CAS No.529-17-9,8-METHYL-8-AZABICYCLO[3.2.1]OCTANE Suppliers

Henan Tianfu Chemical Co., Ltd.

High Quality Best price Fast Delivery Good Service Welcome to Henan Tianfu Chemical Co., Ltd. website. Our company engages in Sodium Tripolyphosphate (STPP) and Sodium Hexametabphosphate (SHMP) production; developm

N-Methyl-8-azabicyclo[3.2.1]octane

Cas:529-17-9

Min.Order:1 Kilogram

Negotiable

Type:Lab/Research institutions

inquiry

Shanghai Upbio Tech Co.,Ltd

1.In No Less 10 years exporting experience. you can 100% received goods 2.Lower Price with higher quality 3,Free sample 4,We are sincerely responsible for the "product quality" and "After Service" Upbio is Specializ

8-Azabicyclo[3.2.1]octane,8-methyl-

Cas:529-17-9

Min.Order:1 Gram

Negotiable

Type:Lab/Research institutions

inquiry

Hangzhou Keyingchem Co.,Ltd

Hangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det

8-METHYL-8-AZABICYCLO[3.2.1]OCTANE

Cas:529-17-9

Min.Order:0 Metric Ton

Negotiable

Type:Lab/Research institutions

inquiry

Shandong Mopai Biotechnology Co., LTD

Shandong Mopai Biotechnology Co., LTD is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemicals. W

8-Azabicyclo[3.2.1]octane,8-methyl-

Cas:529-17-9

Min.Order:1 Gram

Negotiable

Type:Lab/Research institutions

inquiry

Henan Allgreen Chemical Co.,Ltd

high quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea

8-METHYL-8-AZABICYCLO[3.2.1]OCTANE

Cas:529-17-9

Min.Order:0

Negotiable

Type:Manufacturers

inquiry

Antimex Chemical Limied

hight degree of purity Application:Fine chemical intermediates, used as the main raw material for he synthesis of various pesticides, medicines, surfactants, polymer monomers, Ond Ontifungal agents

8-Azabicyclo[3.2.1]octane,8-methyl-

Cas:529-17-9

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

ZHEJIANG JIUZHOU CHEM CO.,LTD

factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin

8-METHYL-8-AZABICYCLO[3.2.1]OCTANE

Cas:529-17-9

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Finetech Industry Limited

FINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the 8-METHYL-8-AZABICYCLO[3.2.1]OCTANE, CAS:529-17-9 with the most competitive price and

8-METHYL-8-AZABICYCLO[3.2.1]OCTANE

Cas:529-17-9

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Topbatt Chemical Co., Ltd.

Topbatt Chemical Co., Ltd., Established in 2019, located in Shenzhen, Guangdong Province, is a Manufacturer and Trading company which specialized in fine chemicals like Pharmaceutical Reference Standards and Stable Isotopes. Our Stable Isotopes produ

Tropane

Cas:529-17-9

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Synthetic route

: 532-24-1
tropinone

: 529-17-9
tropane

Conditions

Conditions	Yield
With hydrogenchloride; hydrogen; platinum(IV) oxide under 1.5 Torr; for 35h;	100%
With potassium hydroxide; hydrazine In 2,2'-[1,2-ethanediylbis(oxy)]bisethanol for 8h; Wolff-Kischener reduction; Heating;

: 201230-82-2
carbon monoxide

: 529-18-0
tropidine

A: 529-17-9
tropane

B: 68969-37-9
tropan-2-yl-methanol

C: 90949-82-9, 888716-28-7
3-hydroxymethyl-8-methyl-8-azabicyclo[3.2.1]octane

D: 93047-52-0, 99658-61-4
Tropan-3β-carboxaldehyd

Conditions

Conditions	Yield
With hydrogen; di-μ-chlorobis(norbornadiene)dirhodium(I); tributylphosphine In benzene at 100℃; under 60004.8 Torr; for 6h;	A 2% B n/a C n/a D 92%

...Expand

: 201230-82-2
carbon monoxide

: 529-18-0
tropidine

A: 529-17-9
tropane

B: 68969-37-9
tropan-2-yl-methanol

C: 90949-82-9, 888716-28-7
3-hydroxymethyl-8-methyl-8-azabicyclo[3.2.1]octane

D: 93047-52-0, 99658-61-4
Tropan-3β-carboxaldehyd

E: 8-Methyl-8-aza-bicyclo[3.2.1]octane-2-carbaldehyde

Conditions

Conditions	Yield
With hydrogen; carbonylhydridetris(triphenylphosphine)rhodium(I) In benzene at 100℃; under 60004.8 Torr; for 6h; Product distribution; various catalysts, formed in situ from various phosphines;	A 2% B n/a C n/a D 86% E 10%

...Expand

: 95799-01-2
N-<(benzoyloxy)carbonyl>nortropane

: 529-17-9
tropane

Conditions

Conditions	Yield
With lithium aluminium tetrahydride In tetrahydrofuran for 24h; Ambient temperature;	72%

: 122709-62-0
1-<(methyl(4-cycloheptenyl)carbamoyl)oxy>-2(1H)-pyridinethione

A: 529-17-9
tropane

B: 128729-93-1
2-(2-pyridylthio)tropane

Conditions

Conditions	Yield
With 2-methylpropan-2-thiol; acetic acid In acetonitrile at 25℃; Irradiation;	A 68% B 3 % Chromat.

: 201230-82-2
carbon monoxide

: 529-18-0
tropidine

A: 529-17-9
tropane

B: 93047-52-0, 99658-61-4
Tropan-3β-carboxaldehyd

C: 8-Methyl-8-aza-bicyclo[3.2.1]octane-2-carbaldehyde

Conditions

Conditions	Yield
With hydrogen; di-μ-chlorobis(norbornadiene)dirhodium(I); tricyclohexylphosphine In benzene at 100℃; under 60004.8 Torr; for 6h;	A 22% B 67% C 11%

...Expand

: 122709-62-0
1-<(methyl(4-cycloheptenyl)carbamoyl)oxy>-2(1H)-pyridinethione

: 529-17-9
tropane

Conditions

Conditions	Yield
With 2-methylpropan-2-thiol; acetic acid In benzene at 4℃;	67%

: 42870-65-5
N-methyl-N-cycloheptylamine

: 529-17-9
tropane

Conditions

Conditions	Yield
With chlorine Erwaermen des erhaltenen Chlor-cycloheptyl-methyl-amins mit 84%ig. wss. Schwefelsaeure;

: 529-18-0, 122709-67-5
Tropidin

: 529-17-9
tropane

Conditions

Conditions	Yield
With diethyl ether; platinum Hydrogenation;

: 120-29-6
3-tropanol

: 529-17-9
tropane

Conditions

Conditions	Yield
With phosphonium iodide; hydrogen iodide at 195 - 200℃; im Rohr;

: (1S,4R)-4-Methylamino-cycloheptanol

: 529-17-9
tropane

Conditions

Conditions	Yield
With thionyl chloride 1.) CDCl3, 0 deg C to room temperature, 19.5 h, 2.) 12 h; Yield given. Multistep reaction;

hydroscopolin: hydroscopolin

: 529-17-9
tropane

Conditions

Conditions	Yield
With phosphonium iodide; hydrogen iodide at 195 - 205℃; im Rohr;

: 103392-59-2
tropane-6,7-diol

: 10034-85-2
hydrogen iodide

phosphonium iodide: phosphonium iodide

: 529-17-9
tropane

Conditions

Conditions	Yield
at 195 - 205℃;

...Expand

: 10034-85-2
hydrogen iodide

: 120-29-6
3-tropanol

phosphonium iodide: phosphonium iodide

: 529-17-9
tropane

Conditions

Conditions	Yield
at 195 - 200℃;

...Expand

: 60-29-7
diethyl ether

: 529-18-0
tropidine

platinum black: platinum black

: 529-17-9
tropane

Conditions

Conditions	Yield
Hydrogenation;

...Expand

tropane chloromethylate: tropane chloromethylate

: 529-17-9
tropane

Conditions

Conditions	Yield
Bei der trocknen Destillation;

hydriodide of 3-iodo-tropane: hydriodide of 3-iodo-tropane

A: 529-17-9
tropane

: 529-18-0, 122709-67-5
Tropidin

Conditions

Conditions	Yield
With hydrogenchloride; zinc
With hydrogen iodide; zinc

hydrobromide of α-tropidine hydrobromide: hydrobromide of α-tropidine hydrobromide

A: 529-17-9
tropane

: 529-18-0, 122709-67-5
Tropidin

Conditions

Conditions	Yield
With sulfuric acid; zinc
With hydrogen iodide; zinc

: 3-iodo-tropane

: 7647-01-0
hydrogenchloride

zinc dust: zinc dust

A: 529-17-9
tropane

: 529-18-0, 122709-67-5
Tropidin

...Expand

: 7664-93-9
sulfuric acid

: 532-24-1
tropinone

A: 529-17-9
tropane

B: 120-29-6
3-tropanol

C: 135-97-7
pseudotropine

Conditions

Conditions	Yield
elektrolytische Reduktion an einer Bleikathode;

...Expand

: 532-24-1
tropinone

: 10034-85-2
hydrogen iodide

zinc: zinc

A: 529-17-9
tropane

B: 120-29-6
3-tropanol

C: 135-97-7
pseudotropine

...Expand

: 532-24-1
tropinone

A: 529-17-9
tropane

B tropine, pseudotropine: tropine, pseudotropine

Conditions

Conditions	Yield
elektrolytische Reduktion;
With hydrogen iodide; zinc

: 2292-11-7
3exo-bromo-tropane

: 7664-93-9
sulfuric acid

zinc: zinc

A: 529-17-9
tropane

: 529-18-0, 122709-67-5
Tropidin

...Expand

tropane iodomethylate: tropane iodomethylate

A: 529-17-9
tropane

B: 855405-70-8
cyclohept-3-enyl-dimethyl-amine

Conditions

Conditions	Yield
With silver(l) oxide durch Destillation der entstandenen stark alkal. Loesung der Ammoniumbase;

: 113340-14-0, 146309-07-1
cis-4-[(benzyloxycarbonyl)amino]cyclohept-2-enol

: 529-17-9
tropane

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: 66 percent / LiAlH4 / tetrahydrofuran / 10 h / Heating 2: 90 percent / H2 / 5percent Pd on charcoal / methanol / 16 h 3: 1.) SOCl2, 2.) TABD / 1.) CDCl3, 0 deg C to room temperature, 19.5 h, 2.) 12 h View Scheme

: 146309-04-8
6-Oxa-7-aza-bicyclo[3.2.2]non-8-ene-7-carboxylic acid benzyl ester

: 529-17-9
tropane

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: 67 percent / LiAlH4 / tetrahydrofuran / 10 h / Heating 2: 87 percent / Zn / acetic acid / 4 h / 50 - 60 °C 3: 90 percent / H2 / 5percent Pd on charcoal / methanol / 16 h 4: 1.) SOCl2, 2.) TABD / 1.) CDCl3, 0 deg C to room temperature, 19.5 h, 2.) 12 h View Scheme

: (1S,4R)-4-Methylamino-cyclohept-2-enol

: 529-17-9
tropane

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 90 percent / H2 / 5percent Pd on charcoal / methanol / 16 h 2: 1.) SOCl2, 2.) TABD / 1.) CDCl3, 0 deg C to room temperature, 19.5 h, 2.) 12 h View Scheme

: 214326-04-2
N-methyl-8-oxa-9-azabicyclo[3.2.2]non-6-ene

: 529-17-9
tropane

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: 87 percent / Zn / acetic acid / 4 h / 50 - 60 °C 2: 90 percent / H2 / 5percent Pd on charcoal / methanol / 16 h 3: 1.) SOCl2, 2.) TABD / 1.) CDCl3, 0 deg C to room temperature, 19.5 h, 2.) 12 h View Scheme

: 695-64-7
1-chloro-1-nitrosocyclohexane

: 529-17-9
tropane

Conditions

Conditions	Yield
Multi-step reaction with 6 steps 1: 68 percent / ethanol; CCl4 / 48 h / -10 °C 2: 98 percent / H2 / 5percent Pd/C / methanol / 7 h / 760 Torr 3: 80 percent / Na2CO3 / CHCl3; H2O / 1.) 0 deg C, 30 min, 2.) RT, 2h 4: 12 percent / SOCl2 / CHCl3 / 48 h / Ambient temperature 5: 78 percent / potassium tert-butoxide / benzene; hexamethylphosphoric acid triamide / 2 h / Ambient temperature 6: 72 percent / LiALH4 / tetrahydrofuran / 24 h / Ambient temperature View Scheme
Multi-step reaction with 6 steps 1: 68 percent / ethanol; CCl4 / 48 h / -10 °C 2: 98 percent / H2 / 5percent Pd/C / methanol / 7 h / 760 Torr 3: 80 percent / Na2CO3 / CHCl3; H2O / 1.) 0 deg C, 30 min, 2.) RT, 2h 4: SOCl2, pyridine / diethyl ether / 14 h / Ambient temperature 5: 78 percent / potassium tert-butoxide / benzene; hexamethylphosphoric acid triamide / 2 h / Ambient temperature 6: 72 percent / LiALH4 / tetrahydrofuran / 24 h / Ambient temperature View Scheme
Multi-step reaction with 5 steps 1: 68 percent / ethanol; CCl4 / 48 h / -10 °C 2: 98 percent / H2 / 5percent Pd/C / methanol / 7 h / 760 Torr 3: 80 percent / Na2CO3 / CHCl3; H2O / 1.) 0 deg C, 30 min, 2.) RT, 2h 5: 72 percent / LiALH4 / tetrahydrofuran / 24 h / Ambient temperature View Scheme

: 529-17-9
tropane

: 541-41-3
chloroformic acid ethyl ester

: 6760-98-1
N-(ethoxycarbonyl)nortropane

Conditions

Conditions	Yield
In benzene	95%

: 529-17-9
tropane

: 498-66-8
norborn-2-ene

: C15H25N

Conditions

Conditions	Yield
With scandium tris(ortho-N,N-dimethylaminobenzyl); trityl tetrakis(pentafluorophenyl)borate In toluene at 70℃; for 24h; regiospecific reaction;	90%

: 529-17-9
tropane

: 280-05-7
8-azabicyclo[3.2.1]octane

Conditions

Conditions	Yield
With carbonochloridic acid 1-chloro-ethyl ester In DCE at 0℃; for 4.08333h; Heating / reflux;	83%
With hypochloric acid Reduktion des entstandenen N-Chlor-nortropans;

: 529-17-9
tropane

: 2-(nonafluoro-tert-butoxy)ethyl acrylate

: 6-((1R,5S)-8-azabicyclo[3.2.1]octan-8-yl)-1-((1,1,1,3,3,3-hexafluoro-2-(trifluoromethyl)propan-2-yl)oxy)hexan-3-one

Conditions

Conditions	Yield
With benzophenone; copper diacetate In acetonitrile at 35℃; for 3h; Giese Free Radical Synthesis; Darkness; Inert atmosphere; Irradiation; Sealed tube;	83%

: 529-17-9
tropane

: 78-94-4
methyl vinyl ketone

: 5-((1R,5S)-8-azabicyclo[3.2.1]octan-8-yl)pentan-2-one

Conditions

Conditions	Yield
With benzophenone; copper diacetate In acetonitrile at 35℃; for 16h; Giese Free Radical Synthesis; Darkness; Inert atmosphere; Irradiation; Sealed tube;	73%

: 529-17-9
tropane

: 6760-99-2
8-azabicyclo[3.2.1]octane hydrochloride

Conditions

Conditions	Yield
Stage #1: tropane With chloroformic acid ethyl ester In toluene at 80℃; for 24h; Stage #2: With hydrogenchloride In water at 100℃; for 2h;	72%
Multi-step reaction with 2 steps 1: Et3N / CH2Cl2 2: MeOH View Scheme
Multi-step reaction with 2 steps 1: 95 percent / benzene 2: 90 percent / aq. HCl / Heating View Scheme

: 529-17-9
tropane

: 108-24-7
acetic anhydride

: 769-04-0
8-acetyl-nortropane

Conditions

Conditions	Yield
palladium diacetate at 80℃; for 14h; Neat (no solvent);	70%

: 529-17-9
tropane

: 107-13-1
acrylonitrile

: 4-(8-azabicyclo[3.2.1]octan-8-yl)butanenitrile

Conditions

Conditions	Yield
With benzophenone; copper diacetate In acetonitrile at 35℃; for 5h; Giese Free Radical Synthesis; Darkness; Inert atmosphere; Irradiation; Sealed tube;	69%

: 529-17-9
tropane

: 100-58-3
phenylmagnesium bromide

: 19079-79-9
8-benzyl-8-azabicyclo[3.2.1]octane

Conditions

Conditions	Yield
Stage #1: tropane With 1,4-diaza-bicyclo[2.2.2]octane; tri(4-tolyl)aminium hexafluorophosphate In acetonitrile at -5℃; Inert atmosphere; Stage #2: phenylmagnesium bromide In tetrahydrofuran; acetonitrile at 0℃; for 0.0833333h; Inert atmosphere; regioselective reaction;	66%

: 529-17-9
tropane

: 140-88-5
ethyl acrylate

: ethyl 4-(8-azabicyclo[3.2.1]octan-8-yl)butanoate

Conditions

Conditions	Yield
With benzophenone; copper diacetate In acetonitrile at 35℃; for 3h; Giese Free Radical Synthesis; Darkness; Inert atmosphere; Irradiation; Sealed tube;	61%