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Thermo Scientific Chemicals
3-Methylbenzyl chloride, 98%
CAS: 620-19-9 | C8H9Cl | 140.61 g/mol
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Catalog number A10784.22
also known as A10784-22
Price (USD)
99.65
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Quantity:
100 g
Price (USD)
99.65
Online Exclusive
110.00Save 10.35 (9%)
Each
Chemical Identifiers
CAS620-19-9
IUPAC Name1-(chloromethyl)-3-methylbenzene
Molecular FormulaC8H9Cl
InChI KeyLZBOHNCMCCSTJX-UHFFFAOYSA-N
SMILESCC1=CC=CC(CCl)=C1
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Specifications
Specification Sheet
Specification SheetFormLiquid
Assay (GC)≥97.5%
Appearance (Color)Clear colorless to pale yellow
Refractive Index1.5330-1.5370 @ 20?C
3-Methylbenzyl chloride is used as an organic light-emitting diode and as an intermediate in organic synthesis.
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
3-Methylbenzyl chloride is used as an organic light-emitting diode and as an intermediate in organic synthesis.
Solubility
Not miscible or difficult to mix in water.
Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with bases and oxidizing agents.
3-Methylbenzyl chloride is used as an organic light-emitting diode and as an intermediate in organic synthesis.
Solubility
Not miscible or difficult to mix in water.
Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with bases and oxidizing agents.
RUO – Research Use Only
General References:
- Lionel Delaude.; Pierre Laszlo. Versatility of zeolites as catalysts for ring or side-chain aromatic chlorinations by sulfuryl chloride. J. Org. Chem. 1990, 55, (18), 5260-5269.
- Li-Jiau Huang.; Mei-Ling Shih.; Hua-Sin Chen.; Shiow-Lin Pan.; Che-Ming Teng.; Fang-Yu Lee.;Sheng-Chu Kuo. Synthesis of N2-(substituted benzyl)-3-(4-methylphenyl)indazoles as novel anti-angiogenic agents. Bioorganic & Medicinal Chemistry. 2006, 14 (2), 528-536.