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614-30-2

614-30-2 Structure

614-30-2 Structure
IdentificationMore
[Name]

N-METHYL-N-BENZYLANILINE
[CAS]

614-30-2
[Synonyms]

METHYLBENZYLANILINE
N-BENZYL N-METHYL ANILINE
N-METHYL-N-BENZYLANILINE
N-METHYL-N-PHENYLBENZYLAMINE
n-methyl-n-phenyl-benzenemethanamin
N-methyl-N-phenyl-Benzenemethanamine
N-Methyl-N-benzylanilin
Benzylmethylphenylamine
N-Phenyl-N-methylbenzylamine
[EINECS(EC#)]

210-375-4
[Molecular Formula]

C14H15N
[MDL Number]

MFCD00035788
[Molecular Weight]

197.28
[MOL File]

614-30-2.mol
Chemical PropertiesBack Directory
[Melting point ]

9.3°C
[Boiling point ]

318 °C(lit.)
[density ]

1.04 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.605(lit.)
[Fp ]

110 °C
[storage temp. ]

Store below +30°C.
[solubility ]

0.009g/l
[form ]

liquid
[pka]

4.38±0.50(Predicted)
[Water Solubility ]

0.009g/L
[FreezingPoint ]

8℃
[InChI]

InChI=1S/C14H15N/c1-15(14-10-6-3-7-11-14)12-13-8-4-2-5-9-13/h2-11H,12H2,1H3
[InChIKey]

LXZGVFCKZRHKMU-UHFFFAOYSA-N
[SMILES]

C1(CN(C)C2=CC=CC=C2)=CC=CC=C1
[CAS DataBase Reference]

614-30-2(CAS DataBase Reference)
[EPA Substance Registry System]

Benzenemethanamine, N-methyl-N-phenyl- (614-30-2)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
[WGK Germany ]

2
[Autoignition Temperature]

450 °C DIN 51794
[TSCA ]

TSCA listed
[HS Code ]

2921 49 00
[Toxicity]

LD50 orally in Rabbit: 2130 mg/kg
Raw materials And Preparation ProductsBack Directory
[Raw materials]

N-Methylaniline
[Preparation Products]

BASIC RED 46-->N-Benzylideneamine-->BASIC RED 46-->hydrogen [4-[[4-(dimethylamino)-3-sulphonatophenyl][4-[methyl(3-sulphonatobenzyl)amino]phenyl]methylene]cyclohexa-2,5-dien-1-ylidene]dimethylammonium, sodium salt
Hazard InformationBack Directory
[Uses]

N-Benzyl-N-methylaniline is a tertiary amine and a useful building block, used in the synthetic preparation of fused tetrahydroquinolines via oxidative cyclization of anilines with maleimides.
[Synthesis Reference(s)]

The Journal of Organic Chemistry, 60, p. 2677, 1995 DOI: 10.1021/jo00114a014
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