158844
2-Methylthio-2-imidazoline hydriodide
99%
Synonym(s):
2-Methylsulfanyl-4,5-dihydro-1H-imidazole hydrogen iodide
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25 G
₹11,496.15
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25 G
₹11,496.15
About This Item
Empirical Formula (Hill Notation):
C4H8N2S · HI
CAS Number:
Molecular Weight:
244.10
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
99%
form
powder
mp
144-146 °C (lit.)
functional group
thioether
SMILES string
I[H].CSC1=NCCN1
InChI
1S/C4H8N2S.HI/c1-7-4-5-2-3-6-4;/h2-3H2,1H3,(H,5,6);1H
InChI key
PZZRSEUDGCFXIH-UHFFFAOYSA-N
Application
2-Methylthio-2-imidazoline hydriodide was used in the preparation of starting materials required for the synthesis of 2-amino1-(2-Imidazolin-2-yl)-2-imidazoline.[1]
Reactant for synthesis of:
Aurora and epidermal growth factor receptor kinase inhibitors
Spiro-piperidine inhibitors against influenza A virus
Galegine analogues for aided weight loss in mice
Guanidinyl pyrrolidines as bifunctional catalysts for enantioselective conjugate additions to cyclic enones
Carbonic anhydrase inhibitors
Small molecule CXCR4 antagonists
Aurora and epidermal growth factor receptor kinase inhibitors
Spiro-piperidine inhibitors against influenza A virus
Galegine analogues for aided weight loss in mice
Guanidinyl pyrrolidines as bifunctional catalysts for enantioselective conjugate additions to cyclic enones
Carbonic anhydrase inhibitors
Small molecule CXCR4 antagonists
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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1-(2-Imidazolin-2-yl)-2-imidazolines. I. Structure of Jaffe's base and the chemistry of related compounds.
Wittekind RR, et al.
The Journal of Organic Chemistry, 38(9), 1641-1645 (1973)
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