Home Imidazoles 534-26-9
534-26-9,MFCD00051490
Catalog No.:AA003HJ4
534-26-9 | 2-Methyl-4,5-dihydro-1H-imidazole
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1g
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5g
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$157.00
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25g
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  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA003HJ4
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
Computed 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  

Synonyms
 
4-amino-2-(N(6)-lysino)-1-ribofuranosylpyrimidine 
lysidine 
4,5-Dihydro-2-methyl-1H-imidazole 
UNII-987F50E3PE 
2-methyl imidazoline 
EINECS 208-596-6 
BRN 0104225 
AI3-16866 
2-methyl-4,5-dihydroimidazole 
2-Methyl-2-imidazoline, 95% 
VWSLLSXLURJCDF-UHFFFAOYSA-N 
987F50E3PE 
2-METHYL-2-IMIDAZOLINE 
MFCD00051490 
F1918-0077 
2-Methyl-20imidazolin 
Lysidin 
Methyl glyoxaidine 
4,5-Dihydro-2-methyl-1H-imidazol 
PubChem10179 
AC1L1VYT 
AC1Q2PFY 
4,5-Dihydro-2-methyl-1H-imidazol [IUPAC] 
534-26-9 
2-methyl4,5-dihydroimidazole 
5-23-03-00385 (Beilstein Handbook Reference) 
ACMC-209l79 
2-Methyl-.delta.2-imidazoline 
CHEMBL3935635 
DTXSID2060204 
CTK8B1840 
VWSLLSXLURJCDF-UHFFFAOYSA- 
KS-000010MX 
ZINC2034884 
Lysidine 
2-methyl-4,5-dihydro-1h imidazole 
ANW-31747 
SBB040067 
AKOS000271199 
MCULE-4787238872 
2-Methyl-4,5-dihydro-1H-imidazole # 
AK324582 
AN-45668 
LS-78467 
TC-120492 
2-Methyl-4,5-dihydro-1H-imidazole 
FT-0612921 
M0579 
ST50177681 
I14-49105 
InChI=1/C4H8N2/c1-4-5-2-3-6-4/h2-3H2,1H3,(H,5,6) 
4-methyl-2-imidazoline 
methyl-4,5-dihydro-1h-imidazole 
C4-H8-N2 
CID10798 
53517-93-4 
2-Methylimidazoline 
1H-Imidazole, 4,5-dihydro-2-methyl- 
Methylglyoxalidine 
2-Imidazoline, 2-methyl- 
Literature

Title: Efficient preparation of 2,4-diaminopyrimidine nucleosides: total synthesis of lysidine and agmatidine.

Journal: Organic letters 20120817

Title: Life without the essential bacterial tRNA Ile2-lysidine synthetase TilS: a case of tRNA gene recruitment in Bacillus subtilis.

Journal: Molecular microbiology 20110501

Title: Discovery and characterization of tRNAIle lysidine synthetase (TilS).

Journal: FEBS letters 20100121

Title: Structural basis for translational fidelity ensured by transfer RNA lysidine synthetase.

Journal: Nature 20091022

Title: Conformational preferences of hypermodified nucleoside lysidine (k2C) occurring at 'wobble' position in anticodon loop of tRNA(Ile).

Journal: Nucleosides, nucleotides & nucleic acids 20081001

Title: 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.

Journal: The Journal of organic chemistry 20080704

Title: The many applications of acid urea polyacrylamide gel electrophoresis to studies of tRNAs and aminoacyl-tRNA synthetases.

Journal: Methods (San Diego, Calif.) 20080201

Title: Synthesis of heterocyclic compounds via nucleophilic aroylation catalyzed by imidazolidenyl carbene.

Journal: Chemical & pharmaceutical bulletin 20061201

Title: Unexpected ring expansion of an enantiopure imidazoline carbene ligand.

Journal: Organic letters 20060706

Title: molecular mechanism of lysidine synthesis that determines tRNA identity and codon recognition.

Journal: Molecular cell 20050722

Title: Enzymatic conversion of cytidine to lysidine in anticodon of bacterial isoleucyl-tRNA--an alternative way of RNA editing.

Journal: Trends in biochemical sciences 20040401

Title: An RNA-modifying enzyme that governs both the codon and amino acid specificities of isoleucine tRNA.

Journal: Molecular cell 20030901

Title: Nucleophilic acylation of arylfluorides catalyzed by imidazolidenyl carbene.

Journal: Chemical communications (Cambridge, England) 20030607

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