- 3-Nitrophthalonitrile
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- $65.60
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2026-08-11
- CAS:51762-67-5
- Min. Order: 25Kg/Drum
- Purity: 99.5%HPLC
- Supply Ability: 10tons/month
- 3-Nitrophthalonitrile
-
- $10.70
-
2026-05-28
- CAS:51762-67-5
- Min. Order: 10kg
- Purity: 99%
- Supply Ability: 10000kg
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| | 3-Nitrophthalonitrile Basic information |
| | 3-Nitrophthalonitrile Chemical Properties |
| Melting point | 162-165 °C (lit.) | | Boiling point | 386.1±37.0 °C(Predicted) | | density | 1.41±0.1 g/cm3(Predicted) | | vapor pressure | 0Pa at 20-25℃ | | storage temp. | room temp | | form | Powder | | color | White to Light yellow to Green | | Water Solubility | Soluble in methanol. Insoluble in water. | | BRN | 2263686 | | Major Application | diagnostic assay manufacturing
hematology
histology | | InChI | InChI=1S/C8H3N3O2/c9-4-6-2-1-3-8(11(12)13)7(6)5-10/h1-3H | | InChIKey | UZJZIZFCQFZDHP-UHFFFAOYSA-N | | SMILES | C1(C#N)=CC=CC([N+]([O-])=O)=C1C#N | | LogP | 0.3 at 25℃ | | Surface tension | 70.3mN/m at 212.5mg/L and 25℃ | | CAS DataBase Reference | 51762-67-5(CAS DataBase Reference) | | EPA Substance Registry System | 1,2-Benzenedicarbonitrile, 3-nitro- (51762-67-5) |
| Hazard Codes | Xn | | Risk Statements | 22-36/37/38-20/21/22 | | Safety Statements | 26-36-45-37/39 | | WGK Germany | 3 | | RTECS | CZ1953200 | | HS Code | 29269090 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Acute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| | 3-Nitrophthalonitrile Usage And Synthesis |
| Chemical Properties | light yellow powder | | Uses | 3-Nitrophthalonitrile can be used in solar cells. Dyes and metabolites. | | Application | 3-Nitrophthalonitrile belongs to nitrile derivatives and can be used as pesticide and pharmaceutical intermediates. It is an important intermediate for the synthesis of nitrophthalocyanine, nitrometallophthalocyanine or other phthalocyanine derivatives. | | Preparation | The synthesis of 3-nitrophthalonitrile started with the nitration in position 3 of phthalimide followed by the formation of 3-nitrophthalamide; then dehydration by the thionyl chloride in N, N-dimethylformamide leads to 3-nitrophthalonitrile.
Synthesis of 3-Nitrophthalonitrile | | Synthesis Reference(s) | Journal of Heterocyclic Chemistry, 32, p. 495, 1995 DOI: 10.1002/jhet.5570320219 |
| | 3-Nitrophthalonitrile Preparation Products And Raw materials |
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