Basic information
- Standard SMILES
N#CC(c1ccccc1)c1ccccc1- InChIKey
NEBPTMCRLHKPOB-UHFFFAOYSA-N- Molecular formula
- C14H11N
- Average molar mass
- 193.24 g/mol
- Monoisotopic mass
- 193.08914936
Names & identifiers
- Preferred name
- Diphenylacetonitrile
- IUPAC
- 2,2-diphenylacetonitrile
- English name
- Diphenylacetonitrile
- Molecular formula
- C14H11N
- Molecular weight
- 193.25
Names & synonyms
Show more names
Database identifiers
- CAS
86-29-3- PubChem CID
- 6837
- DTXSID
DTXSID4020539- ChEMBL
CHEMBL3185477- UNII
- QK4W106TKU
- EC Number
- 201-662-5
- Nikkaji
- J4.937I
Properties
Computed structural properties
- XLogP
- 3.2
- Topological polar surface area
- 23.8 Ų
- Hydrogen bond donors
- 0
- Hydrogen bond acceptors
- 1
- Rotatable bonds
- 2
- Heavy atoms
- 15
- Formal charge
- 0
- Complexity
- 207
Physicochemical properties
- Melting point
- 71 · 71-73 °C (lit.)
- Boiling point
- 181 °C/12 · 181 °C/12 mmHg (lit.)
- Density
- 1.1061 · 1.1061 (rough estimate)
- vapor pressure
- 21.3 hPa · 21.3 hPa (190 °C)
- refractive index
- 1.585 · 1.5850 (estimate)
- Flash point
- 120 °C · 120 °C
- storage temp.
- 30 °C · Store below +30°C.
- solubility
- INSOLUBLE
- form
- Crystalline Powder
- color
- White to creamy or faint yellow
- Water Solubility
- INSOLUBLE
- Merck
- 14 · 14,3316
- BRN
- 1911160 · 1911160
- Exposure limits
- 25 mg/m3 · NIOSH: IDLH 25 mg/m3
- InChI
- 1S/C14H11N/c15-11-14(12-7-3-1-4-8-12)13-9-5-2-6-10-13/h1-10,14H
- InChIKey
- NEBPTMCRLHKPOB-UHFFFAOYSA-N
- SMILES
- N#CC(c1ccccc1)c2ccccc2
- LogP
- 2.795 · 2.795-3.197 at 25℃
- CAS DataBase Reference
- 86 · 86-29-3(CAS DataBase Reference)
- EWG's Food Scores
- 1 · 1
- FDA UNII
- 4 W106TKU · QK4W106TKU
- NIST Chemistry Reference
- Benzeneacetonitrile, «alpha»-phenyl-(86-29-3)
- EPA Substance Registry System
- Diphenylacetonitrile (86-29-3)
- UNSPSC Code
- 12352117 · 12352117
- NACRES
- 22 · NA.22
- Symbol(GHS)
- 7 · GHS07
- Signal word
- Warning
- Hazard statements
- 303 · H303-H335-H315-H319
- Precautionary statements
- 264 · P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P261-P280a-P304+P340-P305+P351+P338-P405-P501a
- PPE
- 95 · dust mask type N95 (US), Eyeshields, Gloves
- Hazard Codes
- Xi
- Risk Statements
- 36 · 36/37/38
- Safety Statements
- 26 · 26-36-37/39
- WGK Germany
- 2 · 2
- RTECS
- 9800000 · AL9800000
- TSCA
- TSCA listed
- HS Code
- 29269095 · 29269095
- Storage Class
- 11 · 11 - Combustible Solids
- Hazard Classifications
- 2 · Aquatic Chronic 2
- Toxicity
- 50 orally · LD50 orally in Rabbit: 3500 mg/kg
- REACH Registrations
- Active
Safety & regulation
Safety data
- PPE
- dust mask type N95 (US), Eyeshields, Gloves
- wgk
- 2
- tsca
- TSCA listed
- rtecs
- AL9800000
- hs_code
- 29269095
- Toxicity
- LD50 orally in Rabbit: 3500 mg/kg
- risk_code
- 36/37/38
- Signal word
- Warning
- Symbol(GHS)
- GHS07
- hazard_code
- Xi
- safety_code
- 26-36-37/39
- Storage Class
- 11 - Combustible Solids
- Hazard statements
- H303-H335-H315-H319
- REACH Registrations
- Active
- Hazard Classifications
- Aquatic Chronic 2
- Precautionary statements
- P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P261-P280a-P304+P340-P305+P351+P338-P405-P501a
Chemistry & industry
Applications
UsesMathadone (M225865) impurity. Used in synthesis of methadone, antispasmodics and other pharmaceuticals.Diphenylacetonitrile is used to synthesize isocyanate, which is further prepared into UV paint, PU paint, transparent elastomer and adhesive, etc. In addition, it is also used in polyamide and epoxy resin industries.
General DescriptionDiphenylacetonitrile can be prepared in good yield by the dehydration of the amide of diphenyl acetic acid with phosphorous oxychloride.
Preparation methods
PreparationDiphenylacetonitrile can be prepared in good yield by the dehydration of the amide of diphenyl acetic acid with phosphorous oxychloride. Diphenylacetonitrile undergoes anhydrous condensation with ethyl-4-bromo-butyrate. This is followed by its hydrolysis in alkaline medium that is used in the quantitative determination of 3-cyano-3,3-diphenylpropionic acid.
PreparationIn a 100 mL, nitrogen-flushed pear flask was added indium(III) bromide (2.0 mmol, 10 mol %) in CH2Cl2 (40 mL) to give a white suspension. To this at room temperature was added trimethylsilyl cyanide (40 mmol, 2.0 equiv.), followed by dropwise addition of alcohol (20 mmol, 1.0 equiv.) to give a moderate exothermic reaction. The mixture slowly turned clear, and TLC showed mostly the desire product. Saturated NaHCO3 was added and the mixture was concentrated in vacuo to remove the volatiles. The residue was partitioned between saturated NaHCO3 and ethyl acetate, and the aqueous layer was extracted one more time with ethyl acetate. Combined organic layers were dried over MgSO4, filtered and concentrated. The crude product was purified by flash column chromatography on silica gel (5% ethyl acetate/hexanes) to give the desired Diphenylacetonitrile.
Upstream & downstream products
Upstream raw materials
Downstream products
Suppliers50 total
Related reactions
Linked notes
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