6852-58-0

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6852-58-0 Structure

Identification	Back Directory
[Name] 2-METHYL-N-(PHENYLMETHYLENE)-2-PROPYLAMINE
[CAS] 6852-58-0
[Synonyms] TIMTEC-BB SBB008132 N-TERT-BUTYLBENZIMINE N-Benzylidene-N-tert-b N-tert-Butylbenzylimine N-tert-Butylbenzalimine N-BENZYLIDENE-T-BUTYLAMINE Benzylidene-tert-butylamine N-tert-Butylbenzylimine 97% N-tert-Butylbenzylideneamine N-BENZYLIDENE-TERT-BUTYLAMINE N-Benzylidene-N-tert-butylamine N-tert-butyl-1-phenylmethanimine N-tert-butyl-1-phenyl-methanimine N-Benzylidene-tert-butylamine 98% 2-Methyl-N-benzylidene-2-propanamine N-Benzylidene-1,1-dimethylethylamine N-Benzylidene-1,1-dimethylethanamine N-Benzylidene-2-methyl-2-propanamine N-Benzylidene-2-methylpropane-2-amine N-(tert-Butyl)-1-phenylmethanimine97% N-(tert-Butyl)-1-phenylmethanimine 97% Ethylamine, N-benzylidene-1,1-dimethyl- 2-methyl-n-(phenylmethylene)-2-propanamin 2-METHYL-N-(PHENYLMETHYLENE)-2-PROPANAMINE 2-METHYL-N-(PHENYLMETHYLENE)-2-PROPYLAMINE 2-Propanamine, 2-methyl-N-(phenylmethylene)- 2-Methyl-N-(phenylmethylene)-2-propylamine ,98% 2-Methyl-N-[(E)-phenylmethylidene]-2-propanamine 2-METHYL-N-(PHENYLMETHYLENE)-2-PROPYLAMINE ISO 9001：2015 REACH N-(tert-Butyl)benzylimine, N-Benzylidene-tert-butylamine, 2-Methyl-N-(phenylmethylene)propan-2-amine
[Molecular Formula] C11H15N
[MDL Number] MFCD00043553
[MOL File] 6852-58-0.mol
[Molecular Weight] 161.24

Chemical Properties	Back Directory
[Melting point ] -30
[Boiling point ] 209 °C(lit.)
[density ] 0.906 g/mL at 25 °C(lit.)
[refractive index ] n20/D 1.52(lit.)
[Fp ] 173 °F
[form ] liquid
[pka] 6.31±0.50(Predicted)
[color ] Colourless to light yellow
[Specific Gravity] 0.906
[EPA Substance Registry System] 2-Propanamine, 2-methyl-N-(phenylmethylene)- (6852-58-0)

Raw materials And Preparation Products	Back Directory
[Preparation Products] N-TERT-BUTYLBENZAMIDE-->2-BORONOBENZALDEHYDE, PINACOL ESTER-->N-(tert-Butyl)benzylamine-->N-tert-ButylbenzylaMine Hydrochloride

Hazard Information	Back Directory
[Chemical Properties] Colorless to yellow liquid
[Synthesis Reference(s)] The Journal of Organic Chemistry, 53, p. 5856, 1988 DOI: 10.1021/jo00260a012
[General Description] In vitro metabolism of N-benzyl-tert-butylamine in male hamster hepatic microsomal preparations has been studied. Kinetic studies of frustrated Lewis pair (FLP)-catalyzed hydrogenation and deuteration of N-benzylidene-tert-butylamine suggests that the reaction proceeds via autoinductive catalysis.

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