Product Name

  • Name

    HEXYL CHLOROFORMATE

  • EINECS 228-036-4
  • CAS No. 6092-54-2
  • Article Data16
  • CAS DataBase
  • Density 1.035g/cm3
  • Solubility
  • Melting Point
  • Formula C7H13ClO2
  • Boiling Point 187.2 °C at 760 mmHg
  • Molecular Weight 164.632
  • Flash Point 56.3 °C
  • Transport Information
  • Appearance Clear colorless liquid
  • Safety 26-27-36/37/39-45
  • Risk Codes 23/24/25-34
  • Molecular Structure Molecular Structure of 6092-54-2 (HEXYL CHLOROFORMATE)
  • Hazard Symbols ToxicT
  • Synonyms Formicacid, chloro-, hexyl ester (7CI,8CI);Hexyl alcohol, chloroformate (6CI);Chloroformic acid n-hexyl ester;Hexyl chlorocarbonate;Hexyl chloroformate;Hexyloxycarbonyl chloride;n-Hexyl chloroformate;
  • PSA 26.30000
  • LogP 2.94210

Synthetic route

bis(trichloromethyl) carbonate
32315-10-9

bis(trichloromethyl) carbonate

hexan-1-ol
111-27-3

hexan-1-ol

n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

Conditions
ConditionsYield
Stage #1: bis(trichloromethyl) carbonate With potassium carbonate; N,N-dimethyl-formamide In toluene at 0℃; for 0.5h; Inert atmosphere;
Stage #2: hexan-1-ol In toluene at 0 - 20℃; for 12h; Inert atmosphere;		83%
With pyridine In dichloromethane for 0.166667h;
With triethylamine In dichloromethane cooling;
With pyridine In dichloromethane at 0 - 20℃; for 2h;
With triethylamine In dichloromethane at 0 - 10℃; for 2h;
phosgene
75-44-5

phosgene

hexan-1-ol
111-27-3

hexan-1-ol

n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

hexan-1-ol
111-27-3

hexan-1-ol

trichloromethyl chloroformate
503-38-8

trichloromethyl chloroformate

n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

Conditions
ConditionsYield
With pyrographite In tetrahydrofuran at 20℃; for 1h; Condensation;
With dmap In toluene at 20℃; for 24h;
chloroform
67-66-3

chloroform

hexan-1-ol
111-27-3

hexan-1-ol

n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

Conditions
ConditionsYield
With oxygen at 30℃; for 3h; Irradiation;
n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

(R)-Phenylglycinol
56613-80-0

(R)-Phenylglycinol

hexyl (1R)-2-hydroxy-1-phenylethylcarbamate
532986-19-9

hexyl (1R)-2-hydroxy-1-phenylethylcarbamate

Conditions
ConditionsYield
With sodium hydrogencarbonate In 1,4-dioxane at 0℃; for 2h;99%
n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

4,6-O-benzylidene-1-O-methyl-α-D-glucopyranoside
3162-96-7

4,6-O-benzylidene-1-O-methyl-α-D-glucopyranoside

C28H42O10

C28H42O10

Conditions
ConditionsYield
With N,N,N,N,-tetramethylethylenediamine In dichloromethane at 0℃; for 1h;99%
1-methyl-2-[N-(4-amidino-phenyl)-aminomethyl]-benzimidazol-5-yl-carboxylic acid N-(2-pyridyl)-N-2-(ethoxycarbonylethyl)-amide p-toluenesulfonic acid salt
872728-85-3

1-methyl-2-[N-(4-amidino-phenyl)-aminomethyl]-benzimidazol-5-yl-carboxylic acid N-(2-pyridyl)-N-2-(ethoxycarbonylethyl)-amide p-toluenesulfonic acid salt

n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

dabigatran etexilate
211915-06-9

dabigatran etexilate

Conditions
ConditionsYield
With potassium carbonate In acetonitrile at 0℃; Reagent/catalyst; Solvent; Temperature;98.4%
With potassium carbonate In water; acetone at 12 - 25℃; for 1.5h; Solvent; Temperature; Time;17.5 g
n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

benzylamine
100-46-9

benzylamine

hexyl benzylcarbamate
1239969-89-1

hexyl benzylcarbamate

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0℃; Inert atmosphere;98%
n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

4-aminobenzamidine dihydrochloride
2498-50-2

4-aminobenzamidine dihydrochloride

4-aminobenzamidine-N-hexylcarbamate hydrochloride
1307233-93-7

4-aminobenzamidine-N-hexylcarbamate hydrochloride

Conditions
ConditionsYield
Stage #1: n-hexyl chloroformate; 4-aminobenzamidine dihydrochloride With sodium hydroxide In acetone at 5 - 20℃; for 0.25h;
Stage #2: With hydrogenchloride In water		97.2%
n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

4-nitrobenzamidine
25412-75-3

4-nitrobenzamidine

p-nitrobenzamidine iminocarboxylate

p-nitrobenzamidine iminocarboxylate

Conditions
ConditionsYield
With potassium carbonate In ethyl acetate at 0℃; for 1.5h; Temperature; Time; Reagent/catalyst;96.7%
n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

(1R,2S)-1-amino-1-(3-methoxyphenyl)propan-2-ol hydrochloride

(1R,2S)-1-amino-1-(3-methoxyphenyl)propan-2-ol hydrochloride

hexyl (1R,2S)-2-hydroxy-1-(3-methoxyphenyl)propylcarbamate
289051-64-5

hexyl (1R,2S)-2-hydroxy-1-(3-methoxyphenyl)propylcarbamate

Conditions
ConditionsYield
With sodium hydrogencarbonate In tetrahydrofuran; water at 0 - 20℃; for 1h;96%
n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

phenethylamine
64-04-0

phenethylamine

hexyl phenethylcarbamate

hexyl phenethylcarbamate

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0℃; Inert atmosphere;96%
n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

5-[(tert-butyldimethylsilyl)oxy]pyridin-2-amine

5-[(tert-butyldimethylsilyl)oxy]pyridin-2-amine

hexyl N-[5-[(tert-butyldimethylsilyl)oxy]pyridin-2-yl]carbamate

hexyl N-[5-[(tert-butyldimethylsilyl)oxy]pyridin-2-yl]carbamate

Conditions
ConditionsYield
With pyridine for 2h;95%
1-methyl-2-[N-[4-(1,2,4-oxadiazol-5-one-3-yl)phenyl]-amino-methyl]-benzimidazol-5-yl-carboxylic acid N-(2-pyridyl)-N-(2-ethoxycarbonylethyl)amide
872728-84-2

1-methyl-2-[N-[4-(1,2,4-oxadiazol-5-one-3-yl)phenyl]-amino-methyl]-benzimidazol-5-yl-carboxylic acid N-(2-pyridyl)-N-(2-ethoxycarbonylethyl)amide

n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

ethyl 3-(1-{2-[({4-[amino({[(hexyloxy)carbonyl]imino})methyl]phenyl}amino)methyl]-1-methyl-1H-1,3-benzodiazol-5-yl}-N-(pyridin-2-yl)formamido)propanoate
211915-06-9

ethyl 3-(1-{2-[({4-[amino({[(hexyloxy)carbonyl]imino})methyl]phenyl}amino)methyl]-1-methyl-1H-1,3-benzodiazol-5-yl}-N-(pyridin-2-yl)formamido)propanoate

Conditions
ConditionsYield
Stage #1: 1-methyl-2-[N-[4-(1,2,4-oxadiazol-5-one-3-yl)phenyl]-amino-methyl]-benzimidazol-5-yl-carboxylic acid N-(2-pyridyl)-N-(2-ethoxycarbonylethyl)amide With hydrogen; palladium 10% on activated carbon In tetrahydrofuran; water at 40℃; under 3000.3 Torr; for 0.416667h;
Stage #2: n-hexyl chloroformate With potassium carbonate In tetrahydrofuran; water at 20 - 45℃; Product distribution / selectivity;		94%
n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

6-Chloro-2-methyl-4-(4-methylsulfanyl-phenyl)-1,4-dihydro-pyrimidine-5-carboxylic acid ethyl ester
97934-95-7

6-Chloro-2-methyl-4-(4-methylsulfanyl-phenyl)-1,4-dihydro-pyrimidine-5-carboxylic acid ethyl ester

4-Chloro-2-methyl-6-(4-methylsulfanyl-phenyl)-3,6-dihydro-1λ5-pyrimidine-1,5-dicarboxylic acid 5-ethyl ester 1-hexyl ester

4-Chloro-2-methyl-6-(4-methylsulfanyl-phenyl)-3,6-dihydro-1λ5-pyrimidine-1,5-dicarboxylic acid 5-ethyl ester 1-hexyl ester

Conditions
ConditionsYield
With sodium hydride In tetrahydrofuran at 80℃; for 2h;93%
n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

benzyl (2S,3R)-3-[(2-aminopyridin-4-yl)methyl]-4-oxo-1-{[(1R)-1-phenylethyl]carbamoyl}azetidine-2-carboxylate

benzyl (2S,3R)-3-[(2-aminopyridin-4-yl)methyl]-4-oxo-1-{[(1R)-1-phenylethyl]carbamoyl}azetidine-2-carboxylate

benzyl (2S,3R)-3-[(2-{[(hexyloxy)carbonyl]amino}pyridin-4-yl)methyl]-4-oxo-1-{[(1R)-1-phenylethyl]carbamoyl}azetidine-2-carboxylate

benzyl (2S,3R)-3-[(2-{[(hexyloxy)carbonyl]amino}pyridin-4-yl)methyl]-4-oxo-1-{[(1R)-1-phenylethyl]carbamoyl}azetidine-2-carboxylate

Conditions
ConditionsYield
With pyridine In dichloromethane at 0 - 25℃; for 3.5h; Inert atmosphere;92%
n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

4-bromobenzamidine
22265-36-7

4-bromobenzamidine

C14H19BrN2O2

C14H19BrN2O2

Conditions
ConditionsYield
Stage #1: 4-bromobenzamidine With potassium carbonate In tetrahydrofuran; water at 20℃; for 0.25h;
Stage #2: n-hexyl chloroformate In tetrahydrofuran; water for 12h;		90.4%
n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

1-benzyl-N-[(4-carbamimidoylphenyl)methyl]pyrazole-4-carboxamide hydrochloride

1-benzyl-N-[(4-carbamimidoylphenyl)methyl]pyrazole-4-carboxamide hydrochloride

(Z)-hexyl amino-(4-((1-benzylpyrazole-4-carbonylamino)methyl)phenyl)methylenecarbamate
1312689-18-1

(Z)-hexyl amino-(4-((1-benzylpyrazole-4-carbonylamino)methyl)phenyl)methylenecarbamate

Conditions
ConditionsYield
With potassium carbonate In tetrahydrofuran; water at 20℃; for 1h;90%
n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

N-[(4-carbamimidoylphenyl)methyl]-1-(4-fluorophenyl)-2,5-dimethyl-pyrrole-3-carboxamide hydrochloride

N-[(4-carbamimidoylphenyl)methyl]-1-(4-fluorophenyl)-2,5-dimethyl-pyrrole-3-carboxamide hydrochloride

(Z)-hexyl amino-(4-((1-(4-fluorophenyl)-2,5-dimethyl-pyrrole-3-carbonylamino)methyl)phenyl)methylenecarbamate
1312689-19-2

(Z)-hexyl amino-(4-((1-(4-fluorophenyl)-2,5-dimethyl-pyrrole-3-carbonylamino)methyl)phenyl)methylenecarbamate

Conditions
ConditionsYield
With potassium carbonate In tetrahydrofuran; water at 20℃; for 1h;90%
n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

p-chlorobenzamidine
19563-04-3

p-chlorobenzamidine

C14H19ClN2O2

C14H19ClN2O2

Conditions
ConditionsYield
Stage #1: p-chlorobenzamidine With triethylamine In tetrahydrofuran; water at 20℃; for 0.25h;
Stage #2: n-hexyl chloroformate In tetrahydrofuran; water for 12h;		89.6%
methanesulfonic acid
75-75-2

methanesulfonic acid

1-methyl-2-[N-(4-amidino-phenyl)-aminomethyl]-benzimidazol-5-yl-carboxylic acid N-(2-pyridyl)-N-2-(ethoxycarbonylethyl)-amide p-toluenesulfonic acid salt
872728-85-3

1-methyl-2-[N-(4-amidino-phenyl)-aminomethyl]-benzimidazol-5-yl-carboxylic acid N-(2-pyridyl)-N-2-(ethoxycarbonylethyl)-amide p-toluenesulfonic acid salt

n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

[14C]-Dabigatran etexilate mesylate

[14C]-Dabigatran etexilate mesylate

Conditions
ConditionsYield
Stage #1: 1-methyl-2-[N-(4-amidino-phenyl)-aminomethyl]-benzimidazol-5-yl-carboxylic acid N-(2-pyridyl)-N-2-(ethoxycarbonylethyl)-amide p-toluenesulfonic acid salt; n-hexyl chloroformate With potassium carbonate In water; acetone at 20 - 50℃;
Stage #2: methanesulfonic acid In acetone at 30 - 36℃; for 0.333333h; Product distribution / selectivity;		89%
Stage #1: 1-methyl-2-[N-(4-amidino-phenyl)-aminomethyl]-benzimidazol-5-yl-carboxylic acid N-(2-pyridyl)-N-2-(ethoxycarbonylethyl)-amide p-toluenesulfonic acid salt; n-hexyl chloroformate With potassium carbonate In methanol at 20℃; for 3h;
Stage #2: methanesulfonic acid In water; acetone at 42℃;
...Expand
n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

1-methyl-2-[N-(4-amidinophenyl)-aminomethyl]benzimidazol-5-yl-carboxylicacid-N-(2-pyridyl)-N-(2-ethoxycarbonylethyl)-amide hydrochloride

1-methyl-2-[N-(4-amidinophenyl)-aminomethyl]benzimidazol-5-yl-carboxylicacid-N-(2-pyridyl)-N-(2-ethoxycarbonylethyl)-amide hydrochloride

dabigatran etexilate
211915-06-9

dabigatran etexilate

Conditions
ConditionsYield
With triethylamine In acetone at 0 - 20℃; for 1.5h; Product distribution / selectivity; Inert atmosphere;89%
Stage #1: 1-methyl-2-[N-(4-amidinophenyl)-aminomethyl]benzimidazol-5-yl-carboxylicacid-N-(2-pyridyl)-N-(2-ethoxycarbonylethyl)-amide hydrochloride With hydrogenchloride In 2-methyltetrahydrofuran; water at 25℃; pH=3.5;
Stage #2: With potassium carbonate In 2-methyltetrahydrofuran; water at 25℃; for 0.5h;
Stage #3: n-hexyl chloroformate In 2-methyltetrahydrofuran; water at 25℃; for 2h;		83%
n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

3-Phenylpropan-1-amine
2038-57-5

3-Phenylpropan-1-amine

hexyl (3-phenylpropyl)carbamate

hexyl (3-phenylpropyl)carbamate

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0℃; Inert atmosphere;89%
n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

4-phenyl-1-butylamine
13214-66-9

4-phenyl-1-butylamine

hexyl (4-phenylbutyl)carbamate

hexyl (4-phenylbutyl)carbamate

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0℃; Inert atmosphere;89%
n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

4-(methoxycarbonyloxy)benzhydrol

4-(methoxycarbonyloxy)benzhydrol

n-hexyl 4-(methoxycarbonyloxy)benzhydryl carbonate

n-hexyl 4-(methoxycarbonyloxy)benzhydryl carbonate

Conditions
ConditionsYield
With pyridine at 0℃; for 1h;89%
1-methyl-2-[N-(4-amidino-phenyl)-aminomethyl]-benzimidazol-5-yl-carboxylic acid N-(2-pyridyl)-N-2-(ethoxycarbonylethyl)-amide p-toluenesulfonic acid salt
872728-85-3

1-methyl-2-[N-(4-amidino-phenyl)-aminomethyl]-benzimidazol-5-yl-carboxylic acid N-(2-pyridyl)-N-2-(ethoxycarbonylethyl)-amide p-toluenesulfonic acid salt

n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

dabigatran etexilate
211915-06-9

dabigatran etexilate

Conditions
ConditionsYield
With triethylamine In dichloromethane at 10 - 20℃; Large scale;88.94%
With potassium carbonate In water; acetone at 15℃; Product distribution / selectivity;
5-aminomethyl-2-[(3S)-3-methyl-2,6-dioxo-piperidin-3-yl]-isoindole-1,3-dione hydrochloride
1010100-25-0

5-aminomethyl-2-[(3S)-3-methyl-2,6-dioxo-piperidin-3-yl]-isoindole-1,3-dione hydrochloride

n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

{2-[(3S)-3-methyl-2,6-dioxo-piperidin-3-yl]-1,3-dioxo-2,3-dihydro-1H-isoindol-5-ylmethyl}-carbamic acid hexyl ester

{2-[(3S)-3-methyl-2,6-dioxo-piperidin-3-yl]-1,3-dioxo-2,3-dihydro-1H-isoindol-5-ylmethyl}-carbamic acid hexyl ester

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In acetonitrile at 20℃; for 1h;88%
n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

3-({2-[(4-carbamimidoylphenylamino)methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}pyridin-2-yl-amino)propionic acid ethyl ester

3-({2-[(4-carbamimidoylphenylamino)methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}pyridin-2-yl-amino)propionic acid ethyl ester

dabigatran etexilate
211915-06-9

dabigatran etexilate

Conditions
ConditionsYield
With potassium carbonate In water; acetone at 10 - 25℃;88%
Stage #1: 3-({2-[(4-carbamimidoylphenylamino)methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}pyridin-2-yl-amino)propionic acid ethyl ester With potassium carbonate In tetrahydrofuran; water at 20℃; for 0.5h;
Stage #2: n-hexyl chloroformate In tetrahydrofuran; water at 10℃; for 2h;		78%
n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

ethyl 2-{[(4-{carbamimidoyl}phenyl)amino]methyl}-1-methyl-1H-benzimidazol-5-carboxylate
1408238-41-4

ethyl 2-{[(4-{carbamimidoyl}phenyl)amino]methyl}-1-methyl-1H-benzimidazol-5-carboxylate

ethyl 2-[[4-[(n-hexyloxycarbonyl)aminoiminomethyl]phenylamino]methyl]-1-methyl-1H-benzimidazole-5-carboxylate
1408238-36-7

ethyl 2-[[4-[(n-hexyloxycarbonyl)aminoiminomethyl]phenylamino]methyl]-1-methyl-1H-benzimidazole-5-carboxylate

Conditions
ConditionsYield
With sodium hydroxide In water; acetone at 10 - 25℃;87%
n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

1-methyl-2-[N-(4-amidinophenyl)aminomethyl]benzimidazole-5-ylcarboxylic acid N-(2-pyridyl)-N-(2-ethoxycarbonylethyl)amide hydrochloride salt

1-methyl-2-[N-(4-amidinophenyl)aminomethyl]benzimidazole-5-ylcarboxylic acid N-(2-pyridyl)-N-(2-ethoxycarbonylethyl)amide hydrochloride salt

dabigatran etexilate
211915-06-9

dabigatran etexilate

Conditions
ConditionsYield
With sodium hydroxide In water; acetone at 20℃; for 1h; Reagent/catalyst;86.4%
Stage #1: 3-({2-[(4-carbamimidoyl-phenylamino)methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}pyridin-2-ylamino)propionic acid ethyl ester hydrochloride With potassium carbonate In tetrahydrofuran; water at 0 - 5℃; for 0.5h;
Stage #2: n-hexyl chloroformate In tetrahydrofuran; water at 0 - 5℃;		72.7%
With triethylamine In water; acetonitrile at 15℃;
n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

p-aminobenzamidine
3858-83-1

p-aminobenzamidine

hexyl ((4-aminophenyl)(imino)methyl)carbamate

hexyl ((4-aminophenyl)(imino)methyl)carbamate

Conditions
ConditionsYield
With sodium hydroxide In acetone at 0 - 10℃;85.9%
n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

methyl (2RS)-2-(6-chloro-9H-carbazol-2-yl)propanoate
52263-88-4

methyl (2RS)-2-(6-chloro-9H-carbazol-2-yl)propanoate

hexyl 6-chloro-2-(1-methoxy-1-oxoprop-2-yl)-9H-carbazole-9-carboxylate

hexyl 6-chloro-2-(1-methoxy-1-oxoprop-2-yl)-9H-carbazole-9-carboxylate

Conditions
ConditionsYield
With dmap; triethylamine In tetrahydrofuran at 100℃; for 3h; Microwave irradiation;85%
n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

ethyl N-[(2-{[(4-carbamimidoylphenyl)amino]methyl}-1-methyl-1H-benzimidazole-5-yl)carbonyl]-N-(pyridine-2-yl)-β-alaninate bis(p-toluenesulfonic acid salt)

ethyl N-[(2-{[(4-carbamimidoylphenyl)amino]methyl}-1-methyl-1H-benzimidazole-5-yl)carbonyl]-N-(pyridine-2-yl)-β-alaninate bis(p-toluenesulfonic acid salt)

dabigatran etexilate
211915-06-9

dabigatran etexilate

Conditions
ConditionsYield
With potassium carbonate In ethanol; water; acetone at 28 - 32℃; for 0.333333h;85%
With potassium carbonate In ethanol; water; acetone at 28 - 32℃; for 0.333333h;85%
n-hexyl chloroformate
6092-54-2

n-hexyl chloroformate

4-nitrobenzamide
619-80-7

4-nitrobenzamide

4-[[[(hexyloxy)carbonyl]amino]carbonyl]nitrobenzene

4-[[[(hexyloxy)carbonyl]amino]carbonyl]nitrobenzene

Conditions
ConditionsYield
With sodium hydride In tetrahydrofuran for 2h;85%

Hexyl chloroformate Specification

The Carbonochloridic acid,hexyl ester, with CAS registry number 6092-54-2, belongs to the following product categories: (1)Acid Halides; (2)Carbonyl Compounds; (3)Organic Building Blocks. It has the systematic name of hexyl carbonochloridate. This chemical is a kind of clear colorless liquid. And the chemical formula of this chemical is C7H13ClO2.

Physical properties of Carbonochloridic acid,hexyl ester: (1)ACD/LogP: 3.57; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 3.57; (4)ACD/LogD (pH 7.4): 3.57; (5)ACD/BCF (pH 5.5): 301.95; (6)ACD/BCF (pH 7.4): 301.95; (7)ACD/KOC (pH 5.5): 2073.69; (8)ACD/KOC (pH 7.4): 2073.69; (9)#H bond acceptors: 2; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 6; (12)Polar Surface Area: 26.3 Å2; (13)Index of Refraction: 1.43; (14)Molar Refractivity: 41.1 cm3; (15)Molar Volume: 158.9 cm3; (16)Polarizability: 16.29×10-24cm3; (17)Surface Tension: 30.5 dyne/cm; (18)Density: 1.035 g/cm3; (19)Flash Point: 56.3 °C; (20)Enthalpy of Vaporization: 42.34 kJ/mol; (21)Boiling Point: 187.2 °C at 760 mmHg; (22)Vapour Pressure: 0.637 mmHg at 25°C.

Uses of p-Chloropropiophenone: it can be used to produce 2-hexyloxycarbonylamino-3-phenyl-proπonic acid. The yield is about 70%.

When you are using this chemical, please be cautious about it as the following:
The Carbonochloridic acid,hexyl ester is toxic by inhalation, in contact with skin and if swallowed. And this chemical may cause burns. When use it, wear suitable protective clothing, gloves and eye/face protection. After usinf it, take off immediately all contaminated clothing. If contact with eyes, rinse immediately with plenty of water and seek medical advice.

You can still convert the following datas into molecular structure:
(1)SMILES: ClC(=O)OCCCCCC
(2)InChI: InChI=1/C7H13ClO2/c1-2-3-4-5-6-10-7(8)9/h2-6H2,1H3
(3)InChIKey: KIWBRXCOTCXSSZ-UHFFFAOYAB
(4)Std. InChI: InChI=1S/C7H13ClO2/c1-2-3-4-5-6-10-7(8)9/h2-6H2,1H3
(5)Std. InChIKey: KIWBRXCOTCXSSZ-UHFFFAOYSA-N

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