- 1,2-Diaminocyclohexane
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- $50.00 / 1KG
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2024-08-23
- CAS:694-83-7
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 10000kg
- 1,2-Diaminocyclohexane
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- $100.00 / 1KG
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2023-12-26
- CAS:694-83-7
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: g-kg-tons, free sample is available
- 1,2-Diaminocyclohexane
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- $0.00 / 25KG
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2023-08-30
- CAS:694-83-7
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 50000KG/month
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| 1,2-Diaminocyclohexane Basic information |
Product Name: | 1,2-Diaminocyclohexane | Synonyms: | 1,2-DIAMINOCYCLOHEXANE;(1R,2R)-(-)-1,2-CYCLOHEXANEDIAMINE;(1R)-TRANS-1,2-CYCLOHEXANEDIAMINE;(1R)-(-)-TRANS-1,2-DIAMINOCYCLOHEXANE;(1R)-TRANS-1,2-DIAMINOCYCLOHEXANE;1,2-Cylohexanediamine;1,2-Diaminocyclohexane,c&t;1,2-diaMinocylohexane | CAS: | 694-83-7 | MF: | C6H14N2 | MW: | 114.19 | EINECS: | 211-776-7 | Product Categories: | | Mol File: | 694-83-7.mol | ![1,2-Diaminocyclohexane Structure](CAS/GIF/694-83-7.gif) |
| 1,2-Diaminocyclohexane Chemical Properties |
Melting point | 41-45 °C | Boiling point | 92-93 °C18 mm Hg(lit.) | density | 0.931 g/mL at 25 °C(lit.) | vapor pressure | 0.4 mm Hg ( 20 °C) | refractive index | n20/D 1.49(lit.) | Fp | 169 °F | storage temp. | 2-8°C | form | Liquid | pka | 10.76±0.70(Predicted) | color | Clear | PH | 11.3 (5g/l, H2O, 20℃)neutral | Water Solubility | miscible | Sensitive | Air Sensitive | BRN | 506142 | LogP | 0 at 20℃ | CAS DataBase Reference | 694-83-7(CAS DataBase Reference) | NIST Chemistry Reference | 1,2-Cyclohexanediamine(694-83-7) | EPA Substance Registry System | 1,2-Cyclohexanediamine (694-83-7) |
| 1,2-Diaminocyclohexane Usage And Synthesis |
Chemical Properties | clear slightly yellow to yellow liquid | Uses | 1,2-Diaminocyclohexane was used in the synthesis of chiral ruthenium(IV)-oxo complexes. | Uses | suzuki reaction | Uses | 1,2-Diaminocyclohexane was used in the synthesis of chiral ruthenium(IV)-oxo complexes & bicyclic pyrazine derivatives. | Definition | ChEBI: Cyclohexane-1,2-diamine is a primary aliphatic amine. | General Description | 1,2-Diaminocyclohexane undergoes non-templated reaction with homochiral as well as the racemic form of trans-1,2-diaminocyclohexane with terephthaldehyde to yield (3+3)-cyclocondensed molecular triangles. It acts as ligand and forms organotin complexes, having potential applications as metal-based antitumour drugs. | Flammability and Explosibility | Non flammable |
| 1,2-Diaminocyclohexane Preparation Products And Raw materials |
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