Cas no 25526-81-2 (4-Amino-5-bromomethyl-2-methylpyrimidine)
25526-81-2 structure
Product Name:4-Amino-5-bromomethyl-2-methylpyrimidine
CAS No:25526-81-2
MF:C6H8BrN3
MW:202.051819801331
CID:238459
PubChem ID:408390
Update Time:2025-04-19
4-Amino-5-bromomethyl-2-methylpyrimidine Chemical and Physical Properties
Names and Identifiers
-
- 4-Amino-5-bromomethyl-2-methylpyrimidine
- 4-Pyrimidinamine, 5-(bromomethyl)-2-methyl-
- 5-(bromomethyl)-2-methylpyrimidin-4-amine
- 2-Methyl-4-amino-5-brommethyl-pyrimidin
- 4-Amino-2-methyl-5-brommethylpyrimidin
- 4-Amino-5-brommethyl-2-methylpyrimidin
- 5-Brommethyl-2-methyl-pyrimidin-4-ylamin
- 5-bromomethyl-2-methyl-pyrimidin-4-ylamine
- 4-Pyrimidinamine, 5-(bromomethyl)-2-methyl- (9CI)
- DTXSID40328250
- 25526-81-2
- AKOS016006162
- SB59592
- 5-(bromomethyl)-2-methyl-pyrimidin-4-amine
- 4-Pyrimidinamine,5-(bromomethyl)-2-methyl-(9ci)
- Pyrimidine, 4-amino-5-(bromo-methyl)-2-methyl-
- SCHEMBL20310245
- FT-0712997
- EN300-44095
- CS-0089025
- PD126531
- AB06102
- 2-methyl-4-amino-5-bromomethylpyrimidine
-
- Inchi： 1S/C6H8BrN3/c1-4-9-3-5(2-7)6(8)10-4/h3H,2H2,1H3,(H2,8,9,10)
- InChI Key： QWNONVPLJDGJQR-UHFFFAOYSA-N
- SMILES： BrCC1=CN=C(C)N=C1N
Computed Properties
- Exact Mass: 200.99000
- Monoisotopic Mass: 200.99016g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 10
- Rotatable Bond Count: 1
- Complexity: 109
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 0.8
- Topological Polar Surface Area: 51.8?2
Experimental Properties
- PSA: 51.80000
- LogP: 1.84330
4-Amino-5-bromomethyl-2-methylpyrimidine Customs Data
- HS CODE：2933599090
- Customs Data：
China Customs Code:
2933599090Overview:
2933599090. Other compounds with pyrimidine ring in structure(Including other compounds with piperazine ring on the structure. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%
Declaration elements:
Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date
Summary:
2933599090. other compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
4-Amino-5-bromomethyl-2-methylpyrimidine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Chemenu | CM165168-1g |
5-(bromomethyl)-2-methylpyrimidin-4-amine |
25526-81-2 | 95% | 1g |
$430 | 2021-08-05 | |
| Alichem | A039002165-250mg |
4-Amino-5-(bromomethyl)-2-methylpyrimidine |
25526-81-2 | 98% | 250mg |
$340.65 | 2023-09-02 | |
| Alichem | A039002165-500mg |
4-Amino-5-(bromomethyl)-2-methylpyrimidine |
25526-81-2 | 98% | 500mg |
$557.80 | 2023-09-02 | |
| Alichem | A039002165-1g |
4-Amino-5-(bromomethyl)-2-methylpyrimidine |
25526-81-2 | 98% | 1g |
$1053.74 | 2023-09-02 | |
| Chemenu | CM165168-1g |
5-(bromomethyl)-2-methylpyrimidin-4-amine |
25526-81-2 | 95% | 1g |
$417 | 2024-07-28 | |
| Enamine | EN300-44095-0.05g |
5-(bromomethyl)-2-methylpyrimidin-4-amine |
25526-81-2 | 0.05g |
$639.0 | 2023-05-26 | ||
| Enamine | EN300-44095-0.1g |
5-(bromomethyl)-2-methylpyrimidin-4-amine |
25526-81-2 | 0.1g |
$670.0 | 2023-05-26 | ||
| Enamine | EN300-44095-0.25g |
5-(bromomethyl)-2-methylpyrimidin-4-amine |
25526-81-2 | 0.25g |
$700.0 | 2023-05-26 | ||
| Enamine | EN300-44095-0.5g |
5-(bromomethyl)-2-methylpyrimidin-4-amine |
25526-81-2 | 0.5g |
$731.0 | 2023-05-26 | ||
| Enamine | EN300-44095-1.0g |
5-(bromomethyl)-2-methylpyrimidin-4-amine |
25526-81-2 | 1g |
$761.0 | 2023-05-26 |
4-Amino-5-bromomethyl-2-methylpyrimidine Related Literature
-
1. 113. Aneurin. Part X. The mechanism of thiochrome formation from aneurin and aneurin disulphideP. Sykes,A. R. Todd J. Chem. Soc. 1951 534
-
A. R. Todd,F. Bergel J. Chem. Soc. 1937 364
-
3. 843. Isothiazoles. Part VII. Quaternary isothiazolesP. Chaplen,R. Slack,K. R. H. Wooldridge J. Chem. Soc. 1965 4577
-
4. 786. The synthesis of model intermediates related to thiamine-catalysed reactionsC. T. Eyles,P. Sykes,J. E. Downes J. Chem. Soc. 1965 4265
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