2,6-pyridinedicarboxamide
2,6-pyridinedicarboxamide structure
|
Common Name | 2,6-pyridinedicarboxamide | ||
|---|---|---|---|---|
| CAS Number | 4663-97-2 | Molecular Weight | 165.14900 | |
| Density | 1.375g/cm3 | Boiling Point | 479.5ºC at 760mmHg | |
| Molecular Formula | C7H7N3O2 | Melting Point | 317ºC (dec.)(lit.) | |
| MSDS | Chinese USA | Flash Point | 243.8ºC | |
| Symbol |
GHS07 |
Signal Word | Warning | |
| Name | Pyridine-2,6-dicarboxamide |
|---|---|
| Synonym | More Synonyms |
| Density | 1.375g/cm3 |
|---|---|
| Boiling Point | 479.5ºC at 760mmHg |
| Melting Point | 317ºC (dec.)(lit.) |
| Molecular Formula | C7H7N3O2 |
| Molecular Weight | 165.14900 |
| Flash Point | 243.8ºC |
| Exact Mass | 165.05400 |
| PSA | 99.07000 |
| LogP | 0.68000 |
| Index of Refraction | 1.621 |
| InChIKey | UUVCRNTVNKTNRK-UHFFFAOYSA-N |
| SMILES | NC(=O)c1cccc(C(N)=O)n1 |
| Symbol |
GHS07 |
|---|---|
| Signal Word | Warning |
| Hazard Statements | H315-H319-H335 |
| Precautionary Statements | P261-P305 + P351 + P338 |
| Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
| Hazard Codes | Xi: Irritant; |
| Risk Phrases | R36/37/38 |
| Safety Phrases | 26-36 |
| RIDADR | NONH for all modes of transport |
| HS Code | 2933399090 |
|
~72%
2,6-pyridinedic... CAS#:4663-97-2 |
| Literature: US2002/115860 A1, ; |
|
~94%
2,6-pyridinedic... CAS#:4663-97-2 |
| Literature: Helvetica Chimica Acta, , vol. 96, # 9 p. 1658 - 1669 |
|
~82%
2,6-pyridinedic... CAS#:4663-97-2 |
| Literature: Inorganica Chimica Acta, , vol. 363, # 6 p. 1092 - 1096 |
|
~82%
2,6-pyridinedic... CAS#:4663-97-2 |
| Literature: Pharmaceutical Chemistry Journal, , vol. 19, # 2 p. 126 - 129 Khimiko-Farmatsevticheskii Zhurnal, , vol. 19, # 2 p. 196 - 199 |
|
~%
2,6-pyridinedic... CAS#:4663-97-2 |
| Literature: Jahresbericht ueber die Fortschritte der Chemie und Verwandter Theile Anderer Wissenschaften, , p. 436 |
|
~%
2,6-pyridinedic... CAS#:4663-97-2 |
| Literature: Australian Journal of Chemistry, , vol. 44, # 8 p. 1041 - 1048 |
|
~%
2,6-pyridinedic... CAS#:4663-97-2 |
| Literature: Australian Journal of Chemistry, , vol. 44, # 8 p. 1041 - 1048 |
|
~%
2,6-pyridinedic... CAS#:4663-97-2 |
| Literature: Jahresbericht ueber die Fortschritte der Chemie und Verwandter Theile Anderer Wissenschaften, , p. 436 |
|
~%
2,6-pyridinedic... CAS#:4663-97-2 |
| Literature: Pharmaceutical Chemistry Journal, , vol. 19, # 2 p. 126 - 129 Khimiko-Farmatsevticheskii Zhurnal, , vol. 19, # 2 p. 196 - 199 |
| Precursor 8 | |
|---|---|
| DownStream 7 | |
CAS#:141-86-6
CAS#:33354-88-0
CAS#:138150-34-2
CAS#:84877-69-0![3,6,9,12,15,18,21-heptaoxa-27-azabicyclo[21.3.1]heptacosa-1(27),23,25-triene structure](https://image.chemsrc.com/caspic/189/86309-74-2.png)
CAS#:86309-74-2![3,6,9,12,15-pentaoxa-21-azabicyclo[15.3.1]henicosa-1(21),17,19-triene structure](https://image.chemsrc.com/caspic/448/53914-89-9.png)
CAS#:53914-89-9| HS Code | 2933399090 |
|---|---|
| Summary | 2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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Synthetic ion transporters can induce apoptosis by facilitating chloride anion transport into cells.
Nature Chemistry 6(10) , 885-92, (2014) Anion transporters based on small molecules have received attention as therapeutic agents because of their potential to disrupt cellular ion homeostasis. However, a direct correlation between a change... |
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Porphyrin-based switchable molecular turnstiles.
Chemistry 17(23) , 6443-52, (2011) The design, synthesis and structural characterisation, in solution, of two new molecular turnstiles based on Sn-porphyrin derivatives are described. The system is composed of a stator (5-(4-pyridyl)-1... |
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Solid state characterization of oligopyridine dicarboxamide helicates.
Chem. Commun. (Camb.) (8) , 924-5, (2004) A heptameric amide of 2,6-diaminopyridine and 2,6-pyridinedicarboxylic acid coordinates to Cu(II) to assemble into a double helical complex with a string of six shortly spaced Cu ions. |
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Name: Primary cell-based high-throughput screening assay for identification of compounds th...
Source: Johns Hopkins Ion Channel Center
Target: regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id: JHICC_RGS_Act_HTS
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Name: Luminescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id: OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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|
Name: QFRET-based biochemical primary high throughput screening assay to identify exosite i...
Source: The Scripps Research Institute Molecular Screening Center
Target: disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id: ADAM17_INH_QFRET_1536_1X%INH PRUN
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Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN
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Name: uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
Source: Burnham Center for Chemical Genomics
Target: N/A
External Id: BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
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Name: Binding affinity to G-quadruplex F21T DNA assessed as change in melting temperature a...
Source: ChEMBL
Target: Nucleic Acid
External Id: CHEMBL997244
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Name: Binding affinity to G-quadruplex F21T DNA assessed as change in melting temperature a...
Source: ChEMBL
Target: Nucleic Acid
External Id: CHEMBL997243
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Name: A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id: HMS979
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Name: High throughput fluorescence intensity-based biochemical assay to screen for small mo...
Source: University of Pittsburgh Molecular Library Screening Center
Target: furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id: MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
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Name: Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
Source: Broad Institute
Target: FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id: 2147-01_Inhibitor_SinglePoint_HTS_Activity
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| pyridine-2,6-dicarboxylic acid diamide |
| Pyridine dicarboxamide |
| 2,6-Pyridinedicarboxamide |
| Dipicolindiamide |
| pyridyl-2,6-dicarboxamide |
| dipicolinic acid diamide |
| MFCD00674100 |