2-Phenylpropan-2-amine supplier

Name
CUMYLAMINE
EINECS
CAS No. 585-32-0
Article Data40
CAS DataBase
Density 0.944 g/cm³
Solubility Insoluble in water.
Melting Point 116°C (estimate)
Formula C₉H₁₃N
Boiling Point 196.499 °C at 760 mmHg
Molecular Weight 135.209
Flash Point 84.05 °C
Transport Information UN2735
Appearance Liquid. (Clear, colorless ~ yellow.)
Safety 26-36/37/39
Risk Codes 36/37/38
Molecular Structure
Hazard Symbols T
Synonyms Benzylamine,a,a-dimethyl- (8CI);(2-Phenyl-2-propyl)amine;1-Methyl-1-phenylethylamine;1-Phenylisopropylamine;2-Amino-2-phenylpropane;2-Phenyl-2-propanamine;Cumylamine;NSC 66156;a,a-Dimethylbenzenemethanamine;a,a-Dimethylbenzylamine;
PSA 26.02000
LogP 2.58070

Synthetic route

: 32366-26-0
cumyl azide

: 585-32-0
2-phenyl-2-propylamine

Conditions

Conditions	Yield
With lithium aluminium tetrahydride In diethyl ether at 0 - 20℃; for 18h;	95%
With hydrogen In ethanol for 12h;	94%
With lithium aluminium tetrahydride In diethyl ether 1.) 12 h, 2.) reflux, 1 h;	68%

: 917-54-4
methyllithium

: 100-47-0
benzonitrile

: 585-32-0
2-phenyl-2-propylamine

Conditions

Conditions	Yield
With cerium(III) chloride	90%

: 79649-68-6
N-(1-methyl-1phenylethyl)acetamide

: 585-32-0
2-phenyl-2-propylamine

Conditions

Conditions	Yield
With ammonium bromide; ethylenediamine at 100℃; for 10h; Microwave irradiation;	88%

: 94616-84-9
dichloromethylcerium

: 55-21-0
benzamide

A: 100-47-0
benzonitrile

B: 585-32-0
2-phenyl-2-propylamine

Conditions

Conditions	Yield
at -78 - 0℃; for 2h; 5.0 equival. MeCeCl2;	A n/a B 73%

...Expand

: 4747-74-4
α,α-dimethylbenzyl isocyanate

: 585-32-0
2-phenyl-2-propylamine

Conditions

Conditions	Yield
With hydrogenchloride In water 70-80 deg C, 0.5 h; reflux, 0.5 h;	72%

: 94616-84-9
dichloromethylcerium

: 2227-79-4
benzenecarbothioamide

A: 100-47-0
benzonitrile

B: 585-32-0
2-phenyl-2-propylamine

Conditions

Conditions	Yield
at -78 - 0℃; for 2h; 5.0 equival. MeCeCl2;	A n/a B 68%

...Expand

: 3575-19-7
2-bromo-2-phenylpropane

: 585-32-0
2-phenyl-2-propylamine

Conditions

Conditions	Yield
With ammonia	53%
With ammonia

: 676-58-4
methylmagnesium chloride

: 100-47-0
benzonitrile

: 585-32-0
2-phenyl-2-propylamine

Conditions

Conditions	Yield
With titanium(IV) isopropylate In diethyl ether for 10h; Heating;	44%

: 826-54-0
2-methyl-2-phenyl-propanamide

: 585-32-0
2-phenyl-2-propylamine

Conditions

Conditions	Yield
With bromine
With alkaline aqueous sodium hypobromite

: 617-94-7
1-methyl-1-phenylethyl alcohol

: 585-32-0
2-phenyl-2-propylamine

Conditions

Conditions	Yield
With potassium cyanide; sulfuric acid In dibutyl ether at 60 - 80℃;
Multi-step reaction with 2 steps 1: 95 percent / LiAlH4 / diethyl ether / 18 h / 0 - 20 °C View Scheme
Multi-step reaction with 2 steps 1: NaN3; TFA / CHCl3 / 12 h / 20 °C 2: 19.8 g / H2 / Lindlar's catalyst / ethanol / 12 h View Scheme

: 17797-08-9
p-(2-Aminoprop-2-yl)-isopropylbenzol

: 585-32-0
2-phenyl-2-propylamine

Conditions

Conditions	Yield
With hydrogenchloride; aluminium trichloride In toluene

: 42044-69-9
N-formyl-α,α-dimethylbenzylamine

: 585-32-0
2-phenyl-2-propylamine

Conditions

Conditions	Yield
With potassium hydroxide In ethylene glycol
(alkaline hydrolysis);
With sodium hydroxide In water

: 38206-14-3
N-Isopropylidene-benzenesulfenamide

: 591-51-5
phenyllithium

: 585-32-0
2-phenyl-2-propylamine

Conditions

Conditions	Yield
(i) Et2O, (ii) H2O; Multistep reaction;

: 3457-58-7
2-nitro-2-phenylpropane

A: 1889-67-4
dicumene

B: 585-32-0
2-phenyl-2-propylamine

Conditions

Conditions	Yield
With potassium hydroxide; nickel In ethanol at 20℃; pH=13; Reduction; Electrolysis;	A 2 % Chromat. B 97 % Chromat.

β-nitro-β-phenyl-propane: β-nitro-β-phenyl-propane

: 585-32-0
2-phenyl-2-propylamine

Conditions

Conditions	Yield
With ethanol; acetic acid; zinc
With hydrogenchloride; tin; ethanol

11-chloro-1-isopropyl-benzene: 11-chloro-1-isopropyl-benzene

: 585-32-0
2-phenyl-2-propylamine

Conditions

Conditions	Yield
With ammonia at 20℃;

: 826-54-0
2-methyl-2-phenyl-propanamide

: 7726-95-6
bromine

alkali: alkali

: 585-32-0
2-phenyl-2-propylamine

...Expand

: 3457-58-7
2-nitro-2-phenylpropane

: 64-19-7
acetic acid

zinc dust: zinc dust

A: 98-86-2
acetophenone

B: 585-32-0
2-phenyl-2-propylamine

...Expand

: 1611-48-9
(1-methyl-1-phenyl-ethyl)-carbamic acid ethyl ester

: 7664-41-7
ammonia

A: 58609-76-0
(1-methyl-1-phenyl-ethyl)-urea

B: 57-13-6
urea

C: 51-79-6
urethane

D: 585-32-0
2-phenyl-2-propylamine

Conditions

Conditions	Yield
at 180 - 185℃;

...Expand

: N'-[1-(1-Methyl-1-phenyl-ethylamino)-meth-(Z)-ylidene]-hydrazinecarboxylic acid methyl ester

: 67-56-1
methanol

A: 4-(1-methyl-1-phenyl-ethyl)-2,4-dihydro-[1,2,4]triazol-3-one

B: methyl (2E)-2-[1-(methyloxy)methylidene]hydrazinecarboxylate

C: 585-32-0
2-phenyl-2-propylamine

Conditions

Conditions	Yield
With sodium methylate at 75℃;

...Expand

: 100-58-3
phenylmagnesium bromide

: 585-32-0
2-phenyl-2-propylamine

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: diethyl ether / 1 h / Ambient temperature 2: sodium azide, trifluoracetic acid / CHCl3 / 15 h / 5 - 20 °C 3: lithiumaluminium hydride / diethyl ether / 3 h / Ambient temperature View Scheme

: 98-83-9
isopropenylbenzene

: 585-32-0
2-phenyl-2-propylamine

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: NaN3, Cl3CCOOH / CHCl3 / 2 h / Heating 2: 61.5 percent / LiAlH4 / diethyl ether / 4 h / Heating View Scheme
Multi-step reaction with 2 steps 2: aq. NaOH / H2O View Scheme

: 98-83-9
isopropenylbenzene

CBrCl3: CBrCl3

: 585-32-0
2-phenyl-2-propylamine

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: aq. H2SO4 2: (alkaline hydrolysis) View Scheme
Multi-step reaction with 2 steps 1: NaN3, CF3CO2H / CHCl3 2: Raney-Ni / propan-2-ol View Scheme

: 100-18-5
1,4-bis(1-methylethyl)benzene

: 585-32-0
2-phenyl-2-propylamine

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: NCl3, AlCl3, tBuBr / 1,2-dichloro-ethane 2: AlCl3, HCl / toluene View Scheme

: 75-16-1
methylmagnesium bromide

: 100-47-0
benzonitrile

: 585-32-0
2-phenyl-2-propylamine

Conditions

Conditions	Yield
Stage #1: methylmagnesium bromide; benzonitrile In tetrahydrofuran; diethyl ether at 100℃; for 0.166667h; Double Grignard addition; Microwave irradiation; Stage #2: With titanium(IV) isopropylate In tetrahydrofuran; diethyl ether at 50℃; for 1h; Double Grignard addition; Microwave irradiation;
Stage #1: methylmagnesium bromide; benzonitrile In diethyl ether at 20℃; for 0.5h; Inert atmosphere; Stage #2: With titanium(IV) isopropylate In diethyl ether for 10h; Inert atmosphere;

: 107955-92-0
N-hydroxy-2-methyl-2-phenylpropanamide

: 585-32-0
2-phenyl-2-propylamine

Conditions

Conditions	Yield
Stage #1: N-hydroxy-2-methyl-2-phenylpropanamide With acetic anhydride; potassium carbonate In dimethyl sulfoxide at 50℃; for 24h; Lossen Rearrangement; Stage #2: With hydrogenchloride In water; dimethyl sulfoxide at 0℃;

: 98-86-2
acetophenone

: 585-32-0
2-phenyl-2-propylamine

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1.1: magnesium / diethyl ether / 1 h / Inert atmosphere; Reflux 1.2: 0 - 5 °C 2.1: trifluoroacetic acid; sodium azide / dichloromethane / -5 - 0 °C / Inert atmosphere 3.1: lithium aluminium tetrahydride / tetrahydrofuran / 0 - 20 °C / Inert atmosphere View Scheme

: N-(1-methyl-1-phenylethyl)-N'-(tert-butoxycarbonyl)hydrazinecarboxylic acid tert-butyl ester

: 585-32-0
2-phenyl-2-propylamine

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: dichloromethane / 1 h / 20 °C 2: hydrogen / methanol / 12 h View Scheme

: C9H14N2*C2HF3O2

: 585-32-0
2-phenyl-2-propylamine

Conditions

Conditions	Yield
With hydrogen In methanol for 12h;

: 100-07-2
4-methoxy-benzoyl chloride

: 585-32-0
2-phenyl-2-propylamine

: 454479-63-1
4-methoxy-N-(1-methyl-1-phenylethyl)benzamide

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0℃; for 18h;	100%
With triethylamine In dichloromethane for 12h;	87%
In tetrahydrofuran at 0℃;	84%
With triethylamine In dichloromethane Acylation;

: 874-98-6
1-bromomethyl-3-methoxybenzene

: 585-32-0
2-phenyl-2-propylamine

: 454479-64-2
N-(3-methoxybenzyl)-N-(1-methyl-1-phenylethyl)amine

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide for 12h;	100%

: 701-27-9
3-fluorobenzene-1-sulfonyl chloride

: 585-32-0
2-phenyl-2-propylamine

: 1312206-53-3
N-(2-phenylpropan-2-yl)-3-fluorobenzenesulfonamide

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0 - 20℃; Inert atmosphere;	100%

: 2888-06-4
3-chlorophenylsulfonyl chloride

: 585-32-0
2-phenyl-2-propylamine

: 1312206-54-4
N-(2-phenylpropan-2-yl)-3-chloro-benzenesulfonamide

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0 - 20℃; Inert atmosphere;	100%

: 2950-83-6
4-(2,4-dioxo-1,2,3,4-tetrahydro-1-pyrimidinyl)butanoic acid

: 585-32-0
2-phenyl-2-propylamine

: 1370293-09-6
4-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-N-(2-phenylpropan-2-yl)butanamide

Conditions

Conditions	Yield
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 20℃; for 3h;	100%

: 64-18-6
formic acid

: 585-32-0
2-phenyl-2-propylamine

: 42044-69-9
N-formyl-α,α-dimethylbenzylamine

Conditions

Conditions	Yield
Stage #1: formic acid With acetic acid at 25℃; for 1h; Stage #2: 2-phenyl-2-propylamine at 0 - 25℃;	100%

: 1121-60-4
pyridine-2-carbaldehyde

: 585-32-0
2-phenyl-2-propylamine

: (E)-N-(2-phenylpropan-2-yl)-1-(pyridin-2-yl)methanimine

Conditions

Conditions	Yield
In toluene Reflux; Inert atmosphere; Dean-Stark;	100%

: 1122-72-1
6-methyl-2-pyridinecarboxaldehyde

: 585-32-0
2-phenyl-2-propylamine

: (E)-1-(6-methylpyridin-2-yl)-N-(2-phenylpropan-2-yl)methanimine

Conditions

Conditions	Yield
In toluene Reflux; Inert atmosphere; Dean-Stark;	100%

: 5470-96-2
quinoline 2-carbaldehyde

: 585-32-0
2-phenyl-2-propylamine

: (E)-N-(2-phenylpropan-2-yl)-1-(quinolin-2-yl)methanimine

Conditions

Conditions	Yield
In toluene Reflux; Inert atmosphere; Dean-Stark;	100%

: 4530-20-5
BOC-glycine

: 585-32-0
2-phenyl-2-propylamine

: 623943-92-0
[(1-methyl-1-phenylethylcarbamoyl)methyl]carbamic acid tert-butyl ester

Conditions

Conditions	Yield
Stage #1: BOC-glycine With benzotriazol-1-ol; dicyclohexyl-carbodiimide In chloroform at 20℃; for 0.166667h; Stage #2: 2-phenyl-2-propylamine In chloroform at 20℃; for 18h; Further stages.;	99%

: butyl glyoxylate monohydrate

: 585-32-0
2-phenyl-2-propylamine

: butyl (E)-2-[1-methyl-1-phenylethylimino]ethanoate

Conditions

Conditions	Yield
In benzene for 2h; Reflux; Inert atmosphere;	99%

: 1-[(4-tert-butyldiphenylsilyloxy)-5-fluoropentyl]-1H-indazole-3-carboxylic acid

: 585-32-0
2-phenyl-2-propylamine

: 1-[4-(tert-butyldiphenylsilyloxy)-5-fluoropentyl]-N-(2-phenylpropan-2-yl)-1H-indazole-3-carboxamide

Conditions

Conditions	Yield
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 24h; Inert atmosphere;	99%

: 4052-92-0
3-chlorosulfonylbenzoyl dichloride

: 585-32-0
2-phenyl-2-propylamine

: 911030-55-2
3-(1-methyl-1-phenyl-ethylcarbamoyl)-benzenesulfonyl chloride

Conditions

Conditions	Yield
2,6-dimethylpyridine In dichloromethane at 0 - 20℃; for 4h;	98%

: 154283-78-0
chloro(9H-fluoren-9-yl)dimethylsilane

: 585-32-0
2-phenyl-2-propylamine

: C24H27NSi

Conditions

Conditions	Yield
Stage #1: 2-phenyl-2-propylamine With n-butyllithium In diethyl ether; hexane at 0 - 20℃; for 4h; Inert atmosphere; Schlenk technique; Stage #2: chloro(9H-fluoren-9-yl)dimethylsilane In diethyl ether; hexane at 0 - 20℃; Inert atmosphere; Schlenk technique;	98%

: 98-09-9
benzenesulfonyl chloride

: 585-32-0
2-phenyl-2-propylamine

: 66898-01-9
N-(2-phenylpropan-2-yl)benzenesulfonamide

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0℃;	97%
With triethylamine In dichloromethane at 0 - 20℃; Inert atmosphere;	88%
With sodium hydroxide

: 3739-38-6
3-phenoxybenzoic acid

: 585-32-0
2-phenyl-2-propylamine

: 913389-91-0
3-phenoxy-N-(1-methyl-1-phenylethyl)benzamide

Conditions

Conditions	Yield
Stage #1: 3-phenoxybenzoic acid With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide for 0.0833333h; Cooling; Stage #2: 2-phenyl-2-propylamine In N,N-dimethyl-formamide at 20℃; for 2h;	97%

: 933-88-0
ortho-toluoyl chloride

: 585-32-0
2-phenyl-2-propylamine

: 249764-74-7
2-methyl-N-(2-phenylpropan-2-yl)benzamide

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0 - 20℃; for 12h; Inert atmosphere; Schlenk technique;	97%
With triethylamine In dichloromethane at 0 - 20℃; for 12h; Inert atmosphere; Schlenk technique;	97%

: 931-53-3
Cyclohexyl isocyanide

: 585-32-0
2-phenyl-2-propylamine

: 1-cyclohexyl-3-(2-phenylpropan-2-yl)thiourea

Conditions

Conditions	Yield
With sulfur at 50℃; for 16h;	97%

: C23H29ClSi

: 585-32-0
2-phenyl-2-propylamine

: C32H41NSi

Conditions

Conditions	Yield
Stage #1: 2-phenyl-2-propylamine With n-butyllithium In diethyl ether; hexane at 0 - 20℃; for 3h; Inert atmosphere; Schlenk technique; Stage #2: C23H29ClSi In diethyl ether; hexane at 0 - 20℃; Inert atmosphere; Schlenk technique;	97%

: 3972-56-3
4-(tert-butyl)chlorobenzene

: 585-32-0
2-phenyl-2-propylamine

: 4-(tert-butyl)-N-(2-phenylpropan-2-yl)aniline

Conditions

Conditions	Yield
With 2,6-di-tert-butyl-4-methyl-phenol; [1,3-bis(2,6-diisopentylphenyl)-4,5-dichloroimidazol-2-ylidene](3-chloropyridyl)palladium(II) dichloride; sodium hydride In 1,2-dimethoxyethane at 80℃; for 24h; Sealed tube; Inert atmosphere; Schlenk technique;	97%

: 618-46-2
m-Chlorobenzoyl chloride

: 585-32-0
2-phenyl-2-propylamine

: 866766-98-5
3-chloro-N-(1-methyl-1-phenylethyl)benzamide

Conditions

Conditions	Yield
With dmap; triethylamine In dichloromethane at 20℃; for 3h;	96%

: 76966-07-9
1,4-dihydro-1-naphthoyl chloride

: 585-32-0
2-phenyl-2-propylamine

: 101507-17-9
N-(alpha,alpha-dimethylbenzyl)-1,4-dihydro-alpha-naphthoamide

Conditions

Conditions	Yield
With triethylamine In water	95.5%

: 98-59-9
p-toluenesulfonyl chloride

: 585-32-0
2-phenyl-2-propylamine

: 66898-03-1
N-(α,α-dimethylbenzyl)-p-toluenesulfonamide

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0℃;	95%
With sodium hydroxide

: 585-32-0
2-phenyl-2-propylamine

: 300561-19-7
N-acetyl-N-(2,3,4,5,6-pentafluorophenyl)methanesulfonamide

: 79649-68-6
N-(1-methyl-1phenylethyl)acetamide

Conditions

Conditions	Yield
In tetrahydrofuran at 50℃; for 36h; Acylation;	95%

: 33581-95-2
tert-butylsulfamyl chloride

: 585-32-0
2-phenyl-2-propylamine

: N-cumyl-N'-t-butylsulfamide

Conditions

Conditions	Yield
In diethyl ether; hexane at 20℃; for 1.5h;	95%

: 585-32-0
2-phenyl-2-propylamine

3-halopyridine: 3-halopyridine

: N-(2-phenylpropan-2-yl)pyridin-3-amine

Conditions

Conditions	Yield
With 2,6-di-tert-butyl-4-methyl-phenol; [1,3-bis(2,6-diisopentylphenyl)-4,5-dichloroimidazol-2-ylidene](3-chloropyridyl)palladium(II) dichloride; sodium hydride In 1,2-dimethoxyethane at 80℃; for 24h; Sealed tube; Inert atmosphere; Schlenk technique;	95%

: 368-43-4
phenylsulfonyl fluoride

: 585-32-0
2-phenyl-2-propylamine

: 66898-01-9
N-(2-phenylpropan-2-yl)benzenesulfonamide

Conditions

Conditions	Yield
With 1,1,3,3-Tetramethyldisiloxane; benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine In dimethyl sulfoxide at 25℃; for 24h; Sealed tube;	95%

: 4-(tert-butyl)benzene-1-sulfonyl fluoride

: 585-32-0
2-phenyl-2-propylamine

: 4-(tert-butyl)-N-(2-phenylpropan-2-yl)benzenesulfonamide

Conditions

Conditions	Yield
With 1,1,3,3-Tetramethyldisiloxane; benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine In dimethyl sulfoxide at 25℃; for 24h; Sealed tube;	95%

: 29336-30-9, 86512-66-5
2-bromo-3,3-dimethylbutanoyl chloride

: 585-32-0
2-phenyl-2-propylamine

: 74712-19-9
bromobutide

Conditions

Conditions	Yield
With 1-methyl-1H-imidazole; N,N,N,N,-tetramethylethylenediamine; potassium carbonate In chlorobenzene at 20 - 25℃; for 2h;	94%
With triethylamine In benzene for 4h; Ambient temperature; Yield given;
In tetrachloromethane; dichloromethane Yield given;

2-Phenylpropan-2-amine Specification

This chemical is called 2-Phenylpropan-2-amine, and it can also be named as (Phenylisopropyl)amine. With the molecular formula of C₉H₁₃N, its molecular weight is 135.21. The CAS registry number of this chemical is 585-32-0.

Other characteristics of the 2-Phenylpropan-2-amine can be summarised as followings: (1)ACD/LogP: 2.13; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 7.4): 0.192; (4)ACD/BCF (pH 5.5): 1; (5)ACD/BCF (pH 7.4): 1; (6)ACD/KOC (pH 5.5): 1; (7)ACD/KOC (pH 7.4): 3.966; (8)#H bond acceptors: 1; (9)#H bond donors: 2; (10)#Freely Rotating Bonds: 2; (11)Polar Surface Area: 26.02 Å²; (12)Index of Refraction: 1.52; (13)Molar Refractivity: 43.542 cm³; (14)Molar Volume: 143.292 cm³; (15)Polarizability: 17.262×10^-24cm³; (16)Surface Tension: 33.434 dyne/cm; (17)Density: 0.944 g/cm³; (18)Flash Point: 84.05 °C; (19)Enthalpy of Vaporization: 43.27 kJ/mol; (20)Boiling Point: 196.499 °C at 760 mmHg; (21)Vapour Pressure: 0.397 mmHg at 25°C.

Production method of this chemical: The 2-Phenylpropan-2-amine could be obtained by the reactant of 2-azido-2-phenylpropane. This reaction needs the reagent of LiAlH₄, and the solvent of diethyl ether. The other condition is heating.

Uses of this chemical: The (a-nitro-isopropyl)-benzene could be obtained by the reactant of 2-Phenylpropan-2-amine. This reaction needs the reagent of KMnO_4.

When you are using this chemical, please be cautious about it as the following: This chemical is irritating to eyes, respiratory system and skin. You should wear suitable protective clothing when you use it. In case of contacting with eyes, rinse immediately with plenty of water and seek medical advice.

You can still convert the following datas into molecular structure:
1.SMILES: CC(C)(c1ccccc1)N
2.InChI: InChI=1/C9H13N/c1-9(2,10)8-6-4-3-5-7-8/h3-7H,10H2,1-2H3
3.InChIKey: KDFDOINBXBEOLZ-UHFFFAOYAK

Product Name

CUMYLAMINE

Synthetic route

2-Phenylpropan-2-amine Specification

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