527750
4-(Hydroxymethyl)benzonitrile
95%
Synonym(s):
4-Cyanobenzyl alcohol
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About This Item
Linear Formula:
HOCH2C6H4CN
CAS Number:
Molecular Weight:
133.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2206193
Assay:
95%
InChI
1S/C8H7NO/c9-5-7-1-3-8(6-10)4-2-7/h1-4,10H,6H2
SMILES string
OCc1ccc(cc1)C#N
InChI key
XAASLEJRGFPHEV-UHFFFAOYSA-N
assay
95%
Quality Level
functional group
hydroxyl, nitrile
Related Categories
General description
4-(Hydroxymethyl)benzonitrile can be synthesized via hydrosilylation reaction in the presence of Fe complex Bu4N[Fe(CO)3(NO)] [catalyst]. It can also be prepared from 4-(aminomethyl) benzyl alcohol.
Application
4-(Hydroxymethyl)benzonitrile [p-(hydroxymethyl)benzonitrile] may be used to synthesize p-((vinyloxy)methyl)benzonitrile (VOMBN).
signalword
Warning
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Bu4N [Fe (CO)3(NO)]-Catalyzed Hydrosilylation of Aldehydes and Ketones.
Dieskau AP, et al.
European Journal of Organic Chemistry, 27, 5291-5296 (2011)
Bergstra?er U, et al.
Science of Synthesis: Houben-Weyl Methods of Molecular Transformations, 219-219 (2014)
Vinyl monomers bearing chromophore moieties and their polymers. VIII. synthesis and fluorescence behavior of a vinyloxy monomer having an electron-accepting chromophore moiety, p-((vinyloxy) methyl) benzonitrile, and its polymers.
Du FS, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 37(2), 179-187 (1999)
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