methyloxirane
1-Chloro-2-propanol
Conditions | Yield |
---|---|
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
A
2-chloro-1-propanol
B
allyl alcohol
C
1-Chloro-2-propanol
Conditions | Yield |
---|---|
With hydrogenchloride In solid at 60 - 70℃; for 7h; in tri-o-thymotide clathrate; | A 5% B 87% C 8% |
Conditions | Yield |
---|---|
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% |
Conditions | Yield |
---|---|
With chlorourea; acetic acid | A n/a B 80% |
With hypochloric acid | |
With sulfuric acid; chloroamine-T In water; acetone at 50℃; Yield given. Yields of byproduct given; |
Conditions | Yield |
---|---|
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
1-Chloro-2-propanol
Conditions | Yield |
---|---|
With lithium chloride In tetrachloromethane; acetone for 1h; | 80% |
Conditions | Yield |
---|---|
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
methyloxirane
A
1-methoxy-2-propanol
B
2-methoxypropanol
C
1-Chloro-2-propanol
Conditions | Yield |
---|---|
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
A
1-chloro-2-acetoxypropane
C
toluene-4-sulfonamide
D
1-Chloro-2-propanol
Conditions | Yield |
---|---|
With chloroamine-T; acetic acid at 50 - 60℃; for 3h; | A 43% B 17% C n/a D 10% E n/a |
propene
acetic acid
A
1-chloro-2-acetoxypropane
C
toluene-4-sulfonamide
D
1-Chloro-2-propanol
Conditions | Yield |
---|---|
With chloroamine-T at 50 - 60℃; for 3h; | A 43% B 17% C n/a D 10% E n/a |
propene
chloramine T trihydrate
A
1-chloro-2-acetoxypropane
C
toluene-4-sulfonamide
D
1-Chloro-2-propanol
Conditions | Yield |
---|---|
With acetic acid at 50 - 60℃; for 3h; | A 43% B 17% C n/a D 10% E n/a |
Conditions | Yield |
---|---|
With hydrogenchloride | |
With tetrachlorosilane | |
With sulphur monochloride |
Conditions | Yield |
---|---|
With water at 18 - 42℃; |
propene
1-Chloro-2-propanol
Conditions | Yield |
---|---|
With water; chlorine | |
With water; chlorine; copper dichloride | |
With hypochloric acid |
Conditions | Yield |
---|---|
With cis-nitrous acid |
Conditions | Yield |
---|---|
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; |
Conditions | Yield |
---|---|
With cis-nitrous acid |
Conditions | Yield |
---|---|
With 2,4,6-trimethyl-pyridine; 8-quinolinylboronic acid In N,N-dimethyl-formamide |
propylene glycol
A
2-chloro-1-propanol
B
1-Chloro-2-propanol
C
methyloxirane
Conditions | Yield |
---|---|
With tert-butylhypochlorite; potassium carbonate; triphenylphosphine In chloroform Product distribution; 1.) -70 deg C, 2.) RT, 3.) reflux, 24 h; |
propene
A
1,2-Dichloropropane
B
bis(3-chloropropyl)ether
C
bis(1-chloro-2-propyl) ether
D
1-Chloro-2-propanol
Conditions | Yield |
---|---|
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
A
propan-1-ol
B
1,2-Dichloropropane
D
1-Chloro-2-propanol
Conditions | Yield |
---|---|
at 180℃; Rate constant; Mechanism; Product distribution; |
1-(p-cyanophenyl)3-(2-chloropropyl)triazene
A
2-chloropropene
B
2-chloro-1-propanol
C
1,2-Dichloropropane
D
acetone
E
1-Chloro-2-propanol
F
4-Aminobenzonitrile
Conditions | Yield |
---|---|
In water; acetonitrile at 37.5℃; decomposition half-life; pH=7.1; |
3-chloroprop-1-ene
A
allyl alcohol
B
1-Chloro-2-propanol
C
methyloxirane
Conditions | Yield |
---|---|
With sodium tetrahydroborate; mercury(II) diacetate Product distribution; 2.) EtOH; | A 3 % Chromat. B 70 % Chromat. C 21 % Chromat. |
chloro-trimethyl-silane
methyloxirane
A
2-chloro-1-propanol
B
1-Chloro-2-propanol
Conditions | Yield |
---|---|
With cesium fluoride 1) CH2Cl2, r.t., 2) MeOH, r.t., 1 h; Multistep reaction. Title compound not separated from byproducts; |
Conditions | Yield |
---|---|
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
A
1,3-Dichloro-2-propanol
B
bis-(4-chlorobutyl)ether
C
1-Chloro-2-propanol
Conditions | Yield |
---|---|
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; |
Conditions | Yield |
---|---|
inactive form; |
hydrogenchloride
diethyl ether
methyloxirane
A
2-chloro-1-propanol
B
1-Chloro-2-propanol
Conditions | Yield |
---|---|
at -55 - 35℃; |
hydrogenchloride
water
methyloxirane
A
2-chloro-1-propanol
B
1-Chloro-2-propanol
Conditions | Yield |
---|---|
at 15 - 83℃; |
boron trichloride
methyloxirane
A
2-chloro-1-propanol
B
1-Chloro-2-propanol
Conditions | Yield |
---|---|
anschliessend mit Methanol; |
chloro-diphenylphosphine
1-Chloro-2-propanol
(2-chloro-1-methylethoxy)diphenylphosphane
Conditions | Yield |
---|---|
With triethylamine In diethyl ether at 0℃; for 0.5h; | 98% |
4-Phenoxyphenol
1-Chloro-2-propanol
(R,S)-2-hydroxypropyl 4-phenoxyphenyl ether
Conditions | Yield |
---|---|
With sodium hydroxide In water; toluene at 85℃; for 0.166667h; Temperature; Reagent/catalyst; | 95% |
2-nitrothiophenol
1-Chloro-2-propanol
B
1-(2-nitro-phenylsulfanyl)-propan-2-ol
Conditions | Yield |
---|---|
With sodium hydroxide In water | A n/a B 94.8% |
diphenyl(methyl)phosphine
1-Chloro-2-propanol
(2-Hydroxypropyl)(methyl)diphenylphosphonium-chlorid
Conditions | Yield |
---|---|
In acetonitrile at 75 - 80℃; for 96h; | 94% |
Conditions | Yield |
---|---|
With sodium hydroxide for 0.0208333h; microwave irradiation; | 94% |
With pyridine Acetylation; |
Conditions | Yield |
---|---|
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)
carbon monoxide
1-Chloro-2-propanol
Conditions | Yield |
---|---|
With dipotassium peroxodisulfate In dichloromethane at 20℃; under 760.051 Torr; Darkness; | 91% |
1,2,5,6-tetrahydrobenzoic acid
1-Chloro-2-propanol
Cyclohex-3-enecarboxylic acid 2-chloro-1-methyl-ethyl ester
Conditions | Yield |
---|---|
With sulfuric acid In toluene at 130℃; | 90% |
With sulfuric acid In toluene at 90℃; Rate constant; |
2-methyl-1,4-naphthohydroquinone
1-Chloro-2-propanol
4-(1-Chlor-2-propoxy)-2-methyl-1-naphthol
Conditions | Yield |
---|---|
With hydrogenchloride at 60℃; for 0.75h; | 88% |
4-methyleneoxetan-2-one
1-Chloro-2-propanol
3-Oxo-butyric acid 2-chloro-1-methyl-ethyl ester
Conditions | Yield |
---|---|
at 100 - 120℃; for 4.08333h; | 86% |
Conditions | Yield |
---|---|
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% |
Conditions | Yield |
---|---|
With sodium hydroxide In ethanol 1.) heating, 30 min, 2.) reflux; | 85% |
4-phenylisoquinolin-1(2H)-one
1-Chloro-2-propanol
2-(2-hydroxypropyl)-4-phenyl-1(2H)-isoquinolone
Conditions | Yield |
---|---|
With potassium carbonate In N-methyl-acetamide | 81% |
4-chlorophenylethylamine
1-Chloro-2-propanol
1-[[2-(4-chlorophenyl)ethyl]amino]-2-hydroxypropane
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 20 - 60℃; Reagent/catalyst; Inert atmosphere; | 80.1% |
2,4-dibromophenol
1-Chloro-2-propanol
(+/-)-1-(2,4-dibromophenoxy)-2-propanol
Conditions | Yield |
---|---|
With sodium hydroxide In water for 24h; Reflux; | 80% |
Conditions | Yield |
---|---|
In pyridine at 20℃; for 2h; | 79% |
at 170℃; |
Northiadene
1-Chloro-2-propanol
(E)-11-(3-propylidene)-6,11-dihydrodibenzothiepin
Conditions | Yield |
---|---|
With sodium carbonate In N,N-dimethyl-formamide | 77% |
Conditions | Yield |
---|---|
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% |
Conditions | Yield |
---|---|
In not given 180°C, 8 h; | 77% |
In not given 180°C, 8 h; | 77% |
Conditions | Yield |
---|---|
With phosphate buffer for 52h; Ambient temperature; yeast lipase catalyzed transesterification; | 76% |
Conditions | Yield |
---|---|
With hydrogenchloride at 40℃; | 75.6% |
With hydrogenchloride |
N1-BOC-N3-benzylsulfamide
1-Chloro-2-propanol
Conditions | Yield |
---|---|
With di-isopropyl azodicarboxylate; triphenylphosphine In dichloromethane Alkylation; | 72% |
Conditions | Yield |
---|---|
byproducts: C2H5OH; heating of equimolar amts. of educts, removing of alc.; | 72% |
Conditions | Yield |
---|---|
byproducts: CH3OH; heating of equimolar amts. of educts, removing of alc.; | 72% |
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 (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. | 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. |
Low toxicity by inhalation. Mutation data reported. When heated to decomposition it emits toxic fumes of Cl−. See also individual components.
Hazard Codes: Xn
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.
ACGIH TLV: TWA 1 ppm (skin); Not Classifiable as a Human Carcinogen
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