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Assay
≥97.5% (GC)
98%
form
powder
optical activity
[α]/D 4.5±1.0°, c = 1 in chloroform
SMILES string
O=C1C[C@H]2C[C@@H]1CC2=O
InChI
1S/C7H8O2/c8-6-2-4-1-5(6)3-7(4)9/h4-5H,1-3H2/t4-,5-/m1/s1
InChI key
RVFBNLMXCXFOET-RFZPGFLSSA-N
Packaging
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Articles
Chiral diene ligands enable asymmetric transformations, constructing enantioenriched compounds from achiral substrates efficiently.
Chiral diene ligands enable asymmetric transformations, constructing enantioenriched compounds from achiral substrates efficiently.
Chiral diene ligands enable asymmetric transformations, constructing enantioenriched compounds from achiral substrates efficiently.
Chiral diene ligands enable asymmetric transformations, constructing enantioenriched compounds from achiral substrates efficiently.
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