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| SKU | Size | Availability |
Price | Qty |
|---|---|---|---|---|
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T102746-5g
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5g |
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
|
$9.90
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T102746-10g
|
10g |
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
|
$13.90
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|
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T102746-25g
|
25g |
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
|
$25.90
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T102746-100g
|
100g |
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
|
$92.90
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T102746-500g
|
500g |
1
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$239.90
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| Synonyms | EN300-15137 | Pyrimidine, 2,4,6-trichloro- | F0001-1082 | NSC 6494 | Tox21_202916 | AM20100003 | EINECS 223-183-0 | NCGC00260462-01 | 2.4.6-Trichloropyrimidin | AC-2473 | CAS-3764-01-0 | AI3-26566 | 2,6-Trichloropyrimidine | FT-0609856 | PS-5328 | 2,4,6-T |
|---|---|
| Specifications & Purity | ≥98% |
| Shipped In | Normal |
| Product Description |
It is applied In selective Suzuki coupling with arylboronic acids has been reported to give 6-arylpyrimidines. |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Class | Diazines |
| Subclass | Pyrimidines and pyrimidine derivatives |
| Intermediate Tree Nodes | Halopyrimidines |
| Direct Parent | 2-halopyrimidines |
| Alternative Parents | Aryl chlorides Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organochlorides Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | 2-halopyrimidine - Aryl halide - Aryl chloride - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Organochloride - Organohalogen compound - Aromatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as 2-halopyrimidines. These are aromatic compounds containing a pyrimidine ring substituted at the 2-position with a halogen atom. |
| External Descriptors | Not available |
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| IUPAC Name | 2,4,6-trichloropyrimidine |
|---|---|
| INCHI | InChI=1S/C4HCl3N2/c5-2-1-3(6)9-4(7)8-2/h1H |
| InChIKey | DPVIABCMTHHTGB-UHFFFAOYSA-N |
| Smiles | C1=C(N=C(N=C1Cl)Cl)Cl |
| Isomeric SMILES | C1=C(N=C(N=C1Cl)Cl)Cl |
| WGK Germany | 3 |
| PubChem CID | 77378 |
| Molecular Weight | 183.42 |
| Beilstein | 118284 |
| Reaxy-Rn | 118284 |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Mar 21, 2024 | T102746 | |
| Certificate of Analysis | Sep 19, 2023 | T102746 | |
| Certificate of Analysis | Sep 19, 2023 | T102746 | |
| Certificate of Analysis | Sep 19, 2023 | T102746 | |
| Certificate of Analysis | Sep 19, 2023 | T102746 | |
| Certificate of Analysis | Jan 05, 2023 | T102746 | |
| Certificate of Analysis | Jan 05, 2023 | T102746 | |
| Certificate of Analysis | Jan 05, 2023 | T102746 | |
| Certificate of Analysis | Jan 05, 2023 | T102746 | |
| Certificate of Analysis | Jan 05, 2023 | T102746 |
| Solubility | Insoluble in water. |
|---|---|
| Freezing Point(°C) | 22 °C |
| Refractive Index | 1.57 |
| Flash Point(°F) | 235.4 °F |
| Flash Point(°C) | 112℃ |
| Boil Point(°C) | 210-215°C |
| Melt Point(°C) | 23-25°C |
| Molecular Weight | 183.420 g/mol |
| XLogP3 | 3.100 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | 181.921 Da |
| Monoisotopic Mass | 181.921 Da |
| Topological Polar Surface Area | 25.800 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 89.800 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Hanzhong Ren, Hao Liu, Rentong Qin, Hucheng Fu, Weixiang Xu, Rong Jia, Jia Jiang, Yizhang Yang, Yiting Xu, Birong Zeng, Conghui Yuan, Lizong Dai. (2025) Synergy strategy of multi-metals confined in heteroatom framework toward constructing high-performance water oxidation electrocatalysts. JOURNAL OF COLLOID AND INTERFACE SCIENCE, 680 (976). |