CAS No.109-70-6,1-Bromo-3-chloropropane Suppliers

Jinan Finer Chemical Co., Ltd

Product description: Product name 1-Bromo-3-chloropropane CAS number 109-70-6 Assay ≥99% Appearance Colorless transparent liquid Capacity 500mt/year Application Pharmaceutica

1-Bromo-3-chloropropane

Cas:109-70-6

Min.Order:1 Kilogram

FOB Price: $12.0

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Lonwin Chemical Group Limited

1-Bromo-3-chloropropane CAS：109-70-6 Specification Product name 1-Bromo-3-chloropropane CAS number 109-70-6 Assay ≥99% Appearance Colorless transparent liquid Capacity 500mt/year

Factory supply 1-Bromo-3-chloropropane

Cas:109-70-6

Min.Order:1 Kilogram

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Hunan Russell Chemicals Technology Co.,Ltd

high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:any port in China

1-Bromo-3-chloropropane 109-70-6

Cas:109-70-6

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Amadis Chemical Co., Ltd.

1.Professional synthesis laboratory and production base. 2.Strong synthesis team and service team. 3.Professional data management system. 4.We provide the professional test date and product information ,ex. HNMR ,CNMR,FNMR, HPLC/G

Amadis Chemical offer CAS#109-70-6;CAT#A802077

Cas:109-70-6

Min.Order:10 Milligram

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Zouping Sanhao Chemical Co., Ltd .

Name: 1-Bromo-3-chloropropane Synonyms: 1-bromo-3-chloro-propan;3-Bromo-1-chloropropane;3-Chloro-1Chemicalbook-bromopropane;omega-Chlorobromopropane;Propane,1-bromo-3-chloro-;Trimethylenebromidechloride;trimethylenebromidechloride;TRIMETHYLENECHLOROB

1-bromo-3-chloro-propan

Cas:109-70-6

Min.Order:0 Metric Ton

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Pure Chemistry Scientific Inc.

109-70-6 Application:1-Bromo-3-chloropropane

1-Bromo-3-chloropropane

Cas:109-70-6

Min.Order:0

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Synthetic route

: 107-05-1
3-chloroprop-1-ene

: 109-70-6
1,3-chlorobromopropane

Conditions

Conditions	Yield
With hydrogen bromide; dibenzoyl peroxide In benzene at 20℃; for 6h;	92%
With hydrogen bromide
With hydrogen bromide

: 632-02-0
3-chloropropyl p-toluenesulfonate

: 60-29-7
diethyl ether

: ethylmagnesium bromide

A: 543-59-9
1-Chloropentane

B: 109-70-6
1,3-chlorobromopropane

...Expand

: 632-02-0
3-chloropropyl p-toluenesulfonate

: 60-29-7
diethyl ether

: phenylmagnesium bromide

: 109-70-6
1,3-chlorobromopropane

...Expand

: 632-02-0
3-chloropropyl p-toluenesulfonate

: 60-29-7
diethyl ether

: heptyl magnesium (1+); bromide

A: 1002-69-3
decyl chloride

B: 109-70-6
1,3-chlorobromopropane

...Expand

: 106-94-5
propyl bromide

: 109-70-6
1,3-chlorobromopropane

Conditions

Conditions	Yield
With sulfuryl dichloride; dibenzoyl peroxide
With sulfuryl dichloride; dilauryl peroxide
With sulfuryl dichloride; dilauryl peroxide
With sulfuryl dichloride; dibenzoyl peroxide
With chlorine at 25 - 180℃;

: 142-28-9
1,3-Dichloropropane

: 109-70-6
1,3-chlorobromopropane

Conditions

Conditions	Yield
With ethyl bromide; aluminum tri-bromide at 2 - 5℃;

: 142-28-9
1,3-Dichloropropane

A: 109-70-6
1,3-chlorobromopropane

B: 109-64-8
1,3-dibromo-propane

Conditions

Conditions	Yield
With ethyl bromide; aluminum tri-bromide at 2 - 5℃;

: 107-05-1
3-chloroprop-1-ene

A: 3017-95-6, 127054-44-8, 130232-86-9
2-bromo-1-chloropropane

B: 109-70-6
1,3-chlorobromopropane

Conditions

Conditions	Yield
With hydrogen bromide
With hydrogen bromide
With hydrogen bromide

: 627-30-5
1-chloro-3-hydroxypropane

: 109-70-6
1,3-chlorobromopropane

Conditions

Conditions	Yield
With sulfuric acid; hydrogen bromide dann Destillieren;
With phosphorus tribromide
With phosphorus tribromide

: 10035-10-6, 12258-64-9
hydrogen bromide

: 7726-95-6
bromine

: 107-05-1
3-chloroprop-1-ene

: 109-70-6
1,3-chlorobromopropane

Conditions

Conditions	Yield
in Gegenwart von Feuchtigkeit;

...Expand

: 10035-10-6, 12258-64-9
hydrogen bromide

: 107-05-1
3-chloroprop-1-ene

BiCl3: BiCl3

: 109-70-6
1,3-chlorobromopropane

Conditions

Conditions	Yield
in Gegenwart von Feuchtigkeit;

...Expand

: 10035-10-6, 12258-64-9
hydrogen bromide

: 107-05-1
3-chloroprop-1-ene

oxygen: oxygen

: 109-70-6
1,3-chlorobromopropane

Conditions

Conditions	Yield
in Gegenwart von Feuchtigkeit;

...Expand

p-toluenesulfonic acid-<γ-chloro-propyl>-ester: p-toluenesulfonic acid-<γ-chloro-propyl>-ester

alkyl magnesium bromide: alkyl magnesium bromide

: 109-70-6
1,3-chlorobromopropane

Conditions

Conditions	Yield
With diethyl ether

: 7791-25-5
sulfuryl dichloride

: 105-74-8
dilauryl peroxide

: 106-94-5
propyl bromide

A: 3017-96-7
1-bromo-2-chloropropane

B: 109-70-6
1,3-chlorobromopropane

...Expand

: 7791-25-5
sulfuryl dichloride

: 106-94-5
propyl bromide

: 94-36-0
dibenzoyl peroxide

A: 3017-96-7
1-bromo-2-chloropropane

B: 109-70-6
1,3-chlorobromopropane

...Expand

: 10035-10-6, 12258-64-9
hydrogen bromide

: 107-05-1
3-chloroprop-1-ene

A: 3017-95-6, 127054-44-8, 130232-86-9
2-bromo-1-chloropropane

B: 109-70-6
1,3-chlorobromopropane

Conditions

Conditions	Yield
at -18 - 18℃;
unter verschiedenen Bedingungen;
unter verschiedenen Bedingungen;

...Expand

: 10035-10-6, 12258-64-9
hydrogen bromide

: 64-19-7
acetic acid

: 107-05-1
3-chloroprop-1-ene

A: 3017-95-6, 127054-44-8, 130232-86-9
2-bromo-1-chloropropane

B: 109-70-6
1,3-chlorobromopropane

Conditions

Conditions	Yield
at -18 - 18℃;

...Expand

: 74-96-4
ethyl bromide

: 7727-15-3
aluminium bromide

: 142-28-9
1,3-Dichloropropane

A: 109-70-6
1,3-chlorobromopropane

B: 109-64-8
1,3-dibromo-propane

Conditions

Conditions	Yield
at 2 - 5℃;

...Expand

: 107-05-1
3-chloroprop-1-ene

A: 109-70-6
1,3-chlorobromopropane

B CH2ClCHBrCH3: CH2ClCHBrCH3

Conditions

Conditions	Yield
With hydrogen bromide at 100℃;

CH2BrCH2CH2Br: CH2BrCH2CH2Br

A: 109-70-6
1,3-chlorobromopropane

B CH2ClCHBrCH3: CH2ClCHBrCH3

Conditions

Conditions	Yield
With mercury dichloride

: 7647-01-0
hydrogenchloride

: 627-18-9
1-bromo-3-propanol

: 109-70-6
1,3-chlorobromopropane

Conditions

Conditions	Yield
beim Kochen;

: 632-02-0
3-chloropropyl p-toluenesulfonate

: cyclohexyl magnesium (1+); bromide

A: 109-70-6
1,3-chlorobromopropane

B 3-chloro-1-cyclohexyl-propane: 3-chloro-1-cyclohexyl-propane

...Expand

: 632-02-0
3-chloropropyl p-toluenesulfonate

: 60-29-7
diethyl ether

: hexyl magnesium (1+); bromide

A: 109-70-6
1,3-chlorobromopropane

B n-nonyl chloride: n-nonyl chloride

...Expand

: 632-02-0
3-chloropropyl p-toluenesulfonate

: 60-29-7
diethyl ether

: dodecyl magnesium (1+); bromide

A: 109-70-6
1,3-chlorobromopropane

B n-pentadecyl chloride: n-pentadecyl chloride

...Expand

: 108-98-5
thiophenol

: 109-70-6
1,3-chlorobromopropane

: 4911-65-3
3-chloropropyl phenyl sulfide

Conditions

Conditions	Yield
With triethylamine In tetrahydrofuran at 25℃; for 12h;	100%
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 1h;	98%
Stage #1: thiophenol With sodium hydride In tetrahydrofuran; mineral oil at 0℃; for 1h; Inert atmosphere; Stage #2: 1.3-chlorobromopropane In tetrahydrofuran at 0 - 20℃; for 24h; Inert atmosphere;	95%

: 78-82-0
Isobutyronitrile

: 109-70-6
1,3-chlorobromopropane

: 4207-54-9
5-chloro-2,2-dimethylpentanenitrile

Conditions

Conditions	Yield
With lithium hexamethyldisilazane at 70℃; for 16h;	100%
With lithium hexamethyldisilazane at 70℃; for 16h;	100%
With lithium hexamethyldisilazane at 70℃; for 16h;	100%

: 109-70-6
1,3-chlorobromopropane

: 106-45-6
para-thiocresol

: 3147-30-6
γ-chloropropyl 4-methylphenyl sulphide

Conditions

Conditions	Yield
With triethylamine In tetrahydrofuran at 20℃;	100%
With sodium hydroxide In ethanol at 100℃;	65%
With potassium hydroxide

: 1191-99-7
2,3-dihydro-2H-furan

: 109-70-6
1,3-chlorobromopropane

: 110188-06-2
5-(3-chloropropyl)-2,3-dihydrofuran

Conditions

Conditions	Yield
Stage #1: 2,3-dihydro-2H-furan With tert.-butyl lithium In tetrahydrofuran; pentane at -78 - 0℃; for 3h; Inert atmosphere; Stage #2: 1.3-chlorobromopropane In tetrahydrofuran; pentane at -78℃; for 14h; Inert atmosphere;	100%
With N,N,N,N,N,N-hexamethylphosphoric triamide; tert.-butyl lithium 1.) THF, from -78 deg C to 0 deg C, 1.25 h, 2.) THF, from 0 deg C to 25 deg C, 7.33 h; Yield given. Multistep reaction;

: 699-83-2
2,6-dihydroxylacetophenone

: 109-70-6
1,3-chlorobromopropane

: 105277-74-5
2-(3-chlorophenoxy)-6-hydroxyacetophenone

Conditions

Conditions	Yield
With potassium carbonate In acetone for 24h; Heating;	100%
With potassium carbonate In N,N-dimethyl-formamide at 70℃; for 4h;	46%
With potassium carbonate In acetone

: 92-69-3
4-Phenylphenol

: 109-70-6
1,3-chlorobromopropane

: 99472-05-6
4-(3-chloropropoxy)-1,1'-biphenyl

Conditions

Conditions	Yield
With potassium carbonate In acetone for 24h; Williamson Ether Synthesis; Reflux;	100%
With potassium carbonate In acetone for 24h; Heating;	71%
With potassium carbonate In acetone for 24h; Heating;	70%

: 109-70-6
1,3-chlorobromopropane

: 99-93-4
4-Hydroxyacetophenone

: 91427-23-5
1-[4-(3-chloropropoxy)phenyl]ethanone

Conditions

Conditions	Yield
With potassium carbonate In acetone at 65℃; for 18h;	100%
With potassium carbonate In acetone at 65℃;	99%
With potassium carbonate In acetone at 65℃;	99%

: 109-70-6
1,3-chlorobromopropane

: 621-42-1
meta-hydroxyacetanilide

: 78702-97-3
N-<3-(3-chloropropoxy)phenyl>acetamide

Conditions

Conditions	Yield
With potassium carbonate In acetone for 16h; Heating;	100%
With sodium hydroxide In ethanol for 8h; Heating;	65%

: 109-70-6
1,3-chlorobromopropane

: 158220-74-7
N-(3,3-dimethoxy-2-butylidene)isopropylamine

: 163679-86-5
N-(7-chloro-2,2-dimethoxy-3-heptylidene)isopropylamine

Conditions

Conditions	Yield
With lithium diisopropyl amide In tetrahydrofuran; hexane 1.) 0 deg C, 3 h, 2.) rt, 20 h;	100%
Stage #1: N-(3,3-dimethoxy-2-butylidene)isopropylamine With lithium diisopropyl amide In tetrahydrofuran; hexane at 0℃; for 3h; Stage #2: 1.3-chlorobromopropane In tetrahydrofuran; hexane at 0 - 20℃; for 20h;	98%

: 109-70-6
1,3-chlorobromopropane

: 182123-57-5
2-nitro-10H-indolo[3,2-b]quinoline

: 214467-43-3
2-nitro-10-chloropropylindolo[3,2-b]quinoline

Conditions

Conditions	Yield
With sodium hydroxide; dimethyl sulfoxide at 20℃; for 4h; Substitution;	100%

: 51-17-2
benzoimidazole

: 109-70-6
1,3-chlorobromopropane

: 151029-72-0
1-(Benzimidazol-1-yl)-3-chloropropane

Conditions

Conditions	Yield
Stage #1: benzoimidazole With sodium hydride In 1-methyl-pyrrolidin-2-one at 20℃; for 0.5h; Stage #2: 1.3-chlorobromopropane In 1-methyl-pyrrolidin-2-one at 20 - 100℃; for 76h;	100%
With tetrabutylammomium bromide; sodium hydroxide In water at 60℃; for 2.08333h;	62%
With sodium hydride 1) acetonitrile, reflux, 1 h; 2) acetonitrile, reflux, 2 h; Yield given; Multistep reaction;
With potassium carbonate In acetone for 12h; Reflux;

: 40501-41-5
methyl 4'-hydroxy-4-biphenylcarboxylate

: 109-70-6
1,3-chlorobromopropane

: 372514-04-0
Methyl 4'-(3-chloropropoxy)[1,1'-biphenyl]-4-carboxylate

Conditions

Conditions	Yield
With potassium carbonate In butanone for 24h; Heating;	100%
With potassium carbonate In butanone	92%
With potassium carbonate In butanone	92%

: 82380-18-5
2-fluoro-4-hydroxybenzonitrile

: 109-70-6
1,3-chlorobromopropane

: 873547-02-5
4-(3-chloropropoxy)-2-fluorobenzonitrile

Conditions

Conditions	Yield
With potassium carbonate In butanone Heating;	100%

: 109-70-6
1,3-chlorobromopropane

: 133186-55-7
1-(3,5-difluoro-4-hydroxyphenyl)ethanone

: 1005402-88-9
1-[4-(3-chloro-propoxy)-3,5-difluoro-phenyl]-ethanone

Conditions

Conditions	Yield
With potassium carbonate In acetone for 20h; Heating / reflux;	100%

: 1004764-46-8
4-(5-methyl-4, 5,6,7-tetrahydro[1,3]oxazolo[4,5-c]pyridin-2-yl)phenol

: 109-70-6
1,3-chlorobromopropane

: 2-[4-(3-chloropropoxy)phenyl]-5-methyl-4,5,6,7-tetrahydro[1,3]oxazolo[4,5-c]pyridine

Conditions

Conditions	Yield
With potassium carbonate In butanone for 4h; Heating / reflux;	100%

: 1004764-62-8
4-(4-acetyl-5,6,7,8-tetrahydro-4H-[1,3]thiazolo[5,4-b]azepin-2-yl)phenol

: 109-70-6
1,3-chlorobromopropane

: 4-acetyl-2-[4-(3-chloropropoxy)phenyl]-5,6,7,8-tetrahydro-4H-[1,3]thiazolo[5,4-b]azepine

Conditions

Conditions	Yield
With potassium carbonate In butanone for 20h; Heating / reflux;	100%
In ethyl acetate for 20h; Reflux;	100%

: 109-70-6
1,3-chlorobromopropane

: 252061-66-8
5-hydroxy-1,3-dihydro-1-isoindolone

: 928257-25-4
5-(3-chloro-propoxy)-2,3-dihydro-isoindol-1-one

Conditions

Conditions	Yield
With potassium carbonate; potassium iodide In acetonitrile for 18h; Heating / reflux;	100%

: 109-70-6
1,3-chlorobromopropane

: 10387-40-3
potassium thioacetate

: 13012-54-9
thioacetic acid S-(3-chloropropyl) ester

Conditions

Conditions	Yield
In tetrahydrofuran for 1h; Heating;	100%

: 540-38-5
4-Iodophenol

: 109-70-6
1,3-chlorobromopropane

: 273217-89-3
1-(3-chloropropoxy)-4-iodobenzene

Conditions

Conditions	Yield
With potassium carbonate In acetone for 20h; Heating / reflux;	100%
With potassium carbonate In acetone	100%
With potassium carbonate In acetone Heating / reflux;	98%

: 109-70-6
1,3-chlorobromopropane

: 193002-25-4
7-hydroxy-6-methoxy-3-pivaloyloxymethyl-3,4-dihydroquinazolin-4-one

: 264208-49-3
7-(3-chloropropoxy)-6-methoxy-3-((pivaloyloxy)methyl)-3,4-dihydroquinazolin-4-one

Conditions

Conditions	Yield
With potassium carbonate In DMF (N,N-dimethyl-formamide) at 20℃;	100%

: 3-(3-Ethyl-1,2,4-oxadiazol-5-yl)-9H-β-carboline

: 109-70-6
1,3-chlorobromopropane

: 9-(3-Chloro-1-propyl)-3-(3-ethyl-1,2,4-oxadiazol-5-yl)-9H-β-carboline

Conditions

Conditions	Yield
In N,N-dimethyl-formamide; acetone; mineral oil	100%

1,3-Bis(2-methyloropanoyloxy)-propane: 1,3-Bis(2-methyloropanoyloxy)-propane

: propane-1,3-diyl bis(2-methylpropanoate)

: 109-70-6
1,3-chlorobromopropane

: 139483-62-8
1,3-bis(2,2-dimethyl-5-chloropentanoyloxy)-propane

Conditions

Conditions	Yield
With lithium diisopropyl amide In tetrahydrofuran; water	100%

...Expand

: 109-70-6
1,3-chlorobromopropane

: 65145-13-3
2-fluoro-4-hydroxybenzoic acid

: 911135-12-1
3-chloropropyl 4-(3-chloropropoxy)-2-fluorobenzoate

Conditions

Conditions	Yield
With potassium carbonate In butanone at 80℃;	100%

: 2105-94-4
4-bromo-2-fluorophenol

: 109-70-6
1,3-chlorobromopropane

: 181807-91-0
4-bromo-1-(3-chloro-propoxy)-2-fluoro-benzene

Conditions

Conditions	Yield
With potassium carbonate In acetonitrile for 3h; Product distribution / selectivity; Heating / reflux;	100%

: 8-[2-(6,6-dimethyl-bicyclo[3.1.1]hept-2-yl)-ethyl]-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-one

: 109-70-6
1,3-chlorobromopropane

: 3-(3-chloro-propyl)-8-[2-(6,6-dimethyl-bicyclo[3.1.1]hept-2-yl)-ethyl]-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-one

Conditions

Conditions	Yield
Stage #1: 8-[2-(6,6-dimethyl-bicyclo[3.1.1]hept-2-yl)-ethyl]-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-one With potassium tert-butylate In tetrahydrofuran at 0℃; for 0.5h; Stage #2: 1.3-chlorobromopropane In tetrahydrofuran at 0 - 50℃; for 4h;	100%

: 84117-86-2
tert-butyl 1H-indole-2-carboxylate

: 109-70-6
1,3-chlorobromopropane

: 1352949-75-7
tert-butyl 1-(3-chloropropyl)-1H-indole-2-carboxylate

Conditions

Conditions	Yield
Stage #1: tert-butyl 1H-indole-2-carboxylate With sodium hydride In N,N-dimethyl-formamide Stage #2: 1.3-chlorobromopropane In N,N-dimethyl-formamide at 60℃; for 16h;	100%

: 109-70-6
1,3-chlorobromopropane

: 197067-27-9
3,3-difluoro-1,3-dihydro-2H-indol-2-one

: 1352949-54-2
1-(3-chloropropyl)-3,3-difluoroindolin-2-one

Conditions

Conditions	Yield
With sodium hydride In N,N-dimethyl-formamide at 0 - 20℃; for 16h;	100%

: 3,5-difluoro-4-(hydroxymethyl)phenol

: 109-70-6
1,3-chlorobromopropane

: [4-(3-chloropropoxy)-2,6-difluorophenyl]methanol

Conditions

Conditions	Yield
With potassium carbonate In acetonitrile for 3h; Reflux;	100%
With potassium carbonate In acetonitrile for 3h; Reflux;	96%
With potassium carbonate In acetonitrile for 3h; Reflux;	96%

: 149377-19-5
4-(4-hydroxy-phenyl)-piperidine-1-carboxylic acid tert-butyl ester

: 109-70-6
1,3-chlorobromopropane

: tert-butyl 4-(4-(3-chloropropoxy)phenyl)piperidine-1-carboxylate

Conditions

Conditions	Yield
With potassium carbonate In acetonitrile at 80℃; for 16h;	100%
With potassium carbonate In acetone at 90℃; for 40h;

: 98977-34-5
1-tert-butyl 3-ethyl 4-oxopiperidine-1,3-dicarboxylate

: 109-70-6
1,3-chlorobromopropane

: C16H26ClNO5

Conditions

Conditions	Yield
Stage #1: 1-tert-butyl 3-ethyl 4-oxopiperidine-1,3-dicarboxylate With potassium tert-butylate In tetrahydrofuran at -20℃; for 0.5h; Stage #2: 1.3-chlorobromopropane In tetrahydrofuran at 15℃; Inert atmosphere;	100%