| Weight | 63.546 g/mol |
|---|---|
| Formula | Cu |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
COPPER
99148-46-6, 7440-50-8, 72480-60-5, 90294-97-6, 13982-06-4
Score:
#99 in Physics
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#243 in Biology
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#253 in Chemistry
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- COPPER ENZYMES IN ISOLATED CHLOROPLASTS. POLYPHENOLOXIDASE IN BETA VULGARIS (Plant Physiology, 1949)
- A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective Ligation of Azides and Terminal Alkynes (Angewandte Chemie, 2002)
- Large-Area Synthesis of High-Quality and Uniform Graphene Films on Copper Foils (Science, 2009)
- Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides (Journal of Organic Chemistry, 2002)
- Synthesis, structure, and spectroscopic properties of copper(II) compounds containing nitrogensulphur donor ligands; the crystal and molecular structure of aqua[1,7-bis(N-methylbenzimidazol-2-yl)-2,6-dithiaheptane]copper(II) perchlorate (Journal of The Chemical Society-dalton Transactions, 1984)
- Development of a DTPA soil test for zinc, iron, manganese and copper (Soil Science Society of America Journal, 1978)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H317: May cause an allergic skin reaction
Warning Sensitization, Skin - Category 1 -
SMILES[Cu]
-
InChIKeyRYGMFSIKBFXOCR-UHFFFAOYSA-N
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(7440-39-3)
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(1317-38-0)
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(14694-69-0)
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(7723-14-0)
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(7440-09-7, 24203-36-9)
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(13983-20-5)
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(1317-40-4, 19138-68-2)
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(7439-88-5, 1602-20-6, 22542-08-1)
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COPPER
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