CAS No.124-40-3,Dimethylamine Suppliers

Lonwin Chemical Group Limited

Dimethylamine CAS：124-40-3 Specification low price and high purity Welcome to contact us to get complete COA. Shanghai Lonwin Chemical Co.,Ltd is a leading manufacturer and supplier of chemicals in China.We develop,produce and distribute high

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Cas:124-40-3

Min.Order:1 Kilogram

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Type:Other

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Hunan Russell Chemicals Technology Co.,Ltd

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Dimethylamine solution, 40 wt. % in water 124-40-3

Cas:124-40-3

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Synthetic route

: 62-75-9
N-Nitrosodimethylamine

: 124-40-3
dimethyl amine

Conditions

Conditions	Yield
With iron; nickel In water pH=6.3 - 9.2; Kinetics; Further Variations:; Reagents; Hydrogenation;	100%
With isocyanate de chlorosulfonyle In diethyl ether for 10h; Ambient temperature;	65%
With titanium(III) chloride; water

: 85809-41-2
3-ethynyl-cyclohepta-1.3.5-triene

: 993-50-0
(dimethylamino)trimethyltin

A: 286387-63-1
3-(trimethylstannylethynyl)-1,3,5-cycloheptatriene

B: 124-40-3
dimethyl amine

Conditions

Conditions	Yield
In neat (no solvent) Me3SnNMe2 added to 3-ethynyl-1,3,5-cycloheptatriene, react. mixture stirred without a solvent for 5 min at ambient temp., Me2NH evapd.; Me2NH evapd., product isolated in quant. yield;	A 100% B n/a

...Expand

: 68-12-2, 33513-42-7
N,N-dimethyl-formamide

: 100-46-9
benzylamine

A: 6343-54-0
N-benzylformamide

B: 124-40-3
dimethyl amine

Conditions

Conditions	Yield
With 2,3-dihydrophthalazine-1,4-dione at 80 - 95℃; for 40h;	A 99% B n/a
With cerium(IV) oxide at 100℃; for 12h; Reagent/catalyst;

...Expand

: C13H23N3O3S

: 68-12-2, 33513-42-7
N,N-dimethyl-formamide

A: C15H23N3O5S

B: 124-40-3
dimethyl amine

Conditions

Conditions	Yield
With 2,3-dihydrophthalazine-1,4-dione at 80 - 95℃; for 40h;	A 98% B n/a

...Expand

: 39139-79-2
1-dimethylamino-2,4-dinitronaphthalene

: 75-04-7
ethylamine

A: 27210-67-9
N-ethyl-2,4-dinitro-1-naphthylamine

B: 124-40-3
dimethyl amine

Conditions

Conditions	Yield
In water at 30℃; for 2h;	A 98% B n/a

...Expand

: 107-10-8
propylamine

: 71240-22-7
2-(1H-benzoimidazol-2-yl)-3-dimethylamino-acrylic acid ethyl ester

A: 124-40-3
dimethyl amine

B: (E)-2-(1H-Benzoimidazol-2-yl)-3-propylamino-acrylic acid ethyl ester

Conditions

Conditions	Yield
at 40℃; for 0.5h; Irradiation;	A n/a B 98%

...Expand

: 33966-50-6
SEC-BUTYLAMINE

: 71240-22-7
2-(1H-benzoimidazol-2-yl)-3-dimethylamino-acrylic acid ethyl ester

A: 124-40-3
dimethyl amine

B: (E)-2-(1H-Benzoimidazol-2-yl)-3-sec-butylamino-acrylic acid ethyl ester

Conditions

Conditions	Yield
at 60℃; for 0.5h; Irradiation;	A n/a B 98%

...Expand

: 506-59-2
N,N-dimethylammonium chloride

: 124-40-3
dimethyl amine

Conditions

Conditions	Yield
With potassium hydroxide In water Inert atmosphere;	98%
With potassium hydroxide In dichloromethane at -15 - -5℃; for 1h;	90%
With potassium hydroxide Alkaline conditions;

: 29882-02-8
N',N''-dicyclohexyl-N,N-dimethylguanidine

: 108-91-8
cyclohexylamine

A: 4833-41-4
N,N',N''-tricyclohexylguanidine

B: 124-40-3
dimethyl amine

Conditions

Conditions	Yield
With [ς:η1:η5-(OCH2)(Me2CH2)C2B9H9]Ti(NMe2) at 110 - 115℃;	A 98% B n/a

...Expand

: 71240-24-9
2-benzooxazol-2-yl-3-dimethylamino-acrylic acid ethyl ester

: 75-64-9
tert-butylamine

A: 124-40-3
dimethyl amine

B: (E)-2-Benzooxazol-2-yl-3-tert-butylamino-acrylic acid ethyl ester

Conditions

Conditions	Yield
at 40℃; for 0.5h; Irradiation;	A n/a B 97%

...Expand

: 75-64-9
tert-butylamine

: 71240-22-7
2-(1H-benzoimidazol-2-yl)-3-dimethylamino-acrylic acid ethyl ester

A: 124-40-3
dimethyl amine

B: (E)-2-(1H-Benzoimidazol-2-yl)-3-tert-butylamino-acrylic acid ethyl ester

Conditions

Conditions	Yield
at 40℃; for 0.5h; Irradiation;	A n/a B 97%

...Expand

: 1198-55-6
o-chloranil

: 1608-26-0
Hexamethylphosphorous triamide

A: 124-40-3
dimethyl amine

B: 320747-63-5
tetrachlorobenzo<1,3,2>dioxaphosphol-2-yl-dimethylamine

Conditions

Conditions	Yield
With ammonium chloride In toluene for 1.5h; Heating;	A n/a B 97%

...Expand

: 123-75-1
pyrrolidine

: 29882-02-8
N',N''-dicyclohexyl-N,N-dimethylguanidine

A: 60006-28-2
N,N'-dicyclohexylpyrrolidine-1-carboximidamide

B: 124-40-3
dimethyl amine

Conditions

Conditions	Yield
With [ς:η1:η5-(OCH2)(Me2CH2)C2B9H9]Ti(NMe2) at 110 - 115℃;	A 97% B n/a

...Expand

: 29882-02-8
N',N''-dicyclohexyl-N,N-dimethylguanidine

: 75-31-0
isopropylamine

A: N,N'-Dicyclohexyl-N''-isopropyl-guanidin

B: 124-40-3
dimethyl amine

Conditions

Conditions	Yield
With [ς:η1:η5-(OCH2)(Me2CH2)C2B9H9]Ti(NMe2) at 110 - 115℃;	A 97% B n/a

...Expand

: 5815-08-7
tert-Butoxybis(dimethylamino)methane

: 74119-34-9
3-Dimethylamino-2-(formylaminomethyl)acrylsaeure-ethylester

A: 924-99-2, 1117-37-9, 114894-59-6
ethyl 3-(dimethylamino)acrylate

B: 124-40-3
dimethyl amine

C: 75-65-0
tert-butyl alcohol

Conditions

Conditions	Yield
at 160℃; for 3h;	A 96% B n/a C n/a

...Expand

: 110-89-4
piperidine

: 29882-02-8
N',N''-dicyclohexyl-N,N-dimethylguanidine

A: 60006-25-9
N,N'-dicyclohexylpiperidine-1-carboximidamide

B: 124-40-3
dimethyl amine

Conditions

Conditions	Yield
With [ς:η1:η5-(OCH2)(Me2CH2)C2B9H9]Ti(NMe2) at 110 - 115℃;	A 96% B n/a

...Expand

: 75712-80-0
N,N-dimethylhexa-1,5-dien-3-amine

A: 764-59-0
hex-5-en-1-al

B: 82574-98-9
(E)-N,N-Dimethyl-1,5-hexadien-1-amin

C: 124-40-3
dimethyl amine

Conditions

Conditions	Yield
at 223.5℃; for 12h;	A n/a B 95.8% C n/a
at 160.2 - 200.1℃; Yield given. Yields of byproduct given;
With N,N-dimethyl-cyclohexanamine at 160.2 - 200.1℃; under 3 Torr; Kinetics; Thermodynamic data; Cope rearrengament, ΔH, ΔG, ΔS*, Ea;

...Expand

: 116018-88-3
((CH3)2N)2PH(Fe(CO)4)

: 103616-27-9
(PPh4)(hydridoiron(carbonyl)4)

A: ((CH3)2N)PH(Fe(CO)4)2(1-)*(C6H5)4P(1+)={(C6H5)4P}{(CH3)2NPH(Fe(CO)4)2}

B: 124-40-3
dimethyl amine

Conditions

Conditions	Yield
	A 95% B n/a

...Expand

: 87-52-5
3-(Dimethylaminomethyl)indole

: 75-04-7
ethylamine

A: 57506-90-8
3-(N-ethylamino)methylindole

B: 124-40-3
dimethyl amine

Conditions

Conditions	Yield
Heating;	A 94% B n/a

...Expand

: 75-31-0
isopropylamine

: 71240-22-7
2-(1H-benzoimidazol-2-yl)-3-dimethylamino-acrylic acid ethyl ester

A: 124-40-3
dimethyl amine

B: (E)-2-(1H-Benzoimidazol-2-yl)-3-isopropylamino-acrylic acid ethyl ester

Conditions

Conditions	Yield
at 30℃; for 0.5h; Irradiation;	A n/a B 94%

...Expand

: 75-31-0
isopropylamine

: 68897-42-7
N′,N″-diisopropyl-N,N-dimethyl guanidine

A: 121948-77-4
N,N', N''-tri(isopropyl)guanidine

B: 124-40-3
dimethyl amine

Conditions

Conditions	Yield
With [ς:η1:η5-(OCH2)(Me2CH2)C2B9H9]Ti(NMe2) at 110 - 115℃;	A 94% B n/a

...Expand

: 38353-77-4
N-(N3-p-toluenesulfonyl)-3-aminopropylphthalimide

: 68-12-2, 33513-42-7
N,N-dimethyl-formamide

A: 1445-69-8
2,3-dihydrophthalazine-1,4-dione

B: 107976-50-1
N1-formyl-N3-tosyl-1,3-propanediamine

C: 124-40-3
dimethyl amine

Conditions

Conditions	Yield
With hydrazine hydrate at 80℃; for 3h;	A n/a B 93% C n/a

...Expand

: 71240-23-8
ethyl (2E/Z)-2-(1,3-benzothiazol-2-yl)-3-(dimethylamino)acrylate

: 107-10-8
propylamine

A: 124-40-3
dimethyl amine

B: (Z)-2-Benzothiazol-2-yl-3-propylamino-acrylic acid ethyl ester

Conditions

Conditions	Yield
at 40℃; for 0.5h; Irradiation;	A n/a B 93%

...Expand

: 1630-79-1
tetrakis(dimethylamido)diborane

: 109-73-9
N-butylamine

A: 7360-73-8
tetrakis(n-butylamino)diborane(4)

B: 124-40-3
dimethyl amine

Conditions

Conditions	Yield
In hexane heating from 76 to 174°C during 21.6 h;	A 93% B n/a
4 equiv. n-C4H9NH2, slow react. at room temp.;
4 equiv. n-C4H9NH2, slow react. at room temp.;

...Expand

: 58369-78-1
(2-bromoethyl)dimethyl-(3,3-dimethylallyl)ammonium bromide

: 107-11-9
1-amino-2-propene

A: 88019-80-1
Allyl-[3,3-dimethyl-pent-4-en-(E)-ylidene]-amine

B: 124-40-3
dimethyl amine

Conditions

Conditions	Yield
With potassium hydroxide In water at 90 - 95℃; for 1h;	A 92.7% B 79.5%
With potassium hydroxide In water at 90 - 95℃; for 1h; Product distribution; ratio of reactants;	A 92.7% B 79.5%

...Expand

: 108-91-8
cyclohexylamine

: 68897-42-7
N′,N″-diisopropyl-N,N-dimethyl guanidine

A: 124-40-3
dimethyl amine

B: 2-Cyclohexyl-1,3-diisopropylguanidine

Conditions

Conditions	Yield
With [ς:η1:η5-(OCH2)(Me2CH2)C2B9H9]Ti(NMe2) at 110 - 115℃;	A n/a B 92%

...Expand

: 87-52-5
3-(Dimethylaminomethyl)indole

: 108-91-8
cyclohexylamine

A: 53924-03-1
N-indol-3-ylmethylcyclohexylamine

B: 124-40-3
dimethyl amine

Conditions

Conditions	Yield
Heating;	A 91% B n/a

...Expand

: 552-79-4, 1201-56-5, 14222-20-9, 17605-71-9, 39263-91-7, 42151-56-4, 51018-28-1, 62560-55-8, 87040-40-2
(+/-)-erythro-methylephedrine

A: 50-00-0
formaldehyd

: 90-81-3, 90-82-4, 299-42-3, 321-97-1, 321-98-2, 4125-58-0, 34783-90-9, 38732-95-5, 53214-57-6
ephedrine

C: 100-52-7
benzaldehyde

D: 75-07-0
acetaldehyde

E: 124-40-3
dimethyl amine

Conditions

Conditions	Yield
With water at 25℃; Product distribution; Mechanism; anodic oxidation, carbonate buffer, pH 10; effect of substituents investigated with different types of β-alkanolamines;	A 6.4% B 0.5% C 91% D 90% E 91%

...Expand

: 57-14-7
1,1-dimethylhydrazine

: 135-19-3
β-naphthol

A: 2834-92-6
1-amino-2-naphthol

B: 124-40-3
dimethyl amine

Conditions

Conditions	Yield
at 80℃; for 4h;	A 91% B n/a

...Expand

: 58369-78-1
(2-bromoethyl)dimethyl-(3,3-dimethylallyl)ammonium bromide

: 62-53-3
aniline

A: 88019-86-7
[3,3-Dimethyl-pent-4-en-(E)-ylidene]-phenyl-amine

B: 124-40-3
dimethyl amine

Conditions

Conditions	Yield
With potassium hydroxide In water at 90 - 95℃; for 1h;	A 90.9% B 84.9%

...Expand

: 558-30-5
2-methyl-1,2-epoxypropane

: 124-40-3
dimethyl amine

: 14123-48-9
1-dimethylamino-2-methyl-propan-2-ol

Conditions

Conditions	Yield
In water at -5 - 20℃; Schlenk technique; Inert atmosphere; Sealed tube;	100%
With water In water at 20 - 50℃; for 120h; Sealed tube;	91%
In water at 20℃; for 12h; Cooling with ice; Inert atmosphere;	89%

: 6684-39-5
2-chloropyridine-5-sulfonyl chloride

: 124-40-3
dimethyl amine

: 52480-31-6
6-chloro-N,N-dimethylpyridine-3-sulfonamide

Conditions

Conditions	Yield
With triethylamine In tetrahydrofuran at 20℃; for 2h;	100%
With triethylamine In tetrahydrofuran at 20℃; for 0.5h;	95%
With triethylamine In tetrahydrofuran at 20℃; for 0.5h;	95%

: 4101-68-2
1,10-dibromodecane

: 124-40-3
dimethyl amine

: 1938-62-1
N,N,N',N'-tetramethyl-1,10-diaminodecane

Conditions

Conditions	Yield
In chloroform at 20℃; for 24h;	100%
With sodium carbonate In ethanol; water for 24h; Heating;	92%
With ethanol
In benzene at 4 - 5℃;
at 4 - 5℃;

: 543-20-4
succinoyl dichloride

: 124-40-3
dimethyl amine

: 7334-51-2
N,N,N',N'-tetramethylsuccinamide

Conditions

Conditions	Yield
In water at 0℃; for 0.5h;	100%
In diethyl ether at -78 - 20℃;	91%
In dichloromethane; water at 0 - 20℃; for 20h; Inert atmosphere;	81%
With diethyl ether
In water at 0℃; for 0.5h;

: 629-03-8
1 ,6-dibromohexane

: 124-40-3
dimethyl amine

: 111-18-2
N,N,N',N'-tetramethylhexamethylenediamine

Conditions

Conditions	Yield
In tetrahydrofuran at 0 - 20℃; for 24h;	100%
In chloroform at 20℃; for 24h;	100%
With sodium carbonate In ethanol; water for 24h; Heating;	98%

: 81-25-4
cholic acid

: 124-40-3
dimethyl amine

: 86678-85-5
(R)-N,N-dimethyl-4-((3R,5S,7R,8R,9S,10S,12S,13R,14S,17R)-3,7,12-trihydroxy-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthrene-17-yl)valeramide

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In N,N-dimethyl-formamide at 20℃; for 16h; Inert atmosphere;	100%
With tributyl-amine; chloroformic acid ethyl ester In 1,4-dioxane 10 deg C, 30 min then rt., 2 h;	78%
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In dichloromethane at 20℃; for 10h;	74.2%
With water at 250℃;
With tributyl-amine; chloroformic acid ethyl ester Multistep reaction;

: 124-40-3
dimethyl amine

: 106-93-4
ethylene dibromide

: 110-18-9
N,N,N,N,-tetramethylethylenediamine

Conditions

Conditions	Yield
In tetrahydrofuran at 0 - 20℃; for 24h;	100%
In chloroform at 20℃; for 24h;	100%

: 124-40-3
dimethyl amine

: 922-67-8
propynoic acid methyl ester

: 999-59-7
methyl 3-(N,N-dimethylamino)-2-propenoate

Conditions

Conditions	Yield
In diethyl ether at 20℃; for 1h;	100%
With benzene

: 124-40-3
dimethyl amine

: 98-59-9
p-toluenesulfonyl chloride

: 599-69-9
N,N,4-trimethylbenzenesulfonamide

Conditions

Conditions	Yield
With triethylamine In tetrahydrofuran at 25℃; for 1h;	100%
	99%
With cesium fluoride supported on Celite at 50℃; for 0.75h; chemoselective reaction;	91%

: 124-40-3
dimethyl amine

: 62-75-9
N-Nitrosodimethylamine

Conditions

Conditions	Yield
With sulfuric acid; silica gel; sodium nitrite In dichloromethane at 20℃; for 0.5h; Nitrosation;	100%
With Nafion-H(R); silica gel; sodium nitrite In dichloromethane at 20℃; for 0.166667h;	100%
With trichloromelamine; silica gel; sodium nitrite In dichloromethane; water at 20℃; for 0.0333333h;	100%

: 615-18-9
2-chloro-1,3-benzoxazole

: 124-40-3
dimethyl amine

: 13858-89-4
2-dimethylaminobenzoxazole

Conditions

Conditions	Yield
In tetrahydrofuran; water for 0.166667h; Inert atmosphere; Reflux;	100%
In water at 20℃; for 1h;	90%
In water at 20℃; for 5h; Green chemistry;	71%

: 100-47-0
benzonitrile

: 124-40-3
dimethyl amine

: 20548-18-9, 39116-58-0
N,N-Dimethyl-benzamidine

Conditions

Conditions	Yield
Stage #1: dimethyl amine With n-butyllithium In diethyl ether; hexane at -20℃; for 0.166667h; Stage #2: benzonitrile at -20℃; for 1h;	100%

: 873-51-8
phenylborondichloride

: 124-40-3
dimethyl amine

: 1201-45-2
Bis-(dimethylamino)-phenylboran

Conditions

Conditions	Yield
In pentane at -78 - 20℃; Inert atmosphere;	100%
In hexane	87%
In hexane	87%

: 4044-65-9
1 ,4-phenylenediisothiocyanate

: 124-40-3
dimethyl amine

: 16349-56-7
3-[4-(3,3-dimethyl-thioureido)-phenyl]-1,1-dimethyl-thiourea

Conditions

Conditions	Yield
at 20℃; under 750.06 Torr; Addition; solid-gas reaction;	100%

: 124-40-3
dimethyl amine

: 102-92-1
Cinnamoyl chloride

: 17431-39-9
(E)-N,N-dimethylcinnamamide

Conditions

Conditions	Yield
In water at 0℃; for 0.75h;	100%
In methanol for 15h; Ambient temperature;	81%
In diethyl ether for 0.5h;	46.9%

: 124-40-3
dimethyl amine

: 10199-89-0
NBD chloride

: 1455-87-4
N,N-dimethyl-7-nitrobenzo[c][1,2,5]oxadiazol-4-amine

Conditions

Conditions	Yield
In methanol	100%
In dichloromethane at 20℃; for 2h;	98%
With triethylamine In dichloromethane; water at 20℃; for 1.5h;	52.7%
In ethanol
In water; ethyl acetate 1.) 0 deg C, 30 min, 2.) r.t., 2 h;

: 124-40-3
dimethyl amine

: 645-45-4
hydrocinnamic acid chloride

: 5830-31-9
N,N-dimethyl-3-phenylpropanamide

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0 - 20℃; for 14h; Inert atmosphere;	100%
With triethylamine In diethyl ether	93%
With triethylamine In diethyl ether Inert atmosphere;	93%

: 2930-05-4
Benzyloxymethyl-oxiran

: 124-40-3
dimethyl amine

: 97807-83-5
(+/-)-dimethyl<2-hydroxy-3-(benzyloxy)propyl>amine

Conditions

Conditions	Yield
In tetrahydrofuran; water for 2h; Heating;	100%

: 5247-85-8
1,8-naphtholactone

: 124-40-3
dimethyl amine

: 69674-57-3
N,N-Dimethyl-8-hydroxy-naphthalin-1-carboxamid

Conditions

Conditions	Yield
In toluene Heating;	100%

: 1973-09-7
6-chloro-N,N'-diphenyl-1,3,5-triazine-2,4-diamine

: 124-40-3
dimethyl amine

: 7710-42-1
N,N’-diphenyl-6-(isopropylamino)-[1,3,5]triazine-2,4-diamine

Conditions

Conditions	Yield
With water; sodium carbonate for 1.5h; Heating;	100%

: 52813-87-3
ethylthio-8 methyl-5 5H-dibenzazepine-10-acetate de nitro-4 phenyle

: 124-40-3
dimethyl amine

: 52813-88-4
ethylthio-8 trimethyl-N,N,5 5H-dibenzazepine-10-acetamide

Conditions

Conditions	Yield
In chloroform for 1h; Ambient temperature;	100%

: 933-88-0
ortho-toluoyl chloride

: 124-40-3
dimethyl amine

: 6639-19-6
N,N,2-trimethylbenzamide

Conditions

Conditions	Yield
	100%
In water; toluene
In diethyl ether at 20℃; for 16h;

: 28735-24-2
5-methyl-3-(methylsulfanyl)-1,2,4-triazine

: 124-40-3
dimethyl amine

: 115125-15-0
N,N,5-trimethyl-1,2,4-triazin-3-amine

Conditions

Conditions	Yield
In water a.) RT, 12 h b.) 70 deg C, 30 min;	100%

: 50-00-0
formaldehyd

: 67720-26-7
6,7,8,9-tetrahydrobenzoindole

: 124-40-3
dimethyl amine

: 110595-87-4
3-dimethylaminomethyl-6,7,8,9-tetrahydrobenzoindole

Conditions

Conditions	Yield
In acetic acid at 80℃; for 0.166667h;	100%

...Expand

: 50-00-0
formaldehyd

: 124-40-3
dimethyl amine

: 155330-95-3
1,3-Bis(3-thienyloxy)propane

: {3-[3-(2-Dimethylaminomethyl-thiophen-3-yloxy)-propoxy]-thiophen-2-ylmethyl}-dimethyl-amine

Conditions

Conditions	Yield
With acetic acid Mannich reaction; Heating;	100%
With acetic acid

...Expand

: 50-00-0
formaldehyd

: 124-40-3
dimethyl amine

: 155330-77-1
C14H18O4S2

: [3-(2-{2-[2-(2-Dimethylaminomethyl-thiophen-3-yloxy)-ethoxy]-ethoxy}-ethoxy)-thiophen-2-ylmethyl]-dimethyl-amine

Conditions

Conditions	Yield
With acetic acid at 20℃; for 48h; Mannich reaction;	100%
With acetic acid

...Expand

: 50-00-0
formaldehyd

: 124-40-3
dimethyl amine

: 172226-45-8
(+/-)-3-<<(1,1-dimethylethyl)dimethylsilyl>oxy>-4,4-dimethyl-3,4-dihydro-2H,10H-<1,4>dioxepino<2,3-g>indole

: 172226-24-3
(+/-)-3-<<(1,1-dimethylethyl)dimethylsilyl>oxy>-4,4-dimethyl-8-<(N,N-dimethylamino)methyl>-3,4-dihydro-2H,10H-<1,4>dioxepino<2,3-g>indole