Product Name

  • Name

    1 -Chloro-2-propanol

  • EINECS 204-819-6
  • CAS No. 127-00-4
  • Article Data109
  • CAS DataBase
  • Density 1.083 g/cm3
  • Solubility
  • Melting Point
  • Formula C3H7ClO
  • Boiling Point 126.499 °C at 760 mmHg
  • Molecular Weight 94.541
  • Flash Point 54.541 °C
  • Transport Information UN 2611 6.1/PG 2
  • Appearance colourless to light yellow liquid
  • Safety 26-36/39
  • Risk Codes 10-20-36/37/38
  • Molecular Structure Molecular Structure of 127-00-4 (1 -Chloro-2-propanol)
  • Hazard Symbols HarmfulXn
  • Synonyms 1-Chloro-2-hydroxypropane;1-Chloroisopropyl alcohol;NSC77373;sec-Propylene chlorohydrin;a-Propylene chlorohydrin;
  • PSA 20.23000
  • LogP 0.60600

Synthetic route

methyloxirane
75-56-9, 16033-71-9

methyloxirane

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

Conditions
ConditionsYield
With chloro-trimethyl-silane; 3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate at 20℃; for 1h; ring opening reaction;97%
With chloro-trimethyl-silane; zinc(II) oxide In dichloromethane at 20℃; for 0.5h; regioselective reaction;85%
With chlorine
methyloxirane
75-56-9, 16033-71-9

methyloxirane

A

2-chloro-1-propanol
78-89-7

2-chloro-1-propanol

B

allyl alcohol
107-18-6

allyl alcohol

C

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

Conditions
ConditionsYield
With hydrogenchloride In solid at 60 - 70℃; for 7h; in tri-o-thymotide clathrate;A 5%
B 87%
C 8%
chloroacetone
78-95-5

chloroacetone

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

Conditions
ConditionsYield
With sodium tetrahydroborate Reduction;85%
With tris(pentafluorophenyl)borate; hydrogen In diethyl ether at 70℃; under 45603.1 Torr; for 12h; Solvent; Glovebox;85%
Stage #1: chloroacetone With sodium tetrahydroborate In ethanol at 20℃; Cooling with ice;
Stage #2: With hydrogenchloride In ethanol; water
50%
propene
187737-37-7

propene

A

2-chloro-1-propanol
78-89-7

2-chloro-1-propanol

B

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

Conditions
ConditionsYield
With chlorourea; acetic acidA n/a
B 80%
With hypochloric acid
With sulfuric acid; chloroamine-T In water; acetone at 50℃; Yield given. Yields of byproduct given;
epichlorohydrin
106-89-8

epichlorohydrin

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

Conditions
ConditionsYield
With morpholine-borane; boron trifluoride diethyl etherate In diethyl ether for 2h; Product distribution; Ambient temperature;80%
With Bu3Sn(tripiperidinophosphine oxide)I; tri-n-butyl-tin hydride In tetrahydrofuran at 60℃; for 1h;77%
With ethanol; nickel Hydrogenation.unter Druck;
2-hydroxypropyl perchlorate
88504-84-1

2-hydroxypropyl perchlorate

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

Conditions
ConditionsYield
With lithium chloride In tetrachloromethane; acetone for 1h;80%
methyloxirane
75-56-9, 16033-71-9

methyloxirane

A

2-chloro-1-propanol
78-89-7

2-chloro-1-propanol

B

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

Conditions
ConditionsYield
With ammonium cerium(IV) nitrate; tri-n-butyl benzyl ammonium chloride In acetonitrile for 3h; Ambient temperature;A 70%
B 18%
With hydrogenchloride
With pyridine hydrochloride In chloroform for 1h; Ambient temperature;A 18 % Chromat.
B 68 % Chromat.
Stage #1: methyloxirane With chromyl chloride In dichloromethane at -50℃; for 2h; Ring cleavage;
Stage #2: With water In dichloromethane at -50 - 20℃; Hydrolysis;
methanol
67-56-1

methanol

methyloxirane
75-56-9, 16033-71-9

methyloxirane

A

1-methoxy-2-propanol
107-98-2

1-methoxy-2-propanol

B

2-methoxypropanol
1589-47-5

2-methoxypropanol

C

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

Conditions
ConditionsYield
With Cu(L-Asp)(1,2-bis(4-pyridyl)ethylene)0.5(H2O)0.5(MeOH)0.5 at 25℃;A 56%
B 40%
C 4%
With Cu(L-Asp)(1,2-bis(4-pyridyl)ethylene)0.5(H2O)0.5(MeOH)0.5 at 60℃;A 49%
B 47%
C 4%
propene
187737-37-7

propene

A

1-chloro-2-acetoxypropane
623-60-9

1-chloro-2-acetoxypropane

B

N-(2-Chloro-1-methyl-ethyl)-4-methyl-benzenesulfonamide

N-(2-Chloro-1-methyl-ethyl)-4-methyl-benzenesulfonamide

C

toluene-4-sulfonamide
70-55-3

toluene-4-sulfonamide

D

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

E

CH3COONa

CH3COONa

Conditions
ConditionsYield
With chloroamine-T; acetic acid at 50 - 60℃; for 3h;A 43%
B 17%
C n/a
D 10%
E n/a
propene
187737-37-7

propene

acetic acid
64-19-7

acetic acid

A

1-chloro-2-acetoxypropane
623-60-9

1-chloro-2-acetoxypropane

B

N-(2-Chloro-1-methyl-ethyl)-4-methyl-benzenesulfonamide

N-(2-Chloro-1-methyl-ethyl)-4-methyl-benzenesulfonamide

C

toluene-4-sulfonamide
70-55-3

toluene-4-sulfonamide

D

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

E

CH3COONa

CH3COONa

Conditions
ConditionsYield
With chloroamine-T at 50 - 60℃; for 3h;A 43%
B 17%
C n/a
D 10%
E n/a
propene
187737-37-7

propene

chloramine T trihydrate
7080-50-4

chloramine T trihydrate

A

1-chloro-2-acetoxypropane
623-60-9

1-chloro-2-acetoxypropane

B

N-(2-Chloro-1-methyl-ethyl)-4-methyl-benzenesulfonamide

N-(2-Chloro-1-methyl-ethyl)-4-methyl-benzenesulfonamide

C

toluene-4-sulfonamide
70-55-3

toluene-4-sulfonamide

D

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

E

CH3COONa

CH3COONa

Conditions
ConditionsYield
With acetic acid at 50 - 60℃; for 3h;A 43%
B 17%
C n/a
D 10%
E n/a
propylene glycol
57-55-6

propylene glycol

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

Conditions
ConditionsYield
With hydrogenchloride
With tetrachlorosilane
With sulphur monochloride
propene
187737-37-7

propene

tert-butylhypochlorite
507-40-4

tert-butylhypochlorite

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

Conditions
ConditionsYield
With water at 18 - 42℃;
propene
187737-37-7

propene

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

Conditions
ConditionsYield
With water; chlorine
With water; chlorine; copper dichloride
With hypochloric acid
2-amino-1-chloropropane
37143-56-9

2-amino-1-chloropropane

A

2-chloro-1-propanol
78-89-7

2-chloro-1-propanol

B

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

Conditions
ConditionsYield
With cis-nitrous acid
3-chloroprop-1-ene
107-05-1

3-chloroprop-1-ene

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

Conditions
ConditionsYield
With sulfuric acid
With [Ru(II)(2,2':6',2''-terpyridine)(quinaldic acid(1-))Cl]; 3-chloro-benzenecarboperoxoic acid In ethanol for 8h; Inert atmosphere; chemoselective reaction;
2-chloropropylamine
14753-25-4

2-chloropropylamine

A

2-chloro-1-propanol
78-89-7

2-chloro-1-propanol

B

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

Conditions
ConditionsYield
With cis-nitrous acid
1-chloro-3-hydroxypropane
627-30-5

1-chloro-3-hydroxypropane

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

Conditions
ConditionsYield
With 2,4,6-trimethyl-pyridine; 8-quinolinylboronic acid In N,N-dimethyl-formamide
propylene glycol
57-55-6

propylene glycol

A

2-chloro-1-propanol
78-89-7

2-chloro-1-propanol

B

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

C

methyloxirane
75-56-9, 16033-71-9

methyloxirane

Conditions
ConditionsYield
With tert-butylhypochlorite; potassium carbonate; triphenylphosphine In chloroform Product distribution; 1.) -70 deg C, 2.) RT, 3.) reflux, 24 h;
propene
187737-37-7

propene

A

1,2-Dichloropropane
26198-63-0, 78-87-5

1,2-Dichloropropane

B

bis(3-chloropropyl)ether
629-36-7

bis(3-chloropropyl)ether

C

bis(1-chloro-2-propyl) ether
108-60-1

bis(1-chloro-2-propyl) ether

D

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

Conditions
ConditionsYield
With hypochloric acid; chlorine In butanone at 20℃; for 0.00833333h; in a rotor-pulsation apparatus; Title compound not separated from byproducts;A 15.8 % Spectr.
B n/a
C n/a
D 68.6 % Spectr.
With hypochloric acid; chlorine In butanone at 20℃; for 0.00833333h; Product distribution; Mechanism; yield of products at different temperatures and in different solvents, in a rotor-pulsation apparatus;A 15.8 % Spectr.
B n/a
C n/a
D 68.6 % Spectr.
2-chloro-1-propanol
78-89-7

2-chloro-1-propanol

A

propan-1-ol
71-23-8

propan-1-ol

B

1,2-Dichloropropane
26198-63-0, 78-87-5

1,2-Dichloropropane

C

2-(2-chloropropoxy)-1-propanol

2-(2-chloropropoxy)-1-propanol

D

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

Conditions
ConditionsYield
at 180℃; Rate constant; Mechanism; Product distribution;
1-(p-cyanophenyl)3-(2-chloropropyl)triazene
78604-24-7

1-(p-cyanophenyl)3-(2-chloropropyl)triazene

A

2-chloropropene
557-98-2

2-chloropropene

B

2-chloro-1-propanol
78-89-7

2-chloro-1-propanol

C

1,2-Dichloropropane
26198-63-0, 78-87-5

1,2-Dichloropropane

D

acetone
67-64-1

acetone

E

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

F

4-Aminobenzonitrile
873-74-5

4-Aminobenzonitrile

Conditions
ConditionsYield
In water; acetonitrile at 37.5℃; decomposition half-life; pH=7.1;
3-chloroprop-1-ene
107-05-1

3-chloroprop-1-ene

A

allyl alcohol
107-18-6

allyl alcohol

B

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

C

methyloxirane
75-56-9, 16033-71-9

methyloxirane

Conditions
ConditionsYield
With sodium tetrahydroborate; mercury(II) diacetate Product distribution; 2.) EtOH;A 3 % Chromat.
B 70 % Chromat.
C 21 % Chromat.
chloro-trimethyl-silane
75-77-4

chloro-trimethyl-silane

methyloxirane
75-56-9, 16033-71-9

methyloxirane

A

2-chloro-1-propanol
78-89-7

2-chloro-1-propanol

B

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

Conditions
ConditionsYield
With cesium fluoride 1) CH2Cl2, r.t., 2) MeOH, r.t., 1 h; Multistep reaction. Title compound not separated from byproducts;
epichlorohydrin
106-89-8

epichlorohydrin

A

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

B

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

1-chloro-3-hydroxypropane

Conditions
ConditionsYield
With zinc(II) tetrahydroborate; silica gel In tetrahydrofuran for 24h; Product distribution; Ambient temperature; other epoxides;
With zinc(II) tetrahydroborate; silica gel In tetrahydrofuran for 24h; Ambient temperature; Yield given. Yields of byproduct given;
With zeolite supported zinc borohydride In tetrahydrofuran at 20℃; for 12h; Yield given. Yields of byproduct given;
With hydrogen; palladium on activated charcoal In ethyl acetate at 23℃; under 760.051 Torr; for 20h;A 91 % Chromat.
B 9.0 % Chromat.
epichlorohydrin
106-89-8

epichlorohydrin

A

1,3-Dichloro-2-propanol
96-23-1

1,3-Dichloro-2-propanol

B

bis-(4-chlorobutyl)ether
6334-96-9

bis-(4-chlorobutyl)ether

C

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

Conditions
ConditionsYield
With zinc(II) tetrahydroborate; monoaluminum phosphate In tetrahydrofuran for 24h; Product distribution; Ambient temperature; influence of catalyst on degree of epichlorohydrin conversion and reaction selectivity; further catalysts;
hydrogenchloride
7647-01-0

hydrogenchloride

methyloxirane
75-56-9, 16033-71-9

methyloxirane

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

Conditions
ConditionsYield
inactive form;
hydrogenchloride
7647-01-0

hydrogenchloride

diethyl ether
60-29-7

diethyl ether

methyloxirane
75-56-9, 16033-71-9

methyloxirane

A

2-chloro-1-propanol
78-89-7

2-chloro-1-propanol

B

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

Conditions
ConditionsYield
at -55 - 35℃;
hydrogenchloride
7647-01-0

hydrogenchloride

water
7732-18-5

water

methyloxirane
75-56-9, 16033-71-9

methyloxirane

A

2-chloro-1-propanol
78-89-7

2-chloro-1-propanol

B

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

Conditions
ConditionsYield
at 15 - 83℃;
boron trichloride
10294-34-5

boron trichloride

methyloxirane
75-56-9, 16033-71-9

methyloxirane

A

2-chloro-1-propanol
78-89-7

2-chloro-1-propanol

B

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

Conditions
ConditionsYield
anschliessend mit Methanol;
chloro-diphenylphosphine
1079-66-9

chloro-diphenylphosphine

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

(2-chloro-1-methylethoxy)diphenylphosphane
839-95-2

(2-chloro-1-methylethoxy)diphenylphosphane

Conditions
ConditionsYield
With triethylamine In diethyl ether at 0℃; for 0.5h;98%
4-Phenoxyphenol
831-82-3

4-Phenoxyphenol

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

(R,S)-2-hydroxypropyl 4-phenoxyphenyl ether
57650-78-9

(R,S)-2-hydroxypropyl 4-phenoxyphenyl ether

Conditions
ConditionsYield
With sodium hydroxide In water; toluene at 85℃; for 0.166667h; Temperature; Reagent/catalyst;95%
2-nitrothiophenol
4875-10-9

2-nitrothiophenol

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

A

bis[β-(2-nitrophenylthio)-α-methyl-ethyl]-terephthalate

bis[β-(2-nitrophenylthio)-α-methyl-ethyl]-terephthalate

B

1-(2-nitro-phenylsulfanyl)-propan-2-ol
28097-57-6

1-(2-nitro-phenylsulfanyl)-propan-2-ol

Conditions
ConditionsYield
With sodium hydroxide In waterA n/a
B 94.8%
diphenyl(methyl)phosphine
1486-28-8

diphenyl(methyl)phosphine

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

(2-Hydroxypropyl)(methyl)diphenylphosphonium-chlorid
99744-29-3

(2-Hydroxypropyl)(methyl)diphenylphosphonium-chlorid

Conditions
ConditionsYield
In acetonitrile at 75 - 80℃; for 96h;94%
acetic anhydride
108-24-7

acetic anhydride

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

1-chloro-2-acetoxypropane
623-60-9

1-chloro-2-acetoxypropane

Conditions
ConditionsYield
With sodium hydroxide for 0.0208333h; microwave irradiation;94%
With pyridine Acetylation;
phenylthiophosphonic acid dimethyl ester
6840-11-5

phenylthiophosphonic acid dimethyl ester

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

bis(1-chloro-2-propyl) phenylthiophosphonate

bis(1-chloro-2-propyl) phenylthiophosphonate

Conditions
ConditionsYield
With magnesium chloride at 100℃; for 6h; Inert atmosphere;91.1%
(R,R)-(-)-N,N’-bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II)
176763-62-5, 188264-84-8, 371258-71-8, 201556-02-7, 478944-44-4

(R,R)-(-)-N,N’-bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II)

carbon monoxide
201230-82-2

carbon monoxide

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

C40H58ClCoN2O4

C40H58ClCoN2O4

Conditions
ConditionsYield
With dipotassium peroxodisulfate In dichloromethane at 20℃; under 760.051 Torr; Darkness;91%
1,2,5,6-tetrahydrobenzoic acid
4771-80-6

1,2,5,6-tetrahydrobenzoic acid

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

Cyclohex-3-enecarboxylic acid 2-chloro-1-methyl-ethyl ester
145521-36-4

Cyclohex-3-enecarboxylic acid 2-chloro-1-methyl-ethyl ester

Conditions
ConditionsYield
With sulfuric acid In toluene at 130℃;90%
With sulfuric acid In toluene at 90℃; Rate constant;
2-methyl-1,4-naphthohydroquinone
481-85-6

2-methyl-1,4-naphthohydroquinone

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

4-(1-Chlor-2-propoxy)-2-methyl-1-naphthol
99893-97-7

4-(1-Chlor-2-propoxy)-2-methyl-1-naphthol

Conditions
ConditionsYield
With hydrogenchloride at 60℃; for 0.75h;88%
4-methyleneoxetan-2-one
674-82-8

4-methyleneoxetan-2-one

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

3-Oxo-butyric acid 2-chloro-1-methyl-ethyl ester
100426-98-0

3-Oxo-butyric acid 2-chloro-1-methyl-ethyl ester

Conditions
ConditionsYield
at 100 - 120℃; for 4.08333h;86%
1-Octyn-3-ol
818-72-4

1-Octyn-3-ol

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

3-(1-chloropropan-2-yloxy)oct-1-yne
1138163-66-2

3-(1-chloropropan-2-yloxy)oct-1-yne

Conditions
ConditionsYield
Stage #1: 1-Octyn-3-ol With dicobalt octacarbonyl In dichloromethane at 20℃; for 2h; Nicholas reaction; Inert atmosphere;
Stage #2: 1-Chloro-2-propanol With boron trifluoride diethyl etherate In dichloromethane at 0℃; for 1h; Nicholas reaction; Inert atmosphere;
Stage #3: With ammonium cerium (IV) nitrate In acetone at 0℃; Nicholas reaction; Inert atmosphere;
86%
thiophenol
108-98-5

thiophenol

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

1-phenylsulfanyl-propan-2-ol
937-56-4

1-phenylsulfanyl-propan-2-ol

Conditions
ConditionsYield
With sodium hydroxide In ethanol 1.) heating, 30 min, 2.) reflux;85%
4-phenylisoquinolin-1(2H)-one
36828-24-7

4-phenylisoquinolin-1(2H)-one

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

2-(2-hydroxypropyl)-4-phenyl-1(2H)-isoquinolone
84555-22-6

2-(2-hydroxypropyl)-4-phenyl-1(2H)-isoquinolone

Conditions
ConditionsYield
With potassium carbonate In N-methyl-acetamide81%
4-chlorophenylethylamine
156-41-2

4-chlorophenylethylamine

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

1-[[2-(4-chlorophenyl)ethyl]amino]-2-hydroxypropane
847063-13-2

1-[[2-(4-chlorophenyl)ethyl]amino]-2-hydroxypropane

Conditions
ConditionsYield
With potassium carbonate In acetonitrile at 20 - 60℃; Reagent/catalyst; Inert atmosphere;80.1%
2,4-dibromophenol
615-58-7

2,4-dibromophenol

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

(+/-)-1-(2,4-dibromophenoxy)-2-propanol
1224246-01-8

(+/-)-1-(2,4-dibromophenoxy)-2-propanol

Conditions
ConditionsYield
With sodium hydroxide In water for 24h; Reflux;80%
benzoyl chloride
98-88-4

benzoyl chloride

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

1-chloro-2-benzoyloxypropane
36220-92-5

1-chloro-2-benzoyloxypropane

Conditions
ConditionsYield
In pyridine at 20℃; for 2h;79%
at 170℃;
Northiadene
24881-71-8

Northiadene

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

(E)-11-(3-propylidene)-6,11-dihydrodibenzothiepin
85196-00-5

(E)-11-(3-propylidene)-6,11-dihydrodibenzothiepin

Conditions
ConditionsYield
With sodium carbonate In N,N-dimethyl-formamide77%
2-chloro-1-propanol
78-89-7

2-chloro-1-propanol

methyl 3,3,3-trifluoropyruvate
13089-11-7

methyl 3,3,3-trifluoropyruvate

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

2-carboxymethyl-2-trifluoromethyl-4-methyl-1,3-dioxolane

2-carboxymethyl-2-trifluoromethyl-4-methyl-1,3-dioxolane

Conditions
ConditionsYield
Stage #1: 2-chloro-1-propanol; methyl 3,3,3-trifluoropyruvate; 1-Chloro-2-propanol at 0℃;
Stage #2: With potassium carbonate In dimethyl sulfoxide
77%
Stage #1: 2-chloro-1-propanol; methyl 3,3,3-trifluoropyruvate; 1-Chloro-2-propanol at 0℃; for 2h;
Stage #2: With potassium carbonate In dimethyl sulfoxide for 9h;
77%
1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

sodium sulfite
7757-83-7

sodium sulfite

disodium 2-oxido-1-propanesulfonate

disodium 2-oxido-1-propanesulfonate

Conditions
ConditionsYield
In not given 180°C, 8 h;77%
In not given 180°C, 8 h;77%
tributyrin
60-01-5

tributyrin

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

(R)-1-chloro-2-propyl butyrate

(R)-1-chloro-2-propyl butyrate

Conditions
ConditionsYield
With phosphate buffer for 52h; Ambient temperature; yeast lipase catalyzed transesterification;76%
formaldehyd
50-00-0

formaldehyd

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

1-chloro-2-chloromethoxypropane
59572-29-1

1-chloro-2-chloromethoxypropane

Conditions
ConditionsYield
With hydrogenchloride at 40℃;75.6%
With hydrogenchloride
N1-BOC-N3-benzylsulfamide
147000-78-0

N1-BOC-N3-benzylsulfamide

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

N1-BOC-N3-benzyl,N3-(2-chloro-1-methylethyl) sulfamide

N1-BOC-N3-benzyl,N3-(2-chloro-1-methylethyl) sulfamide

Conditions
ConditionsYield
With di-isopropyl azodicarboxylate; triphenylphosphine In dichloromethane Alkylation;72%
tributyltin ethoxide
682-00-8

tributyltin ethoxide

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

(C4H9)3SnOCH(CH3)CH2Cl
35952-60-4

(C4H9)3SnOCH(CH3)CH2Cl

Conditions
ConditionsYield
byproducts: C2H5OH; heating of equimolar amts. of educts, removing of alc.;72%
tributyltin methoxide
1067-52-3

tributyltin methoxide

1-Chloro-2-propanol
127-00-4

1-Chloro-2-propanol

(C4H9)3SnOCH(CH3)CH2Cl
35952-60-4

(C4H9)3SnOCH(CH3)CH2Cl

Conditions
ConditionsYield
byproducts: CH3OH; heating of equimolar amts. of educts, removing of alc.;72%

1-Chloro-2-propanol Chemical Properties

Chemical Name: 1-Chloro-2-propanol
IUPAC NAME: 1-Chloropropan-2-ol ; (2S)-1-chloropropan-2-ol ; (2R)-1-chloropropan-2-ol
CAS No.: 127-00-4
EINECS: 204-819-6
RTECS: UA8942000
Molecular Formula: C3H7ClO
Molecular Weight: 94.54 g/mol
Density: 1.082 g/cm3
Flash Point: 54.5 °C
Boiling Point: 126.5 °C at 760 mmHg
Following is the structure of 1-Chloro-2-propanol (CAS No.127-00-4):


Product Categories about 1-Chloro-2-propanol (CAS No.127-00-4) is refer to Organics
The chemical synonymous of 1-Chloro-2-propanol (CAS No.127-00-4) are (±)-1-Chloro-Propan-2-Ol ; 1-Chloro-2-Hydroxypropane ; 1-Chloro-2-Propano ; 1-Chloro-2-Propanol(Sec-Propylenechlorohydrin) ; 1-Chloroisopropyl Alcohol ; 1-Chloroisopropylalcohol ; 1-Chloro-Iso-Propylalcohol,1-Propylenechloro-Hydrin ; 2-Propanol,1-Chloro-

1-Chloro-2-propanol Uses

1-Chloro-2-propanol (CAS No.127-00-4) is used as an organic synthesis intermediates,and it mainly used in the manufacture of propylene oxide and propylene glycol.

1-Chloro-2-propanol Toxicity Data With Reference

1.    

mmo-sat 40 µmol/plate

    FCTXAV    Food and Cosmetics Toxicology. 18 (1980),115.
2.    

mma-sat 1100 µg/plate

    MUREAV    Mutation Research. 30 (1975),303.
3.    

ihl-rat LC50:1000 ppm/4H

    85JCAE    Prehled Prumyslove Toxikologie; Organicke Latky Marhold, J.,Prague, Czechoslovakia.: Avicenum,1986,517.

1-Chloro-2-propanol Safety Profile

Low toxicity by inhalation. Mutation data reported. When heated to decomposition it emits toxic fumes of Cl. See also individual components.
Hazard Codes: HarmfulXn
Risk Statements about 1-Chloro-2-propanol (CAS No.127-00-4):
R10:Flammable. 
R20:Harmful by inhalation. 
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements about 1-Chloro-2-propanol (CAS No.127-00-4):
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. 
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection.
Attention:
1. Storage: Keep away from sources of ignition. Store in a cool, dry place. Store in a tightly closed container.
2. Handling: Use spark-proof tools and explosion proof equipment. Avoid breathing dust, vapor, mist, or gas. Avoid contact with skin and eyes.

1-Chloro-2-propanol Standards and Recommendations

ACGIH TLV: TWA 1 ppm (skin); Not Classifiable as a Human Carcinogen

Post buying leads

About|Contact|Cas|Product Name|Molecular|Country|Encyclopedia

Message|New Cas|MSDS|Service|Advertisement|CAS DataBase|Article Data|Manufacturers | Chemical Catalog

©2008 LookChem.com,License: ICP

NO.:Zhejiang16009103

complaints:service@lookchem.com Desktop View