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111-25-1

Basic Information
CAS No.: 111-25-1
Name: 1-Bromo hexane
Molecular Structure:
Molecular Structure of 111-25-1 (1-Bromo hexane)
Formula: C6H13Br
Molecular Weight: 165.10
Synonyms: n-Hexyl bromide;1-Hexyl bromide;Bromohexane;Hexyl bromide;NSC 71206;UNII-WVA0FAX7GA;
EINECS: 203-850-2
Density: 1.176 g/cm3
Melting Point: -85 ºC
Boiling Point: 154.9 ºC at 760 mmHg
Flash Point: 57.2 ºC
Solubility: Immiscible with water.
Appearance: colourless liquid
Hazard Symbols: IrritantXi
Risk Codes: 36/37/38-10
Safety: 26-36-16
Transport Information: UN 1993 3/PG 3
PSA: 0.00000
LogP: 2.96160
Synthetic route
544-10-5

1-Chlorohexane

111-25-1

1-bromo-hexane

Conditions
ConditionsYield
With calcium bromide; tetrahexylammonium bromide at 110℃; for 24h;92%
With tetrabutylammomium bromide; lithium chloride In toluene at 70℃; Rate constant; Equilibrium constant; effect of nature of the cation of the salt on the equilibrium constant;
111-27-3

hexan-1-ol

111-25-1

1-bromo-hexane

Conditions
ConditionsYield
With phosphorus tribromide In tetrahydrofuran at 10℃; for 3h; Large scale;91.4%
With phosphorus tribromide for 4h; Cooling with ice;85%
With hydrogen bromide

Pyridine-2-sulfonic acid hexyl ester

A

111-25-1

1-bromo-hexane

B

C5H4NO3S(1-)*Br(1-)*Mg(2+)

Conditions
ConditionsYield
With magnesium bromide ethyl etherate In diethyl ether; dichloromethane at 0℃; for 0.0833333h;A 88%
B n/a
2695-47-8

6-Bromo-1-hexene

111-25-1

1-bromo-hexane

Conditions
ConditionsYield
With hydrogen; 1,5-hexadienerhodium(I)-chloride dimer In hexane for 4h; Ambient temperature; pH=7.6;78%
With hydrogen at 25℃; under 760.051 Torr; for 0.166667h; Catalytic behavior; Reagent/catalyst; Time;
111-27-3

hexan-1-ol

A

6151-90-2

dihexyl phosphonate

B

111-25-1

1-bromo-hexane

Conditions
ConditionsYield
With phosphorus tribromide In diethyl ether at 0 - 25℃; for 6h;A 12.8%
B 75.3%
75-25-2

Bromoform

83498-70-8

2-(hexyloxy)-1,3-dioxolane

A

96-49-1

[1,3]-dioxolan-2-one

B

111-25-1

1-bromo-hexane

C

6065-67-4

formic acid-(2-bromo-ethyl ester)

D

66-25-1

hexanal

E

2-bromoethyl hexyl carbonate

F

74-95-3

1,2-dibromomethane

Conditions
ConditionsYield
dibenzoyl peroxide at 100℃; for 2h; Rate constant; Product distribution; other temperature;A n/a
B n/a
C n/a
D n/a
E 60%
F n/a
75-25-2

Bromoform

2-(hexyloxy)-m-dioxane

A

2453-03-4

trimethylene carbonate

B

111-25-1

1-bromo-hexane

C

53452-10-1

3-Brompropylformiat

D

66-25-1

hexanal

E

3-bromopropyl hexyl carbonate

F

74-95-3

1,2-dibromomethane

Conditions
ConditionsYield
dibenzoyl peroxide at 100℃; for 2h; Rate constant; Product distribution; other temperature;A n/a
B n/a
C n/a
D n/a
E 56%
F n/a
3377-87-5

3-bromohexane

111-25-1

1-bromo-hexane

Conditions
ConditionsYield
50%
112-25-4

2-hexyloxyethanol

A

111-25-1

1-bromo-hexane

B

82175-70-0

(2-bromo-ethyl)-hexyl ether

Conditions
ConditionsYield
With dibromo sulfoxide; urea In 1,2-dichloro-benzene at 30 - 50℃; for 14h; Product distribution / selectivity;A n/a
B 13.5%
592-41-6

1-hexene

111-25-1

1-bromo-hexane

Conditions
ConditionsYield
With hydrogen bromide unter der Einwirkung von stillen elektrischen Entlandungen;
506-96-7

Acetyl bromide

5756-43-4

ethyl n-hexyl ether

A

74-96-4

ethyl bromide

B

111-25-1

1-bromo-hexane

Conditions
ConditionsYield
at 180℃; im Rohr;
110-54-3

hexane

A

111-25-1

1-bromo-hexane

Conditions
ConditionsYield
With bromine Irradiation.bei gleichzeitiger Belichtung mit einer Uviollampe;
With bromine Irradiation.bei gleichzeitiger Belichtung mit einer Uviollampe;
592-41-6

1-hexene

A

111-25-1

1-bromo-hexane

Conditions
ConditionsYield
With borane; bromine; sodium methylate 1.)THF, 0 deg C, 2.) 0 deg C, 3.) MeOH, 0 deg C; Yield given. Multistep reaction;
592-41-6

1-hexene

A

111-25-1

1-bromo-hexane

C

111-27-3

hexan-1-ol

Conditions
ConditionsYield
With borane; bromine In tetrahydrofuran at 20 - 25℃; Product distribution; bromination reaction in presence of various bases; dropwise or simultaneous addition;
110-54-3

hexane

A

3377-87-5

3-bromohexane

B

111-25-1

1-bromo-hexane

Conditions
ConditionsYield
With N-bromo-2,2,6,6-tetramethylpiperidinium perchlorate In trifluoroacetic acid at 5℃; for 8h; Product distribution; Mechanism; Irradiation; different N-bromoammonium perchlorate derivatives;
With N-bromo-2,2,6,6-tetramethylpiperidinium perchlorate In trifluoroacetic acid at 5℃; for 8h; Irradiation; Yield given. Yields of byproduct given;
With bromine; sodium t-butanolate In cyclohexane Heating; Title compound not separated from byproducts;
With N-bromo-N-(t-butyl)-3,5-bis(trifluoromethyl)benzamide In benzene at 20℃; for 4h; Sealed tube; Irradiation; Inert atmosphere; Overall yield = 66.1 %Chromat.;
75-62-7

Bromotrichloromethane

83498-70-8

2-(hexyloxy)-1,3-dioxolane

A

96-49-1

[1,3]-dioxolan-2-one

B

111-25-1

1-bromo-hexane

C

6065-67-4

formic acid-(2-bromo-ethyl ester)

D

66-25-1

hexanal

E

2-bromoethyl hexyl carbonate

F

74-95-3

1,2-dibromomethane

Conditions
ConditionsYield
dibenzoyl peroxide at 90℃; for 2h; Rate constant; Product distribution;
5756-43-4

ethyl n-hexyl ether

111-25-1

1-bromo-hexane

Conditions
ConditionsYield
With trimethylsilyl bromide for 168h; Heating; Yield given;
629-05-0

n-octyne

1116-73-0

trihexylaluminium

A

111-25-1

1-bromo-hexane

B

19780-80-4

6-methylenetridecane

C

41446-63-3

(E)-7-tetradecene

Conditions
ConditionsYield
With copper(I) bromide In hexane 1.) -78 deg C, 2 h, 2.) 20 deg C, 4 h;A 2.0 % Chromat.
B 57.6 % Chromat.
C 5.8 % Chromat.
17888-62-9

hexanoxytrimethylsilane

111-25-1

1-bromo-hexane

Conditions
ConditionsYield
With trimethylsilyl bromide for 168h; Heating; Yield given;
4798-44-1

1-hexene-3-ol

111-25-1

1-bromo-hexane

Conditions
ConditionsYield
With lithium aluminium tetrahydride; bromine; bis(cyclopentadienyl)titanium dichloride 1.) THF; Yield given. Multistep reaction;
4459-32-9

trihexylorthoformate

A

112-40-3

dodecane

B

629-33-4

hexyl formate

C

110-54-3

hexane

D

111-25-1

1-bromo-hexane

E

7523-15-1

di-hexyl carbonate

F

66-25-1

hexanal

Conditions
ConditionsYield
With Perbenzoic acid; Bromoform at 89.9℃; Product distribution; Rate constant; Mechanism; other temperatures: 353 deg K; other peroxide: t-butyl peroxide;
17774-09-3

n-hexyl mercury chloride

111-25-1

1-bromo-hexane

Conditions
ConditionsYield
With Bromotrichloromethane In benzene at 45℃; for 36h; Irradiation;56 % Spectr.
74724-77-9

hexyldiphenylbismutane

A

108-86-1

bromobenzene

B

111-25-1

1-bromo-hexane

Conditions
ConditionsYield
With bromine In dichloromethane -70 deg C to r.t.;A 10 % Chromat.
B 62 % Chromat.
162104-75-8

hexyl 3-methylcyclohexa-1,4-diene-3-carboxylate

A

111-25-1

1-bromo-hexane

B

6789-88-4

hexyl benzoate

C

108-88-3

toluene

Conditions
ConditionsYield
With N-Bromosuccinimide; (PhCO2)2O In tetrachloromethane for 16h; Product distribution; Heating; other cyclohexa-1,4-diene-3-carboxylates, 2,5-dihydrofuran-2-carboxylates;A 3 % Chromat.
B 2 % Chromat.
C 7 % Chromat.
With N-Bromosuccinimide; dilauryl peroxide In tetrachloromethane for 5h; Mechanism; Product distribution;A 7 % Chromat.
B 4 % Chromat.
C 3 % Chromat.
7664-93-9

sulfuric acid

111-27-3

hexan-1-ol

sodium bromide

sodium bromide

A

111-25-1

1-bromo-hexane

enanthate thallium

enanthate thallium

111-25-1

1-bromo-hexane

Conditions
ConditionsYield
With tetrachloromethane; bromine
With tetrachloromethane; bromine
110-54-3

hexane

7726-95-6

bromine

A

3377-87-5

3-bromohexane

B

111-25-1

1-bromo-hexane

Conditions
ConditionsYield
im Sonnenlichte bei Siedetemperatur;
111-25-1

1-bromo-hexane

90-02-8

salicylaldehyde

7162-59-6

2-hexyloxybenzaldehyde

Conditions
ConditionsYield
With potassium hydroxide; potassium iodide In ethanol for 32h; Heating;100%
With potassium carbonate In N,N-dimethyl-formamide at 130℃; for 20h;99%
Stage #1: salicylaldehyde With sodium carbonate In N,N-dimethyl-formamide at 20℃; for 0.5h;
Stage #2: 1-bromo-hexane In N,N-dimethyl-formamide at 20℃; for 24h;
75.3%
111-25-1

1-bromo-hexane

108-98-5

thiophenol

943-78-2

hexyl phenyl sulfide

Conditions
ConditionsYield
With potassium carbonate In dimethyl sulfoxide at 20 - 50℃; for 2.16667h; Inert atmosphere;100%
With ethanol; sodium ethanolate
With potassium hydroxide
cetyltributylphosphonium bromide
With potassium carbonate In N,N-dimethyl-formamide at 85℃; for 12h;
111-25-1

1-bromo-hexane

603-35-0

triphenylphosphine

4762-26-9

hexyltriphenylphosphonium bromide

Conditions
ConditionsYield
In toluene for 8h; Reflux;100%
In acetonitrile for 16h; Heating;95.6%
In toluene for 120h; Heating;92%
101132-13-2

2-morpholino-3-pentenenitrile

111-25-1

1-bromo-hexane

84104-04-1

2-hexyl-2-morpholino-3-pentenenitrile

Conditions
ConditionsYield
With lithium diisopropyl amide In tetrahydrofuran100%
111-25-1

1-bromo-hexane

95-71-6

2-methylbenzene-1,4-diol

157202-49-8

1,4-Dihexyloxy-2-methylbenzol

Conditions
ConditionsYield
With potassium hydroxide; Aliquat 336 In 1,2-dimethoxyethane for 24h; Heating;100%
In ethanol Etherification; Heating;
111-25-1

1-bromo-hexane

6089-04-9

3-(tetrahydropyran-2'-yloxy)propyne

83583-29-3

non-2-ynyl tetrahydropyran-2-yl ether

Conditions
ConditionsYield
Stage #1: 3-(tetrahydropyran-2'-yloxy)propyne With n-butyllithium In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide at -78℃;
Stage #2: 1-bromo-hexane In tetrahydrofuran
100%
With sodium amide
With n-butyllithium In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; hexane Ambient temperature;
With ammonium chloride; lithium; iron(III) chloride In ammonia
111-25-1

1-bromo-hexane

123-08-0

4-hydroxy-benzaldehyde

5736-94-7

4-(hexyloxy)benzaldehyde

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 20h; Williamson ether synthesis;100%
Stage #1: 4-hydroxy-benzaldehyde With potassium carbonate In N,N-dimethyl-formamide at 60℃; for 1h;
Stage #2: 1-bromo-hexane In N,N-dimethyl-formamide at 80℃; Inert atmosphere;
99%
With potassium carbonate In acetonitrile Reflux;96%
111-25-1

1-bromo-hexane

767-00-0

4-cyanophenol

66052-06-0

1-(4-cyanophenyl)oxyhexane

Conditions
ConditionsYield
In potassium carbonate100%
With sodium hydride In N,N-dimethyl-formamide 1.) rt, 1 h, 2.) reflux, 12 h;90%
With potassium carbonate In cyclohexanone for 24h; Heating;70%
111-25-1

1-bromo-hexane

ethyl (S)-6-hydroxy-2-methylchroman-2-carboxylate

(S)-6-Hexyloxy-2-methyl-chroman-2-carboxylic acid ethyl ester

Conditions
ConditionsYield
With sodium hydride; potassium iodide In N,N-dimethyl-formamide at 80℃; for 48h; Etherification;100%
1142-19-4

4,4'-dichlorodiphenyl disulfide

111-25-1

1-bromo-hexane

59693-91-3

n-Hexyl-p-chlorphenylsulfid

Conditions
ConditionsYield
Stage #1: 4,4'-dichlorodiphenyl disulfide With aluminium trichloride; zinc In water; N,N-dimethyl-formamide at 65℃; S-S bond cleavage;
Stage #2: 1-bromo-hexane In water; N,N-dimethyl-formamide at 65℃; for 18h; Substitution;
100%
With aluminium trichloride; zinc In water; N,N-dimethyl-formamide at 65℃; for 18h;100 % Chromat.
616-47-7

1-methyl-1H-imidazole

111-25-1

1-bromo-hexane

85100-78-3

1-hexyl-3-methyl-1-imidazolium bromide

Conditions
ConditionsYield
at 140℃; Continuous flow; neat (no solvent);100%
In dichloromethane at 20℃; for 0.25h; Cooling with ice;99.87%
In toluene at 65℃; for 5h;98%
86-73-7

9H-fluorene

111-25-1

1-bromo-hexane

123863-97-8

9,9-dihexyl-9H-fluorene

Conditions
ConditionsYield
Stage #1: 9H-fluorene With n-butyllithium In tetrahydrofuran at -78℃;
Stage #2: 1-bromo-hexane In tetrahydrofuran at -78 - 20℃; for 12h; Further stages.;
100%
With tetra-(n-butyl)ammonium iodide; sodium hydroxide100%
Stage #1: 9H-fluorene With n-butyllithium In tetrahydrofuran at -78℃; for 0.75h;
Stage #2: 1-bromo-hexane In tetrahydrofuran at -78 - 20℃; for 3h;
99%
111-25-1

1-bromo-hexane

1133-80-8

2-bromo-9H-fluorene

226070-05-9

2-bromo-9,9-dihexyl-9H-fluorene

Conditions
ConditionsYield
With sodium hydroxide; N-benzyl-N,N,N-triethylammonium chloride In dimethyl sulfoxide100%
Stage #1: 2-bromo-9H-fluorene With potassium tert-butylate In N,N-dimethyl-formamide at 20℃; for 0.25h; Inert atmosphere;
Stage #2: 1-bromo-hexane In N,N-dimethyl-formamide at 60℃; Inert atmosphere;
100%
Stage #1: 2-bromo-9H-fluorene With potassium iodide; potassium hydroxide In dimethyl sulfoxide for 0.333333h; Heating; Inert atmosphere;
Stage #2: 1-bromo-hexane In dimethyl sulfoxide at 20℃; for 3.6h; Inert atmosphere;
100%
111-25-1

1-bromo-hexane

548-35-6

truxene

600172-85-8

5,5,10,10,15,15-hexahexyltruxene

Conditions
ConditionsYield
Stage #1: truxene With n-butyllithium In tetrahydrofuran at -78℃; for 2h;
Stage #2: 1-bromo-hexane In tetrahydrofuran at -78 - 20℃;
100%
Stage #1: truxene With n-butyllithium In tetrahydrofuran at -78℃; for 2h; Inert atmosphere;
Stage #2: 1-bromo-hexane In tetrahydrofuran at 20℃; Inert atmosphere;
95%
Stage #1: truxene With n-butyllithium In tetrahydrofuran; hexane at -78 - 20℃; for 2.5h; Inert atmosphere;
Stage #2: 1-bromo-hexane In tetrahydrofuran; hexane at -78 - 20℃; for 12h;
95%
111-25-1

1-bromo-hexane

444-30-4

2-(trifluoromethyl)phenol

872123-27-8

1-(hexyloxy)-2-(trifluoromethyl)benzene

Conditions
ConditionsYield
With potassium tert-butylate In N,N-dimethyl-formamide at 20℃; for 2.5h;100%
With potassium carbonate In various solvent(s) Heating;75%
1072-63-5

1-vinylimidazole

111-25-1

1-bromo-hexane

1-vinyl-3-hexyl-1H-imidazol-3-ium bromide

Conditions
ConditionsYield
at 110℃; Continuous flow; neat (no solvent);100%
Microwave irradiation;82.6%
In tetrahydrofuran at 60℃; for 48h;51.63%
1008131-36-9

C76H21N3O2

111-25-1

1-bromo-hexane

1008131-37-0

Br(1-)*C82H34N3O2(1+)

Conditions
ConditionsYield
at 100℃; for 48h;100%
1008131-33-6

C72H21N3

111-25-1

1-bromo-hexane

1008131-34-7

Br(1-)*C78H34N3(1+)

Conditions
ConditionsYield
at 100℃; for 48h;100%
443-69-6

5-fluoro-1H-indole-2,3-dione

111-25-1

1-bromo-hexane

85511-62-2

5-fluoro-1-hexyl-isatin

Conditions
ConditionsYield
With caesium carbonate In N,N-dimethyl-formamide at 140℃; Microwave irradiation;100%
111-25-1

1-bromo-hexane

17630-76-1

5-chloroindole 2,3-dione

79183-52-1

5-chloro-1-hexyl-isatin

Conditions
ConditionsYield
With caesium carbonate In N,N-dimethyl-formamide at 140℃; Microwave irradiation;100%
111-25-1

1-bromo-hexane

3470-50-6

6-Hydroxy-1-tetralone

62324-94-1

6-(hexyloxy)-3,4-dihydronaphthalen-1(2H)-one

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 85℃;100%
111-25-1

1-bromo-hexane

62-23-7

4-nitro-benzoic acid

6268-24-2

4-nitrophenyl hexanoate

Conditions
ConditionsYield
With potassium carbonate In acetone for 48h; Reflux;100%
111-25-1

1-bromo-hexane

269409-70-3

4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol

921937-76-0

2-(4-(hexyloxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Conditions
ConditionsYield
With potassium carbonate at 120℃; for 11h; Inert atmosphere;100%
With potassium carbonate In acetone Reflux;64%
With tetra-(n-butyl)ammonium iodide; potassium carbonate In tetrahydrofuran for 3h; Reflux;
111-25-1

1-bromo-hexane

1355089-63-2

tert-butyl 3-{7-fluoro-6-hydroxy-2H-spiro[1-benzofuran-3,4'-piperidine]-1'-yl}propanoate

1355089-67-6

tert-butyl 3-{7-fluoro-6-(hexyloxy)-2H-spiro[1-benzofuran-3,4'-piperidine]-1'-yl}propanoate

Conditions
ConditionsYield
Stage #1: 1-bromo-hexane; tert-butyl 3-{7-fluoro-6-hydroxy-2H-spiro[1-benzofuran-3,4'-piperidine]-1'-yl}propanoate With potassium carbonate In acetonitrile at 75℃;
Stage #2: In acetonitrile
100%
111-25-1

1-bromo-hexane

28177-48-2

2,6-difluorophenol

1562104-17-9

2,4-difluoro-3-hexyloxybenzene

Conditions
ConditionsYield
With potassium tert-butylate In N,N-dimethyl-formamide at 80℃; for 4h;100%
With potassium carbonate In acetonitrile for 24h; Reflux;84%
1072-97-5

5-bromo-2-pyridylamine

111-25-1

1-bromo-hexane

5-bromo-N,N-dihexylpyridin-2-amine

Conditions
ConditionsYield
With sodium hydride In tetrahydrofuran at 50℃;100%
With sodium hydride In tetrahydrofuran at 50℃; Reflux;
111-25-1

1-bromo-hexane

87-48-9

5-Bromo-1H-indole-2,3-dione

C14H16BrNO2

Conditions
ConditionsYield
With sodium hydride In N,N-dimethyl-formamide at 110℃; for 16h;100%
271-63-6

7-Azaindole

111-25-1

1-bromo-hexane

418795-22-9

C13H18N2

Conditions
ConditionsYield
With sodium hydride In N,N-dimethyl-formamide at 20℃;100%
111-25-1

1-bromo-hexane

113798-74-6

2,3,6-trifluorophenol

C12H15F3O

Conditions
ConditionsYield
With potassium tert-butylate In N,N-dimethyl-formamide at 20℃;100%
111-25-1

1-bromo-hexane

(E)-N'-(1H-imidazol-2-yl)-N,N-dimethylformimidamide

(E)-N'-(1-hexyl-1H-imidazol-2-yl)-N,N-dimethylformimidamide

Conditions
ConditionsYield
With potassium tert-butylate In N,N-dimethyl-formamide at 40℃;100%
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    111-25-1

    n-Hexyl bromide

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  • 1- Bromo hexane

  • Casno:

    111-25-1

    1- Bromo hexane

    Min.Order: 1 Kilogram

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  • 1-Bromohexane

  • Casno:

    111-25-1

    1-Bromohexane

    Min.Order: 100 Gram

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  • Bromohexane

  • Casno:

    111-25-1

    Bromohexane

    Min.Order: 0

    FOB Price:  USD $ 0.0-0.0/

    Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS

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    Tel:+86-592 599 8717

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Specification

The 1-Bromo hexane, with the CAS registry number 111-25-1, is also known as n-Hexyl bromide. It belongs to the product categories of Industrial/Fine Chemicals; Intermediates; Alkyl Bromide; Bromine Compounds; Alkyl Bromides; Monofunctional & alpha,omega-Bifunctional Alkanes; Monofunctional Alkanes. Its EINECS registry number is 203-850-2. This chemical's molecular formula is C6H13Br and molecular weight is 165.07. What's more, its IUPAC name is the same with its product name. It is a liquid organohalide and its refractive index is 1.4478 (20 °C, D). This chemical can be prepared by Bromine with Heptanoic acid and this reaction needs reagent perchloromethane. It should be kept in a cold and dry place.

Physical properties about 1-Bromo hexane are: (1)ACD/LogP: 3.81; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 3.8; (4)ACD/LogD (pH 7.4): 3.8; (5)ACD/BCF (pH 5.5): 458.84; (6)ACD/BCF (pH 7.4): 458.84; (7)ACD/KOC (pH 5.5): 2797.84; (8)ACD/KOC (pH 7.4): 2797.84; (9)#H bond acceptors: 0; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 4; (12)Polar Surface Area: 0 Å2; (13)Index of Refraction: 1.446; (14)Molar Refractivity: 37.57 cm3; (15)Molar Volume: 140.7 cm3; (16)Surface Tension: 27.7 dyne/cm; (17)Density: 1.172 g/cm3; (18)Flash Point: 57.2 °C; (19) Enthalpy of Vaporization: 37.55 kJ/mol ; (20)Boiling Point: 154.9 °C at 760 mmHg; (21) Vapour Pressure: 4 mmHg at 25 °C.

Uses of 1-Bromo hexane: (1) it is used as solvents and organic synthesis intermediates; (2) it is used to manufacture pharmaceuticals and organic. For example, it can react with Piperidine to get 1-Hexyl-piperidine. The reaction occurs with reagent potassium carbonate, solvent butan-2-one and other condition of heating for 7 hours. The yield is 83 %.

1-Bromohexane can react with Piperidine to get 1-Hexyl-piperidine.

When you are dealing with this chemical, you should be very careful. This chemical is inflammation to the skin, eyes and respiratory system or other mucous membranes. What's more, it's flammable. Therefore, you should wear suitable protective clothing. And in case of contacting with eyes, you should rinse immediately with plenty of water and seek medical advice.

You can still convert the following datas into molecular structure:
(1) SMILES: BrCCCCCC
(2) InChI: InChI=1S/C6H13Br/c1-2-3-4-5-6-7/h2-6H2,1H3
(3) InChIKey: MNDIARAMWBIKFW-UHFFFAOYSA-N

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mammal (species unspecified) LC50 inhalation 13600mg/m3 (13600mg/m3)   Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 18(4), Pg. 55, 1974.
mouse LD50 intraperitoneal 1226mg/kg (1226mg/kg)   Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 20(12), Pg. 52, 1976.
rat LC50 inhalation 550gm/m3/30M (550000mg/m3)   Fiziologicheski Aktivnye Veshchestva. Physiologically Active Substances. Vol. 7, Pg. 35, 1975.