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Merck
CN

166170

Cinnamyl acetate

99%

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About This Item

Linear Formula:
CH3CO2CH2CH=CHC6H5
CAS Number:
103-54-8
Molecular Weight:
176.21
NACRES:
NA.22
PubChem Substance ID:
24850157
UNSPSC Code:
12352100
EC Number:
203-121-9
MDL number:
MFCD00008722

Key Documents

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Product Name

Cinnamyl acetate, 99%

InChI key

WJSDHUCWMSHDCR-VMPITWQZSA-N

InChI

1S/C11H12O2/c1-10(12)13-9-5-8-11-6-3-2-4-7-11/h2-8H,9H2,1H3/b8-5+

SMILES string

CC(=O)OC\C=C\c1ccccc1

assay

99%

form

powder

refractive index

n20/D 1.541 (lit.)

bp

265 °C (lit.)

solubility

alcohol: soluble(lit.)
glycerol: insoluble(lit.)
water: insoluble(lit.)

density

1.057 g/mL at 25 °C

Quality Level

100

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General description

Cinnamyl acetate is a fragrance ingredient. Palladium catalyzed allylic alkylation of cinnamyl acetate using sodium diethyl 2-methylmalonate and novel ferrocenyl Schiff base has been investigated.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H319

Hazard Classifications

Eye Irrit. 2

Storage Class

10 - Combustible liquids

wgk

WGK 1

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
SHBS9349
SHBS7929
SHBS6797
SHBR6065
SHBQ4212

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S P Bhatia et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 45 Suppl 1, S53-S57 (2007-11-23)
A toxicologic and dermatologic review of cinnamyl acetate when used as a fragrance ingredient is presented.
Schiff bases containing ferrocenyl and thienyl units and their utility in the palladium catalyzed allylic alkylation of cinnamyl acetate.
Pou D, et al
Journal of Organometallic Chemistry, 692(22), 5017-5025 (2007)
Ji-Eun Lee et al.
Pesticide biochemistry and physiology, 168, 104644-104644 (2020-07-28)
To find new and safe type of control agents against phytopathogenic fungi, the fumigant antifungal activity of 10 plant essential oils and constituents identified in cinnamon bark (Cinnamomum verum) and lemongrass (Cymbopogon citratus) essential oils was investigated against two phytopathogenic
Emilie Deletre et al.
Parasites & vectors, 8, 316-316 (2015-06-13)
Laboratory and field studies showed that repellent, irritant and toxic actions of common public health insecticides reduce human-vector contact and thereby interrupt disease transmission. One of the more effective strategies to reduce disease risk involves the use of long-lasting treated

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