arenes: Phenol diazonium salts as mechanistic trapdoors

Schmidt, Bernd,Berger, Rene,Kelling, Alexandra,Schilde, Uwe

supporting information; experimental part, p. 7032 - 7040 (2011/07/30)

Alkynes and phenol diazonium salts undergo a Pd-catalyzed [2+2+1] cyclization reaction to spiro[4,5]decatetraene-7-ones. This structure was confirmed for one example by X-ray single-crystal structure analysis. The reaction is believed to proceed through oxidative addition of the phenol diazonium cation to Pd0, subsequent insertion of two alkynes, followed by irreversible spirocyclization. Copyright

Oxidation of dihydrazones of diaryl α-diketones to diarylacetylenes using sodium periodate

Takale, Balaram S.,Telvekar, Vikas N.

supporting information; experimental part, p. 1279 - 1280 (2011/02/17)

Oxidation of dihydrazones of α-diketones to acetylene was investigated by using sodium periodate. Further, the described method is also found to be suitable for deprotection of monohydrazones of aldehydes and ketones. The process is mild, efficient, and applicable to both electron-withdrawing and -donating substituents to give good to excellent yields.

Oxidation of Aromatic Compounds. IV. Oxidation of Symmetrical Diarylacetylenes in the CF3COOH-CH2Cl2-PbO2 System. A New One-Pot Synthesis of 1,2,3,4-Tetraaryl-2-butene-1,4-diones

Rudenko, A. P.,Vasil'ev, A. V.

, p. 1360 - 1379 (2007/10/03)

Oxidation of symmetrical diarylacetylenes in the CF3COOH-CH2Cl2-PbO2 system (0-20 deg C, 1-3 h) yields 1,2,3,4-tetraaryl-2-butene-1,4-diones.According to (1)H NMR and GC-MS data the compounds synthesized have Z configuration.

Magnetic interaction between the triplet centers in ethynylenebis(phenylnitrenes) and 1,3-butadiyne-1,4-diylbis(phenylnitrenes)

Murata, Shigeru,Iwamura, Hiizu

, p. 5547 - 5556 (2007/10/02)

The magnetic interaction of the two triplet phenylnitrene units linked together through an acetylene or a diacetylene linkage has been investigated by ESR spectroscopy. Two regioisomeric (meta,para′ and meta, meta′) diazides of 1,2-diphenylacetylene 12a a

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