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grade
puriss.
Quality Level
Assay
≥99.0% (GC)
form
solid
reaction suitability
reaction type: Coupling Reactions
bp
122-124 °C/6 mmHg (lit.)
mp
32.0-37.0 °C
34-35 °C (lit.)
solubility
methylene chloride: 0.1 g/mL, clear, colorless
application(s)
peptide synthesis
SMILES string
C1CCC(CC1)N=C=NC2CCCCC2
InChI
1S/C13H22N2/c1-3-7-12(8-4-1)14-11-15-13-9-5-2-6-10-13/h12-13H,1-10H2
InChI key
QOSSAOTZNIDXMA-UHFFFAOYSA-N
Gene Information
human ... EPHX2(2053)
mouse ... Ephx2(13850)
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General description
Application
It may be also used to synthesize:
- 1,3-Thiazetedine derivatives via [2+2] cycloaddition with 2-phenylethenyl- and 2-(4-nitrophenyl)ethenyl isothiocyanates.
- 1,3,5-Oxadiazine-4-thiones via [4+2] cycloaddition with benzoyl isothiocyanates.
- Sterically hindered 1,3,4-oxadiazole derivatives by reacting with (N-isocyanimino)triphenylphosphorane the presence of aromatic (or heteroaromatic) carboxylic acids.
Other Notes
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Sens. 1
WGK
WGK 3
Flash Point(F)
closed cup
Flash Point(C)
closed cup
Personal Protective Equipment
Certificates of Analysis (COA)
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