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Epichlorohydrin
Cas No: 106-89-8
USD $ 3.0-3.0 / Kilogram 1 Kilogram 1-100 Metric Ton/Month Dayang Chem (Hangzhou) Co.,Ltd. Contact Supplier
Epichlorohydrin -- CHemwill
Cas No: 106-89-8
USD $ 1.0-1.0 / Metric Ton 1 Metric Ton 5 Metric Ton/Day Chemwill Asia Co., Ltd. Contact Supplier
Top purity Epichlorohydrin with high quality and best price cas:106-89-8
Cas No: 106-89-8
USD $ 50.0-100.0 / Kilogram 1 Kilogram 99999 Kilogram/Year Hangzhou Dingyan Chem Co., Ltd Contact Supplier
Epichlorohydrin
Cas No: 106-89-8
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Factory Epichlorohydrin low price CAS NO.106-89-8
Cas No: 106-89-8
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Epichlorohydrin,CAS 106-89-8
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Epichlorohydrin C3H5ClO
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Amadis Chemical offer CAS#106-89-8;CAT#A801529
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Epichlorohydrin CAS:106-89-8
Cas No: 106-89-8
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106-89-8 Usage

InChI:InChI=1/C3H5ClO/c4-1-3-2-5-3/h3H,1-2H2

106-89-8 Well-known Company Product Price

Brand (Code)Product description CAS number Packaging Price Detail
Alfa Aesar (A15823)  (±)-Epichlorohydrin, 99%    106-89-8 100g 201.0CNY Detail
Alfa Aesar (A15823)  (±)-Epichlorohydrin, 99%    106-89-8 500g 257.0CNY Detail
Alfa Aesar (A15823)  (±)-Epichlorohydrin, 99%    106-89-8 2500g 685.0CNY Detail
Sigma-Aldrich (02578)  (±)-Epichlorohydrin  analytical standard 106-89-8 02578-1ML 386.10CNY Detail
Sigma-Aldrich (45340)  (±)-Epichlorohydrin  purum, ≥99% (GC) 106-89-8 45340-500ML-F 237.51CNY Detail
Sigma-Aldrich (45340)  (±)-Epichlorohydrin  purum, ≥99% (GC) 106-89-8 45340-1L-F 601.38CNY Detail
Sigma-Aldrich (45340)  (±)-Epichlorohydrin  purum, ≥99% (GC) 106-89-8 45340-2.5L-F 1,193.40CNY Detail

106-89-8Synthetic route

3-chloroprop-1-ene
107-05-1

3-chloroprop-1-ene

epichlorohydrin
106-89-8

epichlorohydrin

Conditions
ConditionsYield
With Cumene hydroperoxide at 60 - 120℃; under 7500.75 Torr; Temperature; Pressure;99%
With Cumene hydroperoxide at 60 - 120℃; under 7500.75 Torr; Temperature; Pressure;98%
With 1-phenylethyl hydroperoxide In ethylbenzene at 30 - 50℃; under 750.075 Torr; Pressure; Temperature; Reagent/catalyst;98%
1,3-Dichloro-2-propanol
96-23-1

1,3-Dichloro-2-propanol

epichlorohydrin
106-89-8

epichlorohydrin

Conditions
ConditionsYield
With resin IRA-440 In dichloromethane for 24h; Ambient temperature;98%
With strong basic ion-exchange resin IRA 440 In dichloromethane for 24h; Product distribution; Ambient temperature; other basic ion-exchange resins; other glycerol dihalohydrins; other solvents and time;98%
With calcium hydroxide inactive form;
(C4H9)3SnOCH(CH2Cl)2
35952-61-5

(C4H9)3SnOCH(CH2Cl)2

A

tributyltin chloride
1461-22-9

tributyltin chloride

B

chloroacetone
78-95-5

chloroacetone

C

epichlorohydrin
106-89-8

epichlorohydrin

Conditions
ConditionsYield
63% decompn. at 210°C (1 h);A n/a
B 5%
C 95%
γ,γ-dichloropropanol
83682-72-8

γ,γ-dichloropropanol

epichlorohydrin
106-89-8

epichlorohydrin

Conditions
ConditionsYield
With sodium hydroxide at 20℃; Temperature;94.1%
3-chloroprop-1-ene
107-05-1

3-chloroprop-1-ene

A

1-chloro-3-methoxypropan-2-ol
4151-97-7

1-chloro-3-methoxypropan-2-ol

B

3-monochloro-1,2-propanediol
96-24-2

3-monochloro-1,2-propanediol

C

epichlorohydrin
106-89-8

epichlorohydrin

Conditions
ConditionsYield
With dihydrogen peroxide; TS-1 In methanol; water; 1,2-dichloro-benzene at 25 - 40℃; for 1h; Product distribution / selectivity;A n/a
B n/a
C 94%
2,3-Dichloro-1-propanol
616-23-9

2,3-Dichloro-1-propanol

epichlorohydrin
106-89-8

epichlorohydrin

Conditions
ConditionsYield
With water; sodium hydroxide at 50℃; for 0.00833333h; Time; Temperature; Concentration;92.4%
With potassium hydroxide
oxiranyl-methanol
556-52-5

oxiranyl-methanol

epichlorohydrin
106-89-8

epichlorohydrin

Conditions
ConditionsYield
With 1-chloro-1-(dimethylamino)-2-methyl-1-propene In dichloromethane at 0 - 20℃; Inert atmosphere;85%
1,3-Dichloro-2-propanol
96-23-1

1,3-Dichloro-2-propanol

A

chloroacetone
78-95-5

chloroacetone

B

epichlorohydrin
106-89-8

epichlorohydrin

Conditions
ConditionsYield
With HT4-c823 In water at 149.84℃; under 750.075 Torr; for 0.5h; Catalytic behavior; Reagent/catalyst; Temperature; Flow reactor; chemoselective reaction;A 18.9%
B 80.5%
(R,S)-2-hydroxy-3-chloropropyl p-toluenesulfonate
102129-99-7

(R,S)-2-hydroxy-3-chloropropyl p-toluenesulfonate

epichlorohydrin
106-89-8

epichlorohydrin

Conditions
ConditionsYield
With sodium ethane-1,2-diolate In ethylene glycol at 20℃; for 0.25h;79%
(+/-)-1-Acetoxy-2,3-dichloropropane
589-96-8

(+/-)-1-Acetoxy-2,3-dichloropropane

epichlorohydrin
106-89-8

epichlorohydrin

Conditions
ConditionsYield
With calcium hydroxide 1.) H2O, r.t., 1 h, 2.) hexane, 6 h;77%
glycerol
56-81-5

glycerol

epichlorohydrin
106-89-8

epichlorohydrin

Conditions
ConditionsYield
Stage #1: glycerol With hydrogenchloride; Adipic acid In water at 120℃; for 8h;
Stage #2: With calcium hydroxide
67.5%
With phosphorus trichloride
With hydrogenchloride anschl. mit Aetzkali;
1-bromo-3-chloro-propan-2-ol
4540-44-7

1-bromo-3-chloro-propan-2-ol

epichlorohydrin
106-89-8

epichlorohydrin

Conditions
ConditionsYield
With sodium ethane-1,2-diolate In ethylene glycol at 20℃; for 0.25h;58%
With potassium hydroxide levorotatory form;
2,3-Dichloro-1-propanol
616-23-9

2,3-Dichloro-1-propanol

A

(2R)-3-chloro-1,2-propanediol
57090-45-6

(2R)-3-chloro-1,2-propanediol

B

(S)-3-chloropropan-1,2-diol
60827-45-4

(S)-3-chloropropan-1,2-diol

C

(S)-1,3-dichloro-1-propanol

(S)-1,3-dichloro-1-propanol

D

epichlorohydrin
106-89-8

epichlorohydrin

Conditions
ConditionsYield
With epoxide hydrolase from Agrobacterium radiobacter AD1; halohydrin dehalogenase from Agrobacterium radiobacter AD1; Tris-SO4 buffer In water at 30℃; for 20h; pH=7.5; kinetic resolution; Further byproducts given;A n/a
B n/a
C 49.5%
D n/a
dihydrogen peroxide
7722-84-1

dihydrogen peroxide

3-chloroprop-1-ene
107-05-1

3-chloroprop-1-ene

A

water
7732-18-5

water

B

epichlorohydrin
106-89-8

epichlorohydrin

Conditions
ConditionsYield
With titanium-containing zeolite In methanol at 35℃; Mechanism; Solvent;A n/a
B 29.8%
3-chloroprop-1-ene
107-05-1

3-chloroprop-1-ene

A

benzaldehyde
100-52-7

benzaldehyde

B

epichlorohydrin
106-89-8

epichlorohydrin

Conditions
ConditionsYield
With molybdenum blue; dihydrogen peroxide; bis(tri-n-butyltin)oxide In chloroform at 25℃; for 10h;A 1%
B 48 % Turnov.
1,3-Dichloro-2-propanol
96-23-1

1,3-Dichloro-2-propanol

A

glycerol
56-81-5

glycerol

B

epichlorohydrin
106-89-8

epichlorohydrin

Conditions
ConditionsYield
With potassium hydroxide
1,3-dichloro-2-acetoxypropane
3674-10-0

1,3-dichloro-2-acetoxypropane

A

acetyl chloride
75-36-5

acetyl chloride

B

epichlorohydrin
106-89-8

epichlorohydrin

Conditions
ConditionsYield
beim Stehenlassen;
peracetic acid
79-21-0

peracetic acid

3-chloroprop-1-ene
107-05-1

3-chloroprop-1-ene

epichlorohydrin
106-89-8

epichlorohydrin

Conditions
ConditionsYield
With catalysts
(+-)-2,3-dichloro-propan-1-ol

(+-)-2,3-dichloro-propan-1-ol

epichlorohydrin
106-89-8

epichlorohydrin

Conditions
ConditionsYield
With calcium hydroxide
With sodium hydroxide Herstellung eines mit Chlor-36 markierten Praeparats;
1-bromo-3-chloro-propan-2-ol
4540-44-7

1-bromo-3-chloro-propan-2-ol

potash

potash

A

hydrogen bromide
10035-10-6, 12258-64-9

hydrogen bromide

B

epichlorohydrin
106-89-8

epichlorohydrin

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

1,3-Dichloro-2-propanol

KOH

KOH

epichlorohydrin
106-89-8

epichlorohydrin

2,3-Dichloro-1-propanol
616-23-9

2,3-Dichloro-1-propanol

potash

potash

epichlorohydrin
106-89-8

epichlorohydrin

2,3-Dichloro-1-propanol
616-23-9

2,3-Dichloro-1-propanol

water
7732-18-5

water

sodium hydroxide

sodium hydroxide

epichlorohydrin
106-89-8

epichlorohydrin

Conditions
ConditionsYield
at 0℃;
at 0℃; Geschwindigkeit;
at 25℃; Geschwindigkeit;
1-chloro-3-iodopropan-2-ol
26484-95-7

1-chloro-3-iodopropan-2-ol

KOH-solution

KOH-solution

A

hydrogen iodide
10034-85-2

hydrogen iodide

B

epichlorohydrin
106-89-8

epichlorohydrin

diethyl ether
60-29-7

diethyl ether

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

1,3-Dichloro-2-propanol

water
7732-18-5

water

sodium amalgam

sodium amalgam

A

allyl alcohol
107-18-6

allyl alcohol

B

epichlorohydrin
106-89-8

epichlorohydrin

diethyl ether
60-29-7

diethyl ether

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

1,3-Dichloro-2-propanol

sodium

sodium

A

propene
187737-37-7

propene

B

allyl alcohol
107-18-6

allyl alcohol

C

epichlorohydrin
106-89-8

epichlorohydrin

ethanol
64-17-5

ethanol

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

1,3-Dichloro-2-propanol

powdered NaOH

powdered NaOH

A

1,3-diethoxy-isopropanol
4043-59-8

1,3-diethoxy-isopropanol

B

epichlorohydrin
106-89-8

epichlorohydrin

C

glycidethyl ether

glycidethyl ether

3-hydroxy-benzoic acid-(2-chloro-1-chloromethyl-ethyl ester)

3-hydroxy-benzoic acid-(2-chloro-1-chloromethyl-ethyl ester)

potash

potash

epichlorohydrin
106-89-8

epichlorohydrin

Conditions
ConditionsYield
at 100℃;
morpholine
110-91-8

morpholine

epichlorohydrin
106-89-8

epichlorohydrin

1-chloro-3-(4-morpholinyl)-2-propanol
40893-69-4

1-chloro-3-(4-morpholinyl)-2-propanol

Conditions
ConditionsYield
In ethanol for 24h; Heating;100%
With zinc(II) chloride In water at 60℃; for 8h; regioselective reaction;96%
In water at 0 - 5℃; for 4h;92%
Ethyl 4-hydroxybenzoate
120-47-8

Ethyl 4-hydroxybenzoate

epichlorohydrin
106-89-8

epichlorohydrin

ethyl 4-(glycidyloxy)benzoate
50625-94-0

ethyl 4-(glycidyloxy)benzoate

Conditions
ConditionsYield
With sodium carbonate; N,N-dimethyl-formamide at 80℃; for 12h; Inert atmosphere;100%
With potassium carbonate In acetone for 20h; Heating;
With potassium carbonate In butanone Heating;
With potassium carbonate In acetone; toluene13.5 gm (61%)
With sodium hydroxide
acetic acid
64-19-7

acetic acid

epichlorohydrin
106-89-8

epichlorohydrin

3-chloro-2-hydroxy-1-propyl acetate
24573-30-6

3-chloro-2-hydroxy-1-propyl acetate

Conditions
ConditionsYield
With iron(III) chloride at 20 - 70℃; for 24.1667h;100%
With tin(IV)tetraphenylporphyrinato trifluoromethanesulfonate for 0.666667h; Heating;99%
With cerium(IV) triflate at 80℃; for 0.0833333h;93%
epichlorohydrin
106-89-8

epichlorohydrin

phenol
108-95-2

phenol

Phenyl glycidyl ether
122-60-1

Phenyl glycidyl ether

Conditions
ConditionsYield
Stage #1: phenol With sodium hydroxide In water at 25℃; for 0.666667h;
Stage #2: epichlorohydrin In water at 30 - 35℃; for 16h;
100%
With n-Bu4NOSO2OCH2CHOHCH3; potassium carbonate at 75 - 80℃; for 1.5h;91%
With n-BuNOSO2OCH2CHOHCH3; potassium carbonate at 75 - 80℃; for 1.5h; other aryl alcohols, var. phase transfer catalysts, var. reaction time;91%
epichlorohydrin
106-89-8

epichlorohydrin

1-bromo-3-chloro-propan-2-ol
4540-44-7

1-bromo-3-chloro-propan-2-ol

Conditions
ConditionsYield
With hydrogen bromide at -60℃; for 16h;100%
With dimethylbromosulphonium bromide In acetonitrile at 20℃; for 0.333333h;98%
With ammonium cerium(IV) nitrate; tetrabutylammomium bromide In tert-butyl alcohol for 1.5h; Ambient temperature;96%
epichlorohydrin
106-89-8

epichlorohydrin

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

1,3-Dichloro-2-propanol

Conditions
ConditionsYield
With hydrogenchloride In dichloromethane for 12h; Ambient temperature;100%
With hydrogenchloride In water100%
With chloro-trimethyl-silane; 3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate at 20℃; for 1h; ring opening reaction;99%
epichlorohydrin
106-89-8

epichlorohydrin

bis(3-chloro-2-hydroxypropyl)sulfide
19030-86-5

bis(3-chloro-2-hydroxypropyl)sulfide

Conditions
ConditionsYield
With hydrogenchloride; sodium hydrogen sulfide monohydrate; sodium hydroxide In methanol; water at 6℃;100%
With hydrogen sulfide; tetrabutylammomium bromide In toluene at 20 - 25℃; Solvent; Temperature; Reagent/catalyst;96%
With hydrogen sulfide
diisopropylamine
108-18-9

diisopropylamine

epichlorohydrin
106-89-8

epichlorohydrin

1-Chlor-2-hydroxy-3-diisopropylamino-methyl-propan
55211-97-7

1-Chlor-2-hydroxy-3-diisopropylamino-methyl-propan

Conditions
ConditionsYield
In ethanol for 24h; Heating;100%
In water
aniline
62-53-3

aniline

epichlorohydrin
106-89-8

epichlorohydrin

N-(3-chloro-2-hydroxypropyl)aniline
76226-32-9, 15949-12-9

N-(3-chloro-2-hydroxypropyl)aniline

Conditions
ConditionsYield
With lithium bromide at 20℃; for 5h;100%
With Ni2+-metallodendrimer grafted on mesoporous polymethacrylate based Sepabeads EB-EP-400 In neat (no solvent) at 20℃; for 0.5h; Reagent/catalyst; Solvent; Green chemistry; regioselective reaction;97%
With BiCl6(3-)*2C4H10N2*ClH*3H(1+)*H2O at 20℃; for 0.116667h; Neat (no solvent); regioselective reaction;96%
pyrrolidine
123-75-1

pyrrolidine

epichlorohydrin
106-89-8

epichlorohydrin

1-chloro-3-(1-pyrrolidinyl)-2-propanol
58759-70-9

1-chloro-3-(1-pyrrolidinyl)-2-propanol

Conditions
ConditionsYield
In ethanol for 24h; Heating;100%
In ethanol at 20℃; under 2585.81 Torr; for 0.0166667h; microwave irradiation;65%
(2-hydroxyethyl)(methyl)amine
109-83-1

(2-hydroxyethyl)(methyl)amine

epichlorohydrin
106-89-8

epichlorohydrin

1-Chlor-2-hydroxy-3-(N-methyl-N-2-hydroxyethyl)-amino-propan
63125-83-7

1-Chlor-2-hydroxy-3-(N-methyl-N-2-hydroxyethyl)-amino-propan

Conditions
ConditionsYield
at 40 - 70℃;100%
In water at 13 - 34℃; for 1.41667h;
In isopropyl alcohol
1H-indol-4-ol
2380-94-1

1H-indol-4-ol

epichlorohydrin
106-89-8

epichlorohydrin

4-(oxiranylmethoxy)-1H-indole
35308-87-3

4-(oxiranylmethoxy)-1H-indole

Conditions
ConditionsYield
With potassium hydroxide In dimethyl sulfoxide at 45℃; for 4h;100%
Stage #1: 1H-indol-4-ol; epichlorohydrin With potassium hydroxide In dimethyl sulfoxide at 45℃; for 4h;
Stage #2: With ammonium chloride In water
99%
With potassium hydroxide In dimethyl sulfoxide at 45℃; for 4h;99%
4-phenyl-Δ2-1,2,4-triazoline-5-thione
5373-72-8

4-phenyl-Δ2-1,2,4-triazoline-5-thione

epichlorohydrin
106-89-8

epichlorohydrin

4-phenyl-3-(1-chloro-2-hydroxypropylthio)-1,2,4-triazole
134619-57-1

4-phenyl-3-(1-chloro-2-hydroxypropylthio)-1,2,4-triazole

Conditions
ConditionsYield
In ethanol at 20℃; for 5h;100%
1-octadecanol
112-92-5

1-octadecanol

epichlorohydrin
106-89-8

epichlorohydrin

octadecyl glycidyl ether
16245-97-9

octadecyl glycidyl ether

Conditions
ConditionsYield
With sodium hydroxide; Aliquat 336 In cyclohexane Heating;100%
With sodium hydroxide; Aliquat 336 In cyclohexane Heating;99%
With sodium hydroxide; Aliquat 336 In cyclohexane for 4h; Heating;99%
trimethylsilyl cyanide
7677-24-9

trimethylsilyl cyanide

epichlorohydrin
106-89-8

epichlorohydrin

4-chloro-3-trimethylsiloxybutyronitrile
81091-27-2

4-chloro-3-trimethylsiloxybutyronitrile

Conditions
ConditionsYield
With erbium(III) triflate at 0 - 20℃; for 0.166667h; regioselective reaction;100%
ytterbium cyanide In tetrahydrofuran at 25℃; for 0.3h;91%
carbon dioxide
124-38-9

carbon dioxide

epichlorohydrin
106-89-8

epichlorohydrin

4-chloromethyl-[1,3]dioxolan-2-one
2463-45-8

4-chloromethyl-[1,3]dioxolan-2-one

Conditions
ConditionsYield
With dmap; CrTTPCl at 60℃; under 37751.8 - 40337.5 Torr; for 18h;100%
With triphenylphosphine; phenol at 120℃; under 30002.4 Torr; for 14h;100%
With triethylamine; binaphthyldiamino Zn(II) salen-type compex In dichloromethane at 100℃; under 25858.1 Torr;100%
Cyclododecylamine
1502-03-0

Cyclododecylamine

epichlorohydrin
106-89-8

epichlorohydrin

1-Chloro-3-cyclododecylamino-propan-2-ol

1-Chloro-3-cyclododecylamino-propan-2-ol

Conditions
ConditionsYield
In ethanol for 24h; Heating;100%
isoselenocyanatotrimethylsilane
16966-40-8

isoselenocyanatotrimethylsilane

epichlorohydrin
106-89-8

epichlorohydrin

3-Chloro-2-trimethylsiloxypropyl selenocyanate
128256-05-3

3-Chloro-2-trimethylsiloxypropyl selenocyanate

Conditions
ConditionsYield
potassium selenocyanate In hexane at 40℃; for 24h;100%
cyclooctylamine
5452-37-9

cyclooctylamine

epichlorohydrin
106-89-8

epichlorohydrin

1-Chloro-3-cyclooctylamino-propan-2-ol

1-Chloro-3-cyclooctylamino-propan-2-ol

Conditions
ConditionsYield
In ethanol for 24h; Heating;100%
pyridinium perchlorate
15598-34-2

pyridinium perchlorate

epichlorohydrin
106-89-8

epichlorohydrin

1-(2-hydroxy-3-chloropropyl)pyridinium perchlorate

1-(2-hydroxy-3-chloropropyl)pyridinium perchlorate

Conditions
ConditionsYield
With pyridine In ethanol for 3h; Product distribution; Heating; further cycloimmonium salts;100%
With pyridine In ethanol for 3h; Heating;100%
4-methylpyridinium perchlorate
52827-74-4

4-methylpyridinium perchlorate

epichlorohydrin
106-89-8

epichlorohydrin

1-(2-hydroxy-3-chloropropyl)-4-methylpyridinium perchlorate

1-(2-hydroxy-3-chloropropyl)-4-methylpyridinium perchlorate

Conditions
ConditionsYield
With picoline for 1h; Heating;100%
cinnamoyl chloride
102-92-1

cinnamoyl chloride

epichlorohydrin
106-89-8

epichlorohydrin

1,3-dichloro-2-propyl cinnamate
157140-94-8

1,3-dichloro-2-propyl cinnamate

Conditions
ConditionsYield
With yttrium(III) chloride In dichloromethane for 36h; Ambient temperature;100%
N-(1-chlorohexafluoro-1-methylethyl)benzenesulfinimidoyl chloride
85095-40-5

N-(1-chlorohexafluoro-1-methylethyl)benzenesulfinimidoyl chloride

epichlorohydrin
106-89-8

epichlorohydrin

C12H10Cl3F6NOS
91363-16-5

C12H10Cl3F6NOS

Conditions
ConditionsYield
In tetrachloromethane at 25℃; for 48h;100%
N-(2-chlorohexafluoroisopropyl)-p-toluenesulfinimidoyl chloride
85095-41-6

N-(2-chlorohexafluoroisopropyl)-p-toluenesulfinimidoyl chloride

epichlorohydrin
106-89-8

epichlorohydrin

C13H12Cl3F6NOS
91363-17-6

C13H12Cl3F6NOS

Conditions
ConditionsYield
In tetrachloromethane at 25℃; for 48h;100%
N-cyclohexyl-cyclohexanamine
101-83-7

N-cyclohexyl-cyclohexanamine

epichlorohydrin
106-89-8

epichlorohydrin

1-Chloro-3-dicyclohexylamino-propan-2-ol
150389-77-8

1-Chloro-3-dicyclohexylamino-propan-2-ol

Conditions
ConditionsYield
In ethanol for 24h; Heating;100%
(2-trimethylsilylprop-2-en-1-yl)tributylstannane
151073-99-3

(2-trimethylsilylprop-2-en-1-yl)tributylstannane

epichlorohydrin
106-89-8

epichlorohydrin

1-Chloro-5-(trimethylsilyl)-5-hexen-2-ol

1-Chloro-5-(trimethylsilyl)-5-hexen-2-ol

Conditions
ConditionsYield
With ethylaluminum dichloride In dichloromethane at -78℃; for 19h;100%
2-Allylphenol
1745-81-9

2-Allylphenol

epichlorohydrin
106-89-8

epichlorohydrin

1-(2-allyl-phenoxy)-3-chloro-propan-2-ol
49716-04-3

1-(2-allyl-phenoxy)-3-chloro-propan-2-ol

Conditions
ConditionsYield
With pyridine In chloroform; water; phenol100%
With piperidine Heating;
epichlorohydrin
106-89-8

epichlorohydrin

p-cyclohexylphenol
1131-60-8

p-cyclohexylphenol

2-[(4-cyclohexylphenoxy)methyl]oxirane
67006-99-9

2-[(4-cyclohexylphenoxy)methyl]oxirane

Conditions
ConditionsYield
With sodium hydroxide for 1h; Reflux;100%
With sodium In isopropyl alcohol 1.) 10 min., reflux, 2.) 16 h., room temp.;
epichlorohydrin
106-89-8

epichlorohydrin

bis(2-bromo-2-chloropropyl)(2-bromo-3-chloropropyl)phosphonate
36636-44-9

bis(2-bromo-2-chloropropyl)(2-bromo-3-chloropropyl)phosphonate

Conditions
ConditionsYield
With phosphorus tribromide at 0 - 40℃;100%
epichlorohydrin
106-89-8

epichlorohydrin

phenol
108-95-2

phenol

(R)-1-chloro-3-phenoxy-2-propanol
140630-45-1

(R)-1-chloro-3-phenoxy-2-propanol

Conditions
ConditionsYield
With chiral oligo-(salen)Co(OTs) complexes; lutidinium p-toluene sulfonate In acetonitrile at 4℃; for 4h;100%
With (R,R)-(salen)Co(H2O); 3 A molecular sieve In various solvent(s) at -15℃;97%
With C57H68N4O8(2-)*Co(3+)*C7H7O3S(1-); C56H66N2O6(2-)*Co(3+)*C7H7O3S(1-) In tetrachloromethane at 4 - 20℃; for 6h; stereoselective reaction;95%
With Co(salen) macrocycles 1(OTs) In tert-butyl methyl ether at 20℃; for 9h; optical yield given as %ee; enantioselective reaction;91%
With Co(salen) macrocycles 1(OTs) In tert-butyl methyl ether at 20℃; Kinetics; enantioselective reaction;
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