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P16753

Sigma-Aldrich

Phenylacetyl chloride

98%

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Synonym(s):
α-Toluyl chloride
Linear Formula:
C6H5CH2COCl
CAS Number:
Molecular Weight:
154.59
Beilstein:
742254
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

refractive index

n20/D 1.5325 (lit.)

bp

94-95 °C/12 mmHg (lit.)

density

1.169 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

ClC(=O)Cc1ccccc1

InChI

1S/C8H7ClO/c9-8(10)6-7-4-2-1-3-5-7/h1-5H,6H2

InChI key

VMZCDNSFRSVYKQ-UHFFFAOYSA-N

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Application

Phenylacetyl chloride is used as a key precursor in the total synthesis of vialinin B. It is employed as a linker to prepare dendrimers and also used in the synthesis of various conjugated aromatic small molecules.

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

8A - Combustible, corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

215.6 °F

Flash Point(C)

102 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品

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Solution-processable α, ω-distyryl oligothiophene semiconductors with enhanced environmental stability.
Mauldin C E, et al.
Chemistry of Materials, 21(9), 1927-1938 (2009)
New electron-accepting π-conjugated polyquinoxalines with fluorene unit: synthesis and light-emitting properties.
Jung S H, et al.
Polym. Bull., 50(4), 251-258 (2003)
Polyaryl ether dendrimer with a 4-phenylacetyl-5-pyrazolone-based terbium (III) complex as core: synthesis and photopysical properties.
Shen L, et al.
Inorganic Chemistry, 45(16), 6188-6197 (2006)
A Light-Harvesting Array Composed of Porphyrins and Rigid Backbones.
Kozaki M, et al.
Organic Letters, 10(20), 4477-4480 (2008)
Expeditious synthesis of vialinin B, an extremely potent inhibitor of TNF-α production.
Ye Y Q, et al.
Organic Letters, 11(21), 5074-5077 (2009)

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