Product Name

  • Name

    Chloromethyl isopropyl carbonate

  • EINECS 1308068-626-2
  • CAS No. 35180-01-9
  • Article Data26
  • CAS DataBase
  • Density 1.15 g/cm3
  • Solubility
  • Melting Point
  • Formula C5H9ClO3
  • Boiling Point 147.5 °C at 760 mmHg
  • Molecular Weight 152.578
  • Flash Point 50 °C
  • Transport Information
  • Appearance Colorless and transparent liquid
  • Safety 24/25
  • Risk Codes
  • Molecular Structure Molecular Structure of 35180-01-9 (Chloromethyl isopropyl carbonate)
  • Hazard Symbols
  • Synonyms Chloromethyl1-methylethyl carbonate;Isopropoxycarbonyloxymethyl chloride;Isopropyl chloromethyl carbonate;[(Isopropyloxycarbonyl)oxy]methyl chloride;
  • PSA 35.53000
  • LogP 1.74430

Synthetic route

carbonochloridic acid, chloromethyl ester
22128-62-7

carbonochloridic acid, chloromethyl ester

isopropyl alcohol
67-63-0

isopropyl alcohol

chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

Conditions
ConditionsYield
With triethylamine at 0℃;98%
With pyridine In diethyl ether; isopropyl alcohol at 10℃; for 18h; Cooling;95%
With pyridine In diethyl ether at 0 - 20℃;92%
formaldehyd
50-00-0

formaldehyd

isopropyl chloroformate
108-23-6

isopropyl chloroformate

chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

Conditions
ConditionsYield
With 1-ethyl-3-methylimidazolium tetrafluoroborate In toluene at 10℃; Reagent/catalyst; Solvent; Temperature;95%
chloromethyl formate
30566-31-5

chloromethyl formate

isopropyl alcohol
67-63-0

isopropyl alcohol

chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

isopropyloxycarbonyloxymethyl iodide
258841-42-8

isopropyloxycarbonyloxymethyl iodide

Conditions
ConditionsYield
With sodium iodide In acetonitrile at 60℃; for 3h;99%
With sodium hydrogencarbonate; sodium iodide In acetone92%
With sodium iodide In acetonitrile at 30℃; for 22h; Inert atmosphere;91.5%
chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

(3S)-1-[(2R)-2-[4-(2-chloro-4-fluorophenyl)-2-oxochromen-7-yl]oxypropanoyl]piperidine-3-carboxylic acid

(3S)-1-[(2R)-2-[4-(2-chloro-4-fluorophenyl)-2-oxochromen-7-yl]oxypropanoyl]piperidine-3-carboxylic acid

isopropoxycarbonyloxymethyl (3S)-1-[(2R)-2-[4-(2-chloro-4-fluorophenyl)-2-oxochromen-7-yl]oxypropanoyl]piperidine-3-carboxylate

isopropoxycarbonyloxymethyl (3S)-1-[(2R)-2-[4-(2-chloro-4-fluorophenyl)-2-oxochromen-7-yl]oxypropanoyl]piperidine-3-carboxylate

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 50℃; for 0.5h;93%
3-[[3-ethyl-1,2,3,6-tetrahydro-5-(1-methylethyl)-2,6-dioxo-4-pyrimidinyl]carbonyl]-5-methylbenzonitrile
1097628-00-6

3-[[3-ethyl-1,2,3,6-tetrahydro-5-(1-methylethyl)-2,6-dioxo-4-pyrimidinyl]carbonyl]-5-methylbenzonitrile

chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

C23H27N3O6
1099828-46-2

C23H27N3O6

Conditions
ConditionsYield
With sodium hydride In N,N-dimethyl-formamide92%
chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

tenofovir
147127-20-6

tenofovir

tenofovir disoproxil

tenofovir disoproxil

Conditions
ConditionsYield
With tetrabutylammomium bromide; triethylamine In 1-methyl-pyrrolidin-2-one at 50℃; Temperature;91.5%
With triethylamine; N-butylpyridinium tetrafluoroborate at 40℃; for 1.5h; Reagent/catalyst; Temperature;90.6%
Stage #1: tenofovir With tetrabutylammomium bromide; triethylamine In 1-methyl-pyrrolidin-2-one at 50℃; for 0.5h;
Stage #2: chloromethyl isopropyl carbonate In 1-methyl-pyrrolidin-2-one at 60℃; for 4h; Reagent/catalyst; Solvent;		87.6%
chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

1-[3-[allyl(methoxy)phosphoryl]oxypropoxy]hexadecane
1258789-65-9

1-[3-[allyl(methoxy)phosphoryl]oxypropoxy]hexadecane

HDP-POC allylphosphonate
1258789-66-0

HDP-POC allylphosphonate

Conditions
ConditionsYield
With sodium iodide In acetonitrile for 72h; Reflux; Inert atmosphere;91%
With sodium iodide In acetonitrile for 72h; Reflux; Inert atmosphere;
chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

(2E)-but-2-enedioic acid
110-17-8

(2E)-but-2-enedioic acid

tenofovir
147127-20-6

tenofovir

tenofovir disoproxyl fumarate
202138-50-9

tenofovir disoproxyl fumarate

Conditions
ConditionsYield
Stage #1: tenofovir With triethylamine In 1-methyl-pyrrolidin-2-one at 63℃; for 0.5h;
Stage #2: chloromethyl isopropyl carbonate In 1-methyl-pyrrolidin-2-one at 63℃; for 4h;
Stage #3: (2E)-but-2-enedioic acid In isopropyl alcohol at 50℃; for 0.5h; Concentration;		90%
Stage #1: chloromethyl isopropyl carbonate; tenofovir With tetrabutylammomium bromide; triethylamine at 50℃; for 3h; Inert atmosphere;
Stage #2: (2E)-but-2-enedioic acid In isopropyl alcohol Reagent/catalyst; Temperature; Reflux;		78.8%
Stage #1: chloromethyl isopropyl carbonate; tenofovir With tetrabutylammomium bromide; triethylamine In 1-methyl-pyrrolidin-2-one; toluene at 45 - 55℃; for 5h;
Stage #2: (2E)-but-2-enedioic acid In isopropyl alcohol at 50 - 55℃; for 2h;		63.6%
...Expand
R-361015

R-361015

chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

C21H26ClNO7S

C21H26ClNO7S

Conditions
ConditionsYield
With thionyl chloride at 80℃; for 4h;87%
chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

benzylamine
100-46-9

benzylamine

isopropyl N-benzylcarbamate
5338-49-8

isopropyl N-benzylcarbamate

Conditions
ConditionsYield
In benzene a.) RT, 1 h, b.) reflux, 1 h;85.4%
chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

C16H28N5O7P

C16H28N5O7P

C26H44N5O13P

C26H44N5O13P

Conditions
ConditionsYield
With triethylamine In 1-methyl-pyrrolidin-2-one; ethanol at 20 - 55℃; for 6h;85.4%
chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

1-[(2'-t-butoxycarbonylbiphenyl-4-yl)methyl]-4-(1-hydroxy-1-methylethyl)-2-propylimidazole-5-carboxylic acid
144690-41-5

1-[(2'-t-butoxycarbonylbiphenyl-4-yl)methyl]-4-(1-hydroxy-1-methylethyl)-2-propylimidazole-5-carboxylic acid

isopropoxycarbonyloxymethyl 1-[(2'-t-butoxycarbonylbiphenyl-4-yl)methyl]-4-(1-hydroxy-1-methylethyl)-2-propylimidazole-5carboxylate
144690-43-7

isopropoxycarbonyloxymethyl 1-[(2'-t-butoxycarbonylbiphenyl-4-yl)methyl]-4-(1-hydroxy-1-methylethyl)-2-propylimidazole-5carboxylate

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl acetamide at 20 - 50℃; for 3h;85%
chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

5-((4'-isopropyl-[1,1'-biphenyl]-4-yl)oxy)-1-(4-methoxybenzyl)-1H-1,2,3-triazole-4-carboxylic acid

5-((4'-isopropyl-[1,1'-biphenyl]-4-yl)oxy)-1-(4-methoxybenzyl)-1H-1,2,3-triazole-4-carboxylic acid

((isopropoxycarbonyl)oxy)methyl 5-((4'-isopropyl-[1,1'-biphenyl]-4-yl)oxy)-1-(4-methoxybenzyl)-1H-1,2,3-triazole-4-carboxylate

((isopropoxycarbonyl)oxy)methyl 5-((4'-isopropyl-[1,1'-biphenyl]-4-yl)oxy)-1-(4-methoxybenzyl)-1H-1,2,3-triazole-4-carboxylate

Conditions
ConditionsYield
Stage #1: 5-((4'-isopropyl-[1,1'-biphenyl]-4-yl)oxy)-1-(4-methoxybenzyl)-1H-1,2,3-triazole-4-carboxylic acid With potassium carbonate In N,N-dimethyl acetamide at 20℃; for 0.5h;
Stage #2: chloromethyl isopropyl carbonate In N,N-dimethyl acetamide at 50℃; for 6h;		84.1%
chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

5-(3-methylbut-1-ynyl)-3-[(trans-4-methylcyclohexanecarbonyl)-[(1S)-1-(morpholine-4-carbonyl)propyl]amino]thiophene-2-carboxylic acid.

5-(3-methylbut-1-ynyl)-3-[(trans-4-methylcyclohexanecarbonyl)-[(1S)-1-(morpholine-4-carbonyl)propyl]amino]thiophene-2-carboxylic acid.

C32H46N2O8S

C32H46N2O8S

Conditions
ConditionsYield
With potassium carbonate; sodium iodide In N,N-dimethyl-formamide at 80℃; for 0.333333h; Microwave irradiation;83%
chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

3-[[(1S)-1-(dimethylcarbamoyl)propyl]-(trans-4-methylcyclohexanecarbonyl)amino]-5-(3-methylbut-1-ynyl)thiophene-2-carboxylic acid

3-[[(1S)-1-(dimethylcarbamoyl)propyl]-(trans-4-methylcyclohexanecarbonyl)amino]-5-(3-methylbut-1-ynyl)thiophene-2-carboxylic acid

C31H46N2O6S

C31H46N2O6S

Conditions
ConditionsYield
With potassium carbonate; sodium iodide In N,N-dimethyl-formamide at 80℃; for 0.333333h; Microwave irradiation;80%
chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

N-(3-(3,6-difluoropyridin-2-yl)-1-((1r,4r)-4-ethoxycyclohexyl)-1H-pyrazol-4-yl)-2-(1H-pyrazol-4-yl)thiazole-4-carboxamide

N-(3-(3,6-difluoropyridin-2-yl)-1-((1r,4r)-4-ethoxycyclohexyl)-1H-pyrazol-4-yl)-2-(1H-pyrazol-4-yl)thiazole-4-carboxamide

(4-(4-((3-(3,6-difluoropyridin-2-yl)-1-((1r,4r)-4-ethoxycyclohexyl)-1H-pyrazol-4-yl)carbamoyl)thiazol-2-yl)-1H-pyrazol-1-yl)methyl isopropyl carbonate

(4-(4-((3-(3,6-difluoropyridin-2-yl)-1-((1r,4r)-4-ethoxycyclohexyl)-1H-pyrazol-4-yl)carbamoyl)thiazol-2-yl)-1H-pyrazol-1-yl)methyl isopropyl carbonate

Conditions
ConditionsYield
With caesium carbonate In N,N-dimethyl-formamide at 20℃;80%
With caesium carbonate In N,N-dimethyl-formamide at 20℃;80%
chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

5-(3,3-dimethylbut-1-ynyl)-3-[(trans-4-methylcyclohexanecarbonyl)-(2-oxo-2-thiomorpholino-ethyl)amino]thiophene-2-carboxylic acid

5-(3,3-dimethylbut-1-ynyl)-3-[(trans-4-methylcyclohexanecarbonyl)-(2-oxo-2-thiomorpholino-ethyl)amino]thiophene-2-carboxylic acid

C30H42N2O8S

C30H42N2O8S

Conditions
ConditionsYield
With potassium carbonate; sodium iodide In N,N-dimethyl-formamide at 80℃; for 0.333333h; Microwave irradiation;76%
chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

(1S,2R,3S,4S,5R,6R)-2-[(tert-butoxycarbonyl)amino]-3-[(3,4-dichlorobenzyl)oxy]-4-hydroxybicyclo[3.1.0]hexane-2,6-dicarboxylic acid
1377990-58-3

(1S,2R,3S,4S,5R,6R)-2-[(tert-butoxycarbonyl)amino]-3-[(3,4-dichlorobenzyl)oxy]-4-hydroxybicyclo[3.1.0]hexane-2,6-dicarboxylic acid

bis({[(1-methylethoxy)carbonyl]oxy}methyl) (1S,2R,3S,4S,5R,6R)-2-[(tert-butoxycarbonyl)amino]-3-[(3,4-dichlorobenzyl)oxy]-4-hydroxybicyclo[3.1.0]hexane-2,6-dicarboxylate
1377990-61-8

bis({[(1-methylethoxy)carbonyl]oxy}methyl) (1S,2R,3S,4S,5R,6R)-2-[(tert-butoxycarbonyl)amino]-3-[(3,4-dichlorobenzyl)oxy]-4-hydroxybicyclo[3.1.0]hexane-2,6-dicarboxylate

Conditions
ConditionsYield
With potassium carbonate; sodium iodide In N,N-dimethyl-formamide for 18h; Product distribution / selectivity;76%
chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

tenofovir
147127-20-6

tenofovir

Tenofovir mono-POC

Tenofovir mono-POC

Conditions
ConditionsYield
With triethylamine In N,N-dimethyl-formamide at 20 - 40℃; for 12h; Temperature;76%
chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

C12H20N5O4P

C12H20N5O4P

propan-2-yl {[(propan-2-yloxy)carbonyl]oxy}methyl {[(2R)-1-(6-amino-9H-purin-9-yl)propan-2-yl]oxy}methanephosphonate

propan-2-yl {[(propan-2-yloxy)carbonyl]oxy}methyl {[(2R)-1-(6-amino-9H-purin-9-yl)propan-2-yl]oxy}methanephosphonate

Conditions
ConditionsYield
With triethylamine In N,N-dimethyl-formamide at 45 - 50℃; for 1h;75.6%
allylphosphonic acid dimethyl ester
757-54-0

allylphosphonic acid dimethyl ester

chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

bis-POC-allylphosphonate
1258789-64-8

bis-POC-allylphosphonate

Conditions
ConditionsYield
With sodium iodide In acetonitrile for 72h; Inert atmosphere; Reflux;75%
With sodium iodide In acetonitrile for 48h; Reflux; Inert atmosphere;5.75 g
formic acid
64-18-6

formic acid

4-((6bR,10aS)-3-methyl-2,3,6b,9,10,10a-hexahydro-1H-pyrido-[3’,4’:4,5]-pyrrolo[1,2,3-de]quinoxalin-8-(7H)-yl)-1-(4-fluorophenyl)-1-butanone
313368-91-1

4-((6bR,10aS)-3-methyl-2,3,6b,9,10,10a-hexahydro-1H-pyrido-[3’,4’:4,5]-pyrrolo[1,2,3-de]quinoxalin-8-(7H)-yl)-1-(4-fluorophenyl)-1-butanone

chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

(6bR,10aS)-8-[4-(4-fluoro-phenyl)-4-oxo-butyl]-8-isopropoxycarbonyloxymethyl-3-methyl-2,3,6b,7,8,9,10,10a-octahydro-1H-pyrido[3',4':4,5]pyrrolo[1,2,3-de]quinoxalin-8-ium formate

(6bR,10aS)-8-[4-(4-fluoro-phenyl)-4-oxo-butyl]-8-isopropoxycarbonyloxymethyl-3-methyl-2,3,6b,7,8,9,10,10a-octahydro-1H-pyrido[3',4':4,5]pyrrolo[1,2,3-de]quinoxalin-8-ium formate

Conditions
ConditionsYield
Stage #1: 4-((6bR,10aS)-3-methyl-2,3,6b,9,10,10a-hexahydro-1H-pyrido-[3’,4’:4,5]-pyrrolo[1,2,3-de]quinoxalin-8-(7H)-yl)-1-(4-fluorophenyl)-1-butanone; chloromethyl isopropyl carbonate With sodium iodide In acetonitrile at 20℃; for 168h;
Stage #2: formic acid In water; acetonitrile for 0.366667h;		75%
...Expand
chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

{[(4-methylbenzenesulfonyl)oxy]methyl}phosphonic acid
161760-09-4

{[(4-methylbenzenesulfonyl)oxy]methyl}phosphonic acid

C18H27O12PS

C18H27O12PS

Conditions
ConditionsYield
Stage #1: tosyloxymethylphosphonic acid monoethyl ester With triethylamine In N,N-dimethyl-formamide at 20℃; for 1h;
Stage #2: chloromethyl isopropyl carbonate In N,N-dimethyl-d6-formamide at 60℃; for 5h; Solvent; Reagent/catalyst;		75%
3-tert-Butyl-4-hydroxyanisole
121-00-6

3-tert-Butyl-4-hydroxyanisole

chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

(2-tert-butyl-4-methoxyphenoxy)methyl carbonate isopropyl ester

(2-tert-butyl-4-methoxyphenoxy)methyl carbonate isopropyl ester

Conditions
ConditionsYield
Stage #1: 3-tert-Butyl-4-hydroxyanisole With sodium hydride In tetrahydrofuran for 0.5h;
Stage #2: chloromethyl isopropyl carbonate In tetrahydrofuran at 20℃; for 24h;		75%
chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

C17H25O7P

C17H25O7P

5-benzyl 1-(((isopropoxycarbonyl)oxy)methyl) 2-((diethoxyphosphoryl)methyl)pentanedioate

5-benzyl 1-(((isopropoxycarbonyl)oxy)methyl) 2-((diethoxyphosphoryl)methyl)pentanedioate

Conditions
ConditionsYield
Stage #1: C17H25O7P With potassium carbonate; sodium iodide In acetonitrile at 20℃; for 0.25h;
Stage #2: chloromethyl isopropyl carbonate In acetonitrile at 50℃;		72%
chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

6-chloro-7-methoxy-2-methyl-3-(4-(4-(trifluoromethoxy)phenoxy)phenyl)quinolin-4(1H)-one
1354745-52-0

6-chloro-7-methoxy-2-methyl-3-(4-(4-(trifluoromethoxy)phenoxy)phenyl)quinolin-4(1H)-one

ELQ-330

ELQ-330

Conditions
ConditionsYield
With tetra-(n-butyl)ammonium iodide; potassium carbonate In N,N-dimethyl-formamide at 60℃; for 2h; Inert atmosphere;72%
With tetra-(n-butyl)ammonium iodide; potassium carbonate In N,N-dimethyl-formamide at 60℃;
chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

C12H11ClN2O2

C12H11ClN2O2

C17H19ClN2O5

C17H19ClN2O5

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 3h;70.5%
chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

5-(3,3-dimethylbut-1-yn-1-yl)-3-(4-methyl-N-((S)-1-methyl-2-oxoazepan-3-yl)cyclohexanecarboxamido)thiophene-2-carboxylic acid

5-(3,3-dimethylbut-1-yn-1-yl)-3-(4-methyl-N-((S)-1-methyl-2-oxoazepan-3-yl)cyclohexanecarboxamido)thiophene-2-carboxylic acid

C31H44N2O7S

C31H44N2O7S

Conditions
ConditionsYield
With potassium carbonate; sodium iodide In N,N-dimethyl-formamide at 80℃; for 0.5h; Microwave irradiation;70%
chloromethyl isopropyl carbonate
35180-01-9

chloromethyl isopropyl carbonate

(1S,2R,3S,4S,5R,6R)-2-[(tert-butoxycarbonyl)amino]-3-{[(3,4-difluorophenyl)sulfanyl]methyl}-4-hydroxybicyclo[3.1.0]hexane-2,6-dicarboxylic acid
1377615-94-5

(1S,2R,3S,4S,5R,6R)-2-[(tert-butoxycarbonyl)amino]-3-{[(3,4-difluorophenyl)sulfanyl]methyl}-4-hydroxybicyclo[3.1.0]hexane-2,6-dicarboxylic acid

bis({[(1-methylethoxy)carbonyl]oxy}methyl) (1S,2R,3S,4S,5R,6R)-2-[(tert-butoxycarbonyl)amino]-3-{[(3,4-difluorophenyl)sulfanyl]methyl}-4-hydroxybicyclo[3.1.0]hexane-2,6-dicarboxylate
1377616-01-7

bis({[(1-methylethoxy)carbonyl]oxy}methyl) (1S,2R,3S,4S,5R,6R)-2-[(tert-butoxycarbonyl)amino]-3-{[(3,4-difluorophenyl)sulfanyl]methyl}-4-hydroxybicyclo[3.1.0]hexane-2,6-dicarboxylate

Conditions
ConditionsYield
With potassium carbonate; sodium iodide In N,N-dimethyl-formamide at 25℃; for 12h; Product distribution / selectivity; Inert atmosphere;70%

Chloromethyl isopropyl carbonate Specification

The Chloromethyl isopropyl carbonate, with the CAS registry number 35180-01-9, is also known as Chloromethyl (1-methylethyl) carbonate. It belongs to the product category of Pharmaceutical Intermediates. This chemical's molecular formula is C5H9ClO3 and molecular weight is 152.58. Its IUPAC name is called chloromethyl propan-2-yl carbonate. What's more, this chemical is used as intermediates in organic synthesis.

Physical properties of Chloromethyl isopropyl carbonate: (1)ACD/LogP: 1.32; (2)ACD/LogD (pH 5.5): 1; (3)ACD/LogD (pH 7.4): 1; (4)ACD/BCF (pH 5.5): 5; (5)ACD/BCF (pH 7.4): 5; (6)ACD/KOC (pH 5.5): 115; (7)ACD/KOC (pH 7.4): 115; (8)#H bond acceptors: 3; (9)#Freely Rotating Bonds: 4; (10)Index of Refraction: 1.42; (11)Molar Refractivity: 33.541 cm3; (12)Molar Volume: 132.675 cm3; (13)Surface Tension: 30.309 dyne/cm; (14)Density: 1.15 g/cm3; (15)Flash Point: 49.952 °C; (16)Enthalpy of Vaporization: 38.444 kJ/mol; (17)Boiling Point: 147.463 °C at 760 mmHg; (18)Vapour Pressure: 4.419 mmHg at 25°C.

You can still convert the following datas into molecular structure:
(1)Canonical SMILES: CC(C)OC(=O)OCCl
(2)InChI: InChI=1S/C5H9ClO3/c1-4(2)9-5(7)8-3-6/h4H,3H2,1-2H3
(3)InChIKey: JHYNXXBAHWPABC-UHFFFAOYSA-N

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