Cinnamonitrile

Cinnamonitrile
Names
	IUPAC name (E)-3-phenylprop-2-enenitrile
	Other names trans-Cinnamonitrile; trans-β-Phenylacrylonitrile; (E)-3-Phenyl-2-propenenitrile; ;
Identifiers
CAS Number	1885-38-7; 4360-47-8 (unspecified geometry);
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL2387747;
ChemSpider	1267328;
ECHA InfoCard	100.015.957
EC Number	217-552-5;
PubChem CID	1550846;
UNII	H475UV3WWH;
CompTox Dashboard (EPA)	DTXSID8044385 ;
	InChI InChI=1S/C9H7N/c10-8-4-7-9-5-2-1-3-6-9/h1-7H/b7-4+ Key: ZWKNLRXFUTWSOY-QPJJXVBHSA-N;
	SMILES C(=C/C#N)\C1=CC=CC=C1;
Properties
Chemical formula	C9H7N
Molar mass	129.162 g·mol−1
Density	1.0374 (15.2 °C)
Melting point	22 °C (72 °F; 295 K)
Boiling point	263.8 °C (506.8 °F; 537.0 K)
log P	1.96
Hazards
	GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H301, H312, H317
Precautionary statements	P261, P264, P270, P272, P280, P301+P316, P302+P352, P317, P321, P330, P333+P313, P362+P364, P405, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

(E)-Cinnamonitrile is an organic compound approved for use as a fragrance in products such as air fresheners.^[2]^[3] It has a spicy cinnamon aroma.

References

^ "Cinnamonitrile". pubchem.ncbi.nlm.nih.gov.
^ "IFRA Standard, Amendment 49: Cinnamyl nitrile" (PDF). International Fragrance Association. 2020. Retrieved 2022-06-23.
^ "Cinnamonitrile". Consumer Product Information Database. Retrieved 2022-06-23.
^ Yu, Chao-sheng; Pan, Cheng-jun; Xie, Jin; Li, Bin (2007). "Quick synthesis of trans-cinnamyl nitrile". CNKI.
^ An, Xiao-De; Yu, Shouyun (2015). "Direct Synthesis of Nitriles from Aldehydes Using an O-Benzoyl Hydroxylamine (BHA) as the Nitrogen Source". Organic Letters. 17 (20): 5064–5067. doi:10.1021/acs.orglett.5b02547. PMID 26418564.
^ Obora, Yasushi; Okabe, Yoshihisa; Ishii, Yasutaka (2010). "journal Direct oxidative coupling of benzenes with acrylonitriles to cinnamonitriles catalyzed by Pd(OAc)₂/HPMoV/O₂ system". Organic & Biomolecular Chemistry. 8 (18): 4071–4073. doi:10.1039/c0ob00176g. PMID 20652185.

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