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Merck
CN

P16753

Phenylacetyl chloride

98%

Synonym(s):

α-Toluyl chloride

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About This Item

Linear Formula:
C6H5CH2COCl
CAS Number:
Molecular Weight:
154.59
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-146-5
Beilstein/REAXYS Number:
742254
MDL number:
Assay:
98%
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InChI key

VMZCDNSFRSVYKQ-UHFFFAOYSA-N

InChI

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

SMILES string

ClC(=O)Cc1ccccc1

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

Quality Level

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.

flash_point_f

215.6 °F

pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_c

102 °C

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
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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
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)
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)
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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