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Methyl tiglate, 98%, Thermo Scientific Chemicals
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Catalog number A11964.18
also known as A11964-18
Price (USD)/ Each
141.00
-
Quantity:
50 g
Price (USD)/ Each
141.00
Methyl tiglate, 98%, Thermo Scientific Chemicals
Catalog numberA11964.18
Price (USD)/ Each
141.00
-
Chemical Identifiers
CAS6622-76-0
IUPAC Namemethyl (2Z)-2-methylbut-2-enoate
Molecular FormulaC6H10O2
InChI KeyYYJWBYNQJLBIGS-PLNGDYQASA-N
SMILESCOC(=O)C(C)=C/C
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Specifications
Specification Sheet
Specification SheetAppearance (Color)Clear colorless
Assay (GC)≥97.5%
Refractive Index1.4350-1.4390 @ 20?C
FormLiquid
It is employed as a perfuming agent in cosmetics industry.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
It is employed as a perfuming agent in cosmetics industry.
Solubility
Soluble in alcohol, water 3813 mg/L @ 25°C (est).
Notes
Store away from oxidizing agents. Keep the container tightly closed. Store in cool, dry conditions in well ventilated place.
It is employed as a perfuming agent in cosmetics industry.
Solubility
Soluble in alcohol, water 3813 mg/L @ 25°C (est).
Notes
Store away from oxidizing agents. Keep the container tightly closed. Store in cool, dry conditions in well ventilated place.
RUO – Research Use Only
General References:
- Herbert O. House.; Gary H. Rasmusson. Stereoselective. Synthesis of α-Substituted α,β-Unsaturated Esters.J. Org. Chem.,1961,26(11), 4278-4281.
- Hirokazu Urabe.; Isao Kuwajima. A cyclopentanone annulation via intramolecular acylation of alkylsilanes.J. Org. Chem.,1984,49(6), 1140-1141.
- Lithiation and alkylation with allylic rearrangement with 1-iodo-3-trimethylsilylpropane has been used in a versatile cyclopentanone synthesis: J. Org. Chem., 49, 1140 (1984); Org. Synth. Coll., 8, 486 (1993):