200,000+ products from a single source!
sales@angenechem.com
Home > Imidazoles > 534-26-9
534-26-9 | 2-Methyl-4,5-dihydro-1H-imidazole
CAS No: 534-26-9 Catalog No: AG003HLW MDL No:MFCD00051490
Product Description
Catalog Number:
AG003HLW
Chemical Name:
2-Methyl-4,5-dihydro-1H-imidazole
CAS Number:
534-26-9
Molecular Formula:
C4H8N2
Molecular Weight:
84.1197
MDL Number:
MFCD00051490
IUPAC Name:
2-methyl-4,5-dihydro-1H-imidazole
InChI:
InChI=1S/C4H8N2/c1-4-5-2-3-6-4/h2-3H2,1H3,(H,5,6)
InChI Key:
VWSLLSXLURJCDF-UHFFFAOYSA-N
SMILES:
CC1=NCCN1
EC Number:
208-596-6
UNII:
987F50E3PE
Properties
Complexity:
75.6
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
84.069g/mol
Formal Charge:
0
Heavy Atom Count:
6
Hydrogen Bond Acceptor Count:
1
Hydrogen Bond Donor Count:
1
Isotope Atom Count:
0
Molecular Weight:
84.122g/mol
Monoisotopic Mass:
84.069g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
24.4A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.5
Literature
| Title | Journal |
|---|---|
| Efficient preparation of 2,4-diaminopyrimidine nucleosides: total synthesis of lysidine and agmatidine. | Organic letters 20120817 |
| Life without the essential bacterial tRNA Ile2-lysidine synthetase TilS: a case of tRNA gene recruitment in Bacillus subtilis. | Molecular microbiology 20110501 |
| Discovery and characterization of tRNAIle lysidine synthetase (TilS). | FEBS letters 20100121 |
| Structural basis for translational fidelity ensured by transfer RNA lysidine synthetase. | Nature 20091022 |
| Conformational preferences of hypermodified nucleoside lysidine (k2C) occurring at 'wobble' position in anticodon loop of tRNA(Ile). | Nucleosides, nucleotides & nucleic acids 20081001 |
| Tandem reactions of 1,3-diacid chlorides with 2-methylimidazoline and 2-methyl-1,4,5,6-tetrahydropyrimidine: one-pot synthesis of 1,8-naphthyridinetetraones. | The Journal of organic chemistry 20080704 |
| The many applications of acid urea polyacrylamide gel electrophoresis to studies of tRNAs and aminoacyl-tRNA synthetases. | Methods (San Diego, Calif.) 20080201 |
| Synthesis of heterocyclic compounds via nucleophilic aroylation catalyzed by imidazolidenyl carbene. | Chemical & pharmaceutical bulletin 20061201 |
| Unexpected ring expansion of an enantiopure imidazoline carbene ligand. | Organic letters 20060706 |
| molecular mechanism of lysidine synthesis that determines tRNA identity and codon recognition. | Molecular cell 20050722 |
| Enzymatic conversion of cytidine to lysidine in anticodon of bacterial isoleucyl-tRNA--an alternative way of RNA editing. | Trends in biochemical sciences 20040401 |
| An RNA-modifying enzyme that governs both the codon and amino acid specificities of isoleucine tRNA. | Molecular cell 20030901 |
| Nucleophilic acylation of arylfluorides catalyzed by imidazolidenyl carbene. | Chemical communications (Cambridge, England) 20030607 |
Related Products
Featured Products
© 2019 Angene International Limited. All rights Reserved.