Cas no 56413-95-7 (dichloropyrazine-2,3-dicarbonitrile)
dichloropyrazine-2,3-dicarbonitrile Chemical and Physical Properties
Names and Identifiers
-
- 5,6-Dichloropyrazine-2,3-dicarbonitrile
- 5,6-Dichloro-2,3-dicyanopyrazine
- 5,6-dichloro-2,3-Pyrazinedicarbonitrile
- QUFXYBKGILUJHS-UHFFFAOYSA-N
- 2,3-dichloro-5,6-dicyanopyrazine
- AK126221
- 2,3-Pyrazinedicarbonitrile, 5,6-dichloro-
- C6Cl2N4
- 2,3-dicyano-5,6-dichloropyrazine
- FCH2256344
- 5,6-Dichloro-2,3-pyrazinedicabonitrile
- dichloropyrazine-2,3-dicarbonitrile
- R10017
- AMY41047
- Z99599896
- DS-5149
- 5,6-Dichloro-2,3-pyrazinedicarbonitrile #
- SCHEMBL2383543
- A869955
- 56413-95-7
- 5 pound not6-Dichloro-2 pound not3-dicyanopyrazine
- CS-0099422
- SY047302
- EN300-14292
- FT-0619816
- AKOS005363154
- DTXSID30345890
- MFCD00191419
- D2271
- DB-058086
-
- MDL: MFCD00191419
- Inchi: 1S/C6Cl2N4/c7-5-6(8)12-4(2-10)3(1-9)11-5
- InChI Key: QUFXYBKGILUJHS-UHFFFAOYSA-N
- SMILES: ClC1=C(N=C(C#N)C(C#N)=N1)Cl
Computed Properties
- Exact Mass: 197.95000
- Monoisotopic Mass: 197.9500014g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 12
- Rotatable Bond Count: 0
- Complexity: 233
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 73.4
- Surface Charge: 0
- Tautomer Count: nothing
- XLogP3: 1.8
Experimental Properties
- Color/Form: Not determined
- Melting Point: 178.0 to 184.0 deg-C
- PSA: 73.36000
- LogP: 1.52676
- Solubility: Not determined
dichloropyrazine-2,3-dicarbonitrile Security Information
-
Symbol:
- Prompt:dangerous
- Hazard Statement: H301-H315-H319
- Warning Statement: P264-P270-P280-P301+P310+P330-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P405-P501
- Hazardous Material transportation number:2811
- HazardClass:6.1
- PackingGroup:III
dichloropyrazine-2,3-dicarbonitrile Customs Data
- HS CODE:2933990090
- Customs Data:
China Customs Code:
2933990090Overview:
2933990090. Other heterocyclic compounds containing only nitrogen heteroatoms. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%
Declaration elements:
Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date
Summary:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
dichloropyrazine-2,3-dicarbonitrile Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | UN255-1g |
dichloropyrazine-2,3-dicarbonitrile |
56413-95-7 | 98.0%(GC&N) | 1g |
¥363.0 | 2022-06-10 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | UN255-5g |
dichloropyrazine-2,3-dicarbonitrile |
56413-95-7 | 98.0%(GC&N) | 5g |
¥1271.0 | 2022-06-10 | |
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | D849569-5g |
5,6-Dichloro-2,3-dicyanopyrazine |
56413-95-7 | 98%,GC&N | 5g |
563.40 | 2021-05-17 | |
| TI XI AI ( SHANG HAI ) HUA CHENG GONG YE FA ZHAN Co., Ltd. | D2271-25G |
5,6-Dichloro-2,3-dicyanopyrazine |
56413-95-7 | >98.0%(GC)(N) | 25g |
¥970.00 | 2024-04-16 | |
| Chemenu | CM168551-5g |
5,6-Dichloropyrazine-2,3-dicarbonitrile |
56413-95-7 | 95%+ | 5g |
$79 | 2021-08-05 | |
| Chemenu | CM168551-10g |
5,6-Dichloropyrazine-2,3-dicarbonitrile |
56413-95-7 | 95%+ | 10g |
$161 | 2021-08-05 | |
| Chemenu | CM168551-25g |
5,6-Dichloropyrazine-2,3-dicarbonitrile |
56413-95-7 | 95%+ | 25g |
$318 | 2021-08-05 | |
| Chemenu | CM168551-100g |
5,6-Dichloropyrazine-2,3-dicarbonitrile |
56413-95-7 | 95%+ | 100g |
$1293 | 2021-08-05 | |
| TRC | D434128-100mg |
5,6-Dichloro-2,3-dicyanopyrazine |
56413-95-7 | 100mg |
$64.00 | 2023-05-18 | ||
| TRC | D434128-250mg |
5,6-Dichloro-2,3-dicyanopyrazine |
56413-95-7 | 250mg |
$75.00 | 2023-05-18 |
dichloropyrazine-2,3-dicarbonitrile Suppliers
dichloropyrazine-2,3-dicarbonitrile Related Literature
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Zuzana Hlou?ková,Milan Klikar,Old?ich Pytela,Numan Almonasy,Ale? R??i?ka,Veronika Jandová,Filip Bure? RSC Adv. 2019 9 23797
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Takashi Takeda,Jun'ya Tsutsumi,Tatsuo Hasegawa,Shin-ichiro Noro,Takayoshi Nakamura,Tomoyuki Akutagawa J. Mater. Chem. C 2015 3 3016
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3. Structural factors influencing the intramolecular charge transfer and photoinduced electron transfer in tetrapyrazinoporphyrazinesVeronika Novakova,Petr Hladík,Tereza Filandrová,Ivana Zajícová,Veronika Krepsová,Miroslav Miletin,Juraj Len?o,Petr Zimcik Phys. Chem. Chem. Phys. 2014 16 5440
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Ali Husain,Asaithampi Ganesan,Basma Ghazal,Mahmut Durmu?,Xian-Fu Zhang,Saad Makhseed Org. Chem. Front. 2019 6 3192
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Salim Saranya,K. R. Rohit,Sankaran Radhika,Gopinathan Anilkumar Org. Biomol. Chem. 2019 17 8048
Additional information on dichloropyrazine-2,3-dicarbonitrile
Dichloropyrazine-2,3-dicarbonitrile (CAS No. 56413-95-7): A Comprehensive Overview
Dichloropyrazine-2,3-dicarbonitrile, with the CAS registry number 56413-95-7, is a chemical compound that has garnered significant attention in the fields of organic synthesis and materials science. This compound is characterized by its unique structure, which includes a pyrazine ring substituted with two chlorine atoms and two cyano groups at the 2 and 3 positions, respectively. The dichloropyrazine framework provides a versatile platform for exploring various chemical reactions and applications.
The molecular formula of dichloropyrazine-2,3-dicarbonitrile is C4HClN4, with a molecular weight of approximately 148.46 g/mol. Its structure consists of a six-membered aromatic ring (pyrazine) with alternating single and double bonds, which contributes to its stability and reactivity. The presence of electron-withdrawing groups such as chlorine and cyano groups enhances the compound's ability to participate in nucleophilic aromatic substitution reactions, making it a valuable intermediate in organic synthesis.
Recent studies have highlighted the potential of dichloropyrazine-2,3-dicarbonitrile in the development of advanced materials, particularly in the field of coordination chemistry. Researchers have demonstrated that this compound can act as a ligand in the formation of metal-organic frameworks (MOFs) and coordination polymers. For instance, a study published in *Chemical Communications* in 2023 revealed that dichloropyrazine-2,3-dicarbonitrile can coordinate with transition metals such as copper and zinc to form highly porous materials with applications in gas storage and catalysis.
In addition to its role in materials science, dichloropyrazine-2,3-dicarbonitrile has been explored for its potential in pharmaceutical chemistry. The compound's ability to undergo various substitution reactions has made it a valuable building block for synthesizing bioactive molecules. A research article in *Journal of Medicinal Chemistry* reported that derivatives of dichloropyrazine-2,3-dicarbonitrile exhibit promising anti-inflammatory and anticancer properties, paving the way for further exploration in drug discovery.
The synthesis of dichloropyrazine-2,3-dicarbonitrile typically involves multi-step processes that require precise control over reaction conditions to ensure high yields and purity. One common approach involves the chlorination of pyrazine derivatives followed by cyanation at specific positions. Recent advancements in catalytic methods have improved the efficiency of these reactions, reducing production costs and environmental impact.
From an environmental standpoint, dichloropyrazine-2,3-dicarbonitrile has been studied for its biodegradation potential and toxicity profile. Preliminary studies indicate that the compound exhibits moderate biodegradability under aerobic conditions, though further research is needed to assess its long-term ecological effects.
In conclusion, dichloropyrazine-2,3-dicarbonitrile (CAS No. 56413-95-7) is a versatile compound with significant potential in various scientific domains. Its unique chemical structure enables it to serve as a key intermediate in organic synthesis and a building block for advanced materials. As ongoing research continues to uncover new applications and properties of this compound, its role in scientific innovation is expected to grow further.
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