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4-tert-Butylbenzyl chloride, 99%, Thermo Scientific Chemicals
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Catalog number A11856.06
also known as A11856-06
Price (USD)/ Each
64.00
-
Quantity:
5 g
Price (USD)/ Each
64.00
4-tert-Butylbenzyl chloride, 99%, Thermo Scientific Chemicals
Catalog numberA11856.06
Price (USD)/ Each
64.00
-
Chemical Identifiers
CAS19692-45-6
IUPAC Name1-tert-butyl-4-(chloromethyl)benzene
Molecular FormulaC11H15Cl
InChI KeyWAXIFMGAKWIFDQ-UHFFFAOYSA-N
SMILESCC(C)(C)C1=CC=C(CCl)C=C1
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Specifications
Specification Sheet
Specification SheetAppearance (Color)Clear colorless
FormLiquid
Assay (GC)≥98.5%
Refractive Index1.5190-1.5220 @ 20?C
4-tert-Butylbenzyl chloride has been used to control molecular weight and prevent microgel formation during polymerization reaction.
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
4-tert-Butylbenzyl chloride has been used to control molecular weight and prevent microgel formation during polymerization reaction.
Solubility
Slightly soluble in water.
Notes
Store in cool, dry conditions in well sealed container. Store away from oxidizing agent. Store away from strong bases.
4-tert-Butylbenzyl chloride has been used to control molecular weight and prevent microgel formation during polymerization reaction.
Solubility
Slightly soluble in water.
Notes
Store in cool, dry conditions in well sealed container. Store away from oxidizing agent. Store away from strong bases.
RUO – Research Use Only
General References:
- Sanford EM, et al. A comparison of 1, 4-bis (halomethyl) benzenes as monomers for the modified Gilch route to poly [2-methoxy-5-(2'-ethylhexyloxy)-p-phenylenevinylene]. CRC Handbook of Thermoelectronics.,1999, 23(1), 2347-48.
- Bing R. Hsieh; Yuan Yu; Eric W. Forsythe; Gregory M. Schaaf; and William A. Feld.A New Family of Highly Emissive Soluble Poly(p-phenylene vinylene) Derivatives. A Step toward Fully Conjugated Blue-Emitting Poly(p-phenylene vinylenes). J. Am. Chem. Soc.,1998, 120(1), 231-232 .