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P16753

Sigma-Aldrich

Phenylacetyl chloride

98%

Synonym(s):

α-Toluyl chloride

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About This Item

Linear Formula:
C6H5CH2COCl
CAS Number:
103-80-0
Molecular Weight:
154.59
Beilstein:
742254
EC Number:
203-146-5
MDL number:
MFCD00000729
UNSPSC Code:
12352100
PubChem Substance ID:
24898236
NACRES:
NA.22

Quality Level

200

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
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H290,H314,H335

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

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Certificates of Analysis (COA)

Lot/Batch Number
STBK5001
STBK2163
STBJ9037
STBJ6662
0000084724

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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)
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)
Xiao-Yan Zhang et al.
Journal of agricultural and food chemistry, 66(34), 8976-8982 (2018-08-11)
Five new resorcylic acid lactones (RALs) hispidulactones A-E (1, 4, 5, 8, and 9), a new natural product (2), and four known ones (3, 6, 7, and 10) with different ring systems were isolated from the desert plant endophytic fungus
Solution-processable α, ω-distyryl oligothiophene semiconductors with enhanced environmental stability.
Mauldin C E, et al.
Chemistry of Materials, 21(9), 1927-1938 (2009)
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