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105-64-6

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105-64-6 Usage

Chemical Properties

White crystalline solid with a mild characteristicodor; mp 8–10°C (46.4–50°F); density1.080 at 15°C (59°F); slightly soluble inwater, 0.04% at 25°C (77°F), soluble in ether,chloroform, benzene, hexane, and isooctane.

Uses

It is used as a catalyst to initiate polymerizationreactions to produce polymers fromethylene, styrene, vinyl acetate, vinyl chloride,and vinyl esters. Polymers of increasedlinearity and better properties can be obtainedby optimizing its concentration, temperature,and pressure conditions.

Synthesis Reference(s)

Journal of the American Chemical Society, 72, p. 1254, 1950 DOI: 10.1021/ja01159a052

General Description

A white solid (shipped packed in Dry Ice to stabilize) with a sharp unpleasant odor. Insoluble in sater and sinks in water. Used as polymerization catalyst.

Air & Water Reactions

Highly flammable. Insoluble in water. Spontaneous decomposition at room temperature releases flammable toxic products.

Reactivity Profile

ISOPROPYL PEROXYDICARBONATE decomposes violently or explosively at temperatures 0-10°C owing to self- accelerating exothermic decomposition; Several explosions were due to shock, heat, or friction; amines and certain metals can cause accelerated decomposition [Bretherick 1979 p. 156]. Spontaneous decomposition possible at room temperature to release flammable and corrosive products (presence of stabilizer reduces this possibility). A strong oxidizing agent. May ignite organic compounds on contact, hence a fire risk. Strongly reduced material such as sulfides, nitrides, and hydrides can react explosively. Reacts at least to produce heat when mixed with members of most chemical classes. These reactions often generate gases (toxic and nontoxic). Subject to decomposition, buildup of heat and even an explosion if contaminated with a catalyst (often a transition metal such as cobalt, iron, manganese, nickel, or vanadium or a salt of a transition metal).

Health Hazard

Different sources of media describe the Health Hazard of 105-64-6 differently. You can refer to the following data:
1. Inhalation overexposure unlikely, but prolonged exposure may cause lung edema. Contact with eyes may cause irritation. Solutions are severe primary skin irritants.
2. Diisopropyl peroxydicarbonate is a moderateskin irritant. The irritation can be severe onrabbit skin. Eye contact can cause conjunctivitisand corneal ulcerations, which, however,are fully recoverable in 1–2 weeks. Itstoxicity is very low. There is no report of itsill effect on humans. It may cause dermatitison sensitive skin.LD50 value, oral (rats): 21,410 mg/kg.

Chemical Reactivity

Reactivity with Water No reaction; Reactivity with Common Materials: May decompose with the formation of oxygen when in contact with metals; Stability During Transport: Unstable at temperatures above 0°F with the formation of oxygen gas; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent.

Safety Profile

Moderately toxic by ingestion and skin contact. A severe eye irritant. Very dangerous fire hazard. Dangerously unstable above 10°C. An impactand heat-sensitive explosive. Solutions may spontaneously explode (the hazard increases with concentration). Storage in sealed containers map be dangerous. Explodes on contact with amines or potassium iodide. May explode on contact with organic matter. When heated to decomposition it emits acrid smoke and fumes. See also PEROXIDES, ORGANIC

Waste Disposal

Larger quantities can be disposed of by scatteringin a disposal area where it melts andgradually decomposes. Small quantities aredestroyed by adding slowly to 5% alcoholicKOH. Solutions in small amount may be disposedof in porous sandy soils.

Check Digit Verification of cas no

The CAS Registry Mumber 105-64-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 105-64:
(5*1)+(4*0)+(3*5)+(2*6)+(1*4)=36
36 % 10 = 6
So 105-64-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O4/c1-5(2)9-7(8)11-10-6(3)4/h5-6H,1-4H3

105-64-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name propan-2-yl propan-2-yloxycarbonyloxy carbonate

1.2 Other means of identification

Product number -
Other names Bisisopropyl peroxydicarbonate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:105-64-6 SDS

105-64-6Synthetic route

isopropyl chloroformate
108-23-6

isopropyl chloroformate

diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

Conditions
ConditionsYield
With sodium hydroxide; dihydrogen peroxide99%
With sodium hydroxide; dihydrogen peroxide In water at 15℃; Product distribution / selectivity;94%
With dihydrogen peroxide; potassium hydroxide In water at 5 - 50℃; for 0.0766667h; Flow reactor;74.7%
With sodium peroxide
With sodium hydroxide; dihydrogen peroxide
2,2,6,6-Tetramethyl-1-piperidinyloxy free radical
2564-83-2, 45842-10-2

2,2,6,6-Tetramethyl-1-piperidinyloxy free radical

diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

1,4-Divinylbenzene
105-06-6

1,4-Divinylbenzene

2-(isopropyloxycarbonyloxy)-1-(2',2',6',6'-tetramethyl-1'-piperidinyloxy)-1-(4'-vinylphenyl)ethane
262616-04-6

2-(isopropyloxycarbonyloxy)-1-(2',2',6',6'-tetramethyl-1'-piperidinyloxy)-1-(4'-vinylphenyl)ethane

Conditions
ConditionsYield
at 55℃; for 5h;76.1%
4-acetoxy-2,2,6,6-tetramethylpiperidine-1-oxyl
132969-46-1

4-acetoxy-2,2,6,6-tetramethylpiperidine-1-oxyl

diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

1,4-Divinylbenzene
105-06-6

1,4-Divinylbenzene

2-(isopropyloxycarbonyloxy)-1-(4'-acetoxy-2',2',6',6'-tetramethyl-1'-piperidinyloxy)-1-(4'-vinylphenyl)ethane

2-(isopropyloxycarbonyloxy)-1-(4'-acetoxy-2',2',6',6'-tetramethyl-1'-piperidinyloxy)-1-(4'-vinylphenyl)ethane

Conditions
ConditionsYield
at 0 - 55℃; for 5h;73%
2,2,6,6-Tetramethyl-1-piperidinyloxy free radical
2564-83-2, 45842-10-2

2,2,6,6-Tetramethyl-1-piperidinyloxy free radical

diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

1,3-divinylbenzene
108-57-6

1,3-divinylbenzene

2-(isopropyloxycarbonyloxy)-1-(2',2',6',6'-tetramethyl-1'-piperidinyloxy)-1-(3'-vinylphenyl)ethane

2-(isopropyloxycarbonyloxy)-1-(2',2',6',6'-tetramethyl-1'-piperidinyloxy)-1-(3'-vinylphenyl)ethane

Conditions
ConditionsYield
70.5%
4-(benzyloxycarbonyl)-2,2,6,6-tetramethylpiperidine-1-oxyl
3225-26-1

4-(benzyloxycarbonyl)-2,2,6,6-tetramethylpiperidine-1-oxyl

diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

1,4-Divinylbenzene
105-06-6

1,4-Divinylbenzene

2-(isopropyloxycarbonyloxy)-1-(4'-benzoyloxy-2',2',6',6'-tetramethyl-1'-piperidinyloxy)-1-(4'-vinylphenyl)ethane

2-(isopropyloxycarbonyloxy)-1-(4'-benzoyloxy-2',2',6',6'-tetramethyl-1'-piperidinyloxy)-1-(4'-vinylphenyl)ethane

Conditions
ConditionsYield
at 0 - 55℃; for 5h;62.1%
diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

N-(4-chlorophenylmethylene)-2-methylthiobenzenamine
142505-38-2

N-(4-chlorophenylmethylene)-2-methylthiobenzenamine

A

2-(4-chlorophenyl)benzothiazole
6265-91-4

2-(4-chlorophenyl)benzothiazole

B

4-chlorobenzaldehyde
104-88-1

4-chlorobenzaldehyde

C

(2-aminophenyl)thiomethyl isopropyl carbonate
142505-43-9

(2-aminophenyl)thiomethyl isopropyl carbonate

Conditions
ConditionsYield
In benzene at 60℃; for 5h;A 36%
B 48%
C 54%
diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

1,4-Divinylbenzene
105-06-6

1,4-Divinylbenzene

di-tert-butyl nitroxide
2406-25-9, 44871-19-4

di-tert-butyl nitroxide

2-(isopropyloxycarbonyloxy)-1-(di-t-butylnitroxy)-1-(4'-vinylphenyl)ethane

2-(isopropyloxycarbonyloxy)-1-(di-t-butylnitroxy)-1-(4'-vinylphenyl)ethane

Conditions
ConditionsYield
at 0 - 55℃; for 5h;53.2%
diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

benzylidene-(2-methylsulfanyl-phenyl)-amine
19860-20-9

benzylidene-(2-methylsulfanyl-phenyl)-amine

A

2-Phenylbenzothiazole
883-93-2

2-Phenylbenzothiazole

B

benzaldehyde
100-52-7

benzaldehyde

C

(2-aminophenyl)thiomethyl isopropyl carbonate
142505-43-9

(2-aminophenyl)thiomethyl isopropyl carbonate

Conditions
ConditionsYield
In benzene at 60℃; for 5h;A 17%
B 35%
C 53%
diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

N-(3-nitrophenylmethylene)-2-methylthiobenzenamine
142505-40-6

N-(3-nitrophenylmethylene)-2-methylthiobenzenamine

A

2-(3-nitrophenyl)benzothiazole
22868-33-3

2-(3-nitrophenyl)benzothiazole

B

3-nitro-benzaldehyde
99-61-6

3-nitro-benzaldehyde

C

(2-aminophenyl)thiomethyl isopropyl carbonate
142505-43-9

(2-aminophenyl)thiomethyl isopropyl carbonate

D

<(2-(3-nitrophenyl)methylenamino)phenyl>thiomethyl isopropyl carbonate
142505-44-0

<(2-(3-nitrophenyl)methylenamino)phenyl>thiomethyl isopropyl carbonate

Conditions
ConditionsYield
With 2,6-di-tert-butylphenol In benzene at 60℃; for 5h;A 3%
B 13%
C 10%
D 50%
diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

[4-(benzylideneamino)phenyl]methanol
783-08-4

[4-(benzylideneamino)phenyl]methanol

A

methyl 6-methoxy-2-phenylquinoline-4-carboxylate
128220-34-8

methyl 6-methoxy-2-phenylquinoline-4-carboxylate

B

carbamic acid, (4-methoxyphenyl)-, 1-methylethyl ester
85221-16-5

carbamic acid, (4-methoxyphenyl)-, 1-methylethyl ester

Conditions
ConditionsYield
With acrylic acid methyl ester In benzene at 60℃; for 4h;A 49%
B 14%
diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

N-(4-methoxyphenylmethylene)-2-methylthiobenzenamine
142505-39-3

N-(4-methoxyphenylmethylene)-2-methylthiobenzenamine

A

2-(4-methoxy-phenyl)-benzothiazole
6265-92-5

2-(4-methoxy-phenyl)-benzothiazole

B

4-methoxy-benzaldehyde
123-11-5

4-methoxy-benzaldehyde

C

(2-aminophenyl)thiomethyl isopropyl carbonate
142505-43-9

(2-aminophenyl)thiomethyl isopropyl carbonate

Conditions
ConditionsYield
In benzene at 60℃; for 5h;A 28%
B 48%
C 39%
diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

N-(phenylmethylene)-5-amino-2-methoxypyridine
123534-01-0

N-(phenylmethylene)-5-amino-2-methoxypyridine

diethylazodicarboxylate
1972-28-7

diethylazodicarboxylate

A

diethyl hydrazodicarboxylate
4114-28-7

diethyl hydrazodicarboxylate

B

(6-Methoxy-pyridin-3-yl)-carbamic acid isopropyl ester

(6-Methoxy-pyridin-3-yl)-carbamic acid isopropyl ester

C

7-Methoxy-3-phenyl-pyrido[3,2-e][1,2,4]triazine-1,2-dicarboxylic acid diethyl ester

7-Methoxy-3-phenyl-pyrido[3,2-e][1,2,4]triazine-1,2-dicarboxylic acid diethyl ester

Conditions
ConditionsYield
In benzene at 60℃;A n/a
B n/a
C 47%
diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

N-(2-thienylmethylene)-2-methylthiobenzenamine
142505-41-7

N-(2-thienylmethylene)-2-methylthiobenzenamine

A

thiophene-2-carbaldehyde
98-03-3

thiophene-2-carbaldehyde

B

2-thiophen-2-yl-benzothiazole
34243-38-4

2-thiophen-2-yl-benzothiazole

C

(2-aminophenyl)thiomethyl isopropyl carbonate
142505-43-9

(2-aminophenyl)thiomethyl isopropyl carbonate

Conditions
ConditionsYield
In benzene at 60℃; for 5h;A 40%
B 13%
C 45%
diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

1,4-Divinylbenzene
105-06-6

1,4-Divinylbenzene

2-(isopropyloxycarbonyloxy)-1-(4'-hydroxy-2',2',6',6'-tetramethyl-1'-piperidinyloxy)-1-(4'-vinylphenyl)ethane
262616-12-6

2-(isopropyloxycarbonyloxy)-1-(4'-hydroxy-2',2',6',6'-tetramethyl-1'-piperidinyloxy)-1-(4'-vinylphenyl)ethane

Conditions
ConditionsYield
at 0 - 55℃; for 5h;41%
diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

[4-(benzylideneamino)phenyl]methanol
783-08-4

[4-(benzylideneamino)phenyl]methanol

A

carbamic acid, (4-methoxyphenyl)-, 1-methylethyl ester
85221-16-5

carbamic acid, (4-methoxyphenyl)-, 1-methylethyl ester

B

Benzoyl-(4-methoxy-phenyl)-carbamic acid isopropyl ester

Benzoyl-(4-methoxy-phenyl)-carbamic acid isopropyl ester

C

6-Methoxy-2,3,4-triphenyl-quinoline

6-Methoxy-2,3,4-triphenyl-quinoline

Conditions
ConditionsYield
With (E)-1,2-diphenyl-ethene In benzene at 60℃; for 4h;A 15%
B 40%
C 20%
diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

N-(3-nitrophenylmethylene)-2-methylthiobenzenamine
142505-40-6

N-(3-nitrophenylmethylene)-2-methylthiobenzenamine

A

2-(3-nitrophenyl)benzothiazole
22868-33-3

2-(3-nitrophenyl)benzothiazole

B

3-nitro-benzaldehyde
99-61-6

3-nitro-benzaldehyde

C

(2-aminophenyl)thiomethyl isopropyl carbonate
142505-43-9

(2-aminophenyl)thiomethyl isopropyl carbonate

Conditions
ConditionsYield
In benzene at 60℃; for 5h;A 38%
B 40%
C 35%
diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

A

carbamic acid, phenyl-, 1-methylethyl ester
122-42-9

carbamic acid, phenyl-, 1-methylethyl ester

B

2-phenyl-quinoline-3,4-dicarbonitrile
57464-22-9

2-phenyl-quinoline-3,4-dicarbonitrile

Conditions
ConditionsYield
With 1,2-Dicyanoethylene In benzene at 60℃; for 4h;A 20%
B 38%
diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

N-(3-phenyl-2-propenylidene)-2-methylthiobenzenamine
142505-42-8

N-(3-phenyl-2-propenylidene)-2-methylthiobenzenamine

A

2-styrylbenzothiazole
1483-30-3, 59066-61-4, 104505-71-7

2-styrylbenzothiazole

B

(2-aminophenyl)thiomethyl isopropyl carbonate
142505-43-9

(2-aminophenyl)thiomethyl isopropyl carbonate

C

3-phenyl-propenal
104-55-2

3-phenyl-propenal

Conditions
ConditionsYield
In benzene at 60℃; for 5h;A 24%
B 30%
C 36%
diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

4-{[1-(4-Methoxy-phenyl)-meth-(E)-ylidene]-amino}-benzoic acid ethyl ester

4-{[1-(4-Methoxy-phenyl)-meth-(E)-ylidene]-amino}-benzoic acid ethyl ester

diethylazodicarboxylate
1972-28-7

diethylazodicarboxylate

A

diethyl hydrazodicarboxylate
4114-28-7

diethyl hydrazodicarboxylate

B

4-Isopropoxycarbonylamino-benzoic acid ethyl ester

4-Isopropoxycarbonylamino-benzoic acid ethyl ester

C

3-(4-Methoxy-phenyl)-benzo[1,2,4]triazine-1,2,7-tricarboxylic acid triethyl ester

3-(4-Methoxy-phenyl)-benzo[1,2,4]triazine-1,2,7-tricarboxylic acid triethyl ester

Conditions
ConditionsYield
In benzene at 60℃;A n/a
B n/a
C 36%
diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

9-methylene-fluorene
4425-82-5

9-methylene-fluorene

polymer, Mn 1070 by SEC with oligostyrene as standard, Mn 1560 by SEC with oligo(dibenzofulvene) as standard; monomer(s): dibenzofulvene; 2,9-dimethyl-3,5,6,8-tetraoxadeca-4,7-dione

polymer, Mn 1070 by SEC with oligostyrene as standard, Mn 1560 by SEC with oligo(dibenzofulvene) as standard; monomer(s): dibenzofulvene; 2,9-dimethyl-3,5,6,8-tetraoxadeca-4,7-dione

Conditions
ConditionsYield
In toluene at 40℃; for 24h;33%
diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

N-(4-chlorophenylmethylene)-N'-methyl-N'-phenylbenzen-1,2-diamine

N-(4-chlorophenylmethylene)-N'-methyl-N'-phenylbenzen-1,2-diamine

A

1-phenyl-2-(4-chlorophenyl)-1H-benzo[d]imidazole
2622-73-3

1-phenyl-2-(4-chlorophenyl)-1H-benzo[d]imidazole

B

3-(4-chlorophenyl)-1-phenyl-1H-quinoxalin-2-one

3-(4-chlorophenyl)-1-phenyl-1H-quinoxalin-2-one

C

3-phenylbenzimidazolin-2-one-1-carboxylic acid 2-propyl ester

3-phenylbenzimidazolin-2-one-1-carboxylic acid 2-propyl ester

Conditions
ConditionsYield
In benzene at 60℃; for 18h;A 16%
B 28%
C 11%
diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

N-(4-chlorobenzylidene)aniline
780-21-2

N-(4-chlorobenzylidene)aniline

A

Isopropyl N-4-chlorophenylcarbamate
2239-92-1

Isopropyl N-4-chlorophenylcarbamate

B

methyl 6-chloro-2-phenylquinoline-4-carboxylate

methyl 6-chloro-2-phenylquinoline-4-carboxylate

Conditions
ConditionsYield
With acrylic acid methyl ester In benzene at 60℃; for 4h;A 27%
B 16%
diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

N-benzylidene-4-acetylaniline
138469-40-6

N-benzylidene-4-acetylaniline

A

isopropyl (4-acetylphenyl)carbamate
67648-20-8

isopropyl (4-acetylphenyl)carbamate

B

6-Acetyl-2-phenyl-quinoline-4-carbonitrile

6-Acetyl-2-phenyl-quinoline-4-carbonitrile

Conditions
ConditionsYield
With acrylonitrile In benzene at 60℃; for 4h;A 23%
B 27%
diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

N-(4-chlorophenylmethylene)-2-<4-(triphenylmethoxy)phenoxy>benzeneamine

N-(4-chlorophenylmethylene)-2-<4-(triphenylmethoxy)phenoxy>benzeneamine

A

triphenylmethyl alcohol
76-84-6

triphenylmethyl alcohol

B

2-(4-chlorophenyl)benzoxazole
1141-35-1

2-(4-chlorophenyl)benzoxazole

C

triphenylmethyl iso-propyl ether
13594-78-0

triphenylmethyl iso-propyl ether

D

2-propyl 4-(triphenylmethoxy)phenyl carbonate

2-propyl 4-(triphenylmethoxy)phenyl carbonate

Conditions
ConditionsYield
In benzene at 60℃; for 24h; Further byproducts given;A 23%
B 23%
C 6%
D 6%
diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

N-(4-chlorophenylmethylene)-2-<4-(triphenylmethoxy)phenoxy>benzeneamine

N-(4-chlorophenylmethylene)-2-<4-(triphenylmethoxy)phenoxy>benzeneamine

A

triphenylmethyl alcohol
76-84-6

triphenylmethyl alcohol

B

2-(4-chlorophenyl)benzoxazole
1141-35-1

2-(4-chlorophenyl)benzoxazole

C

triphenylmethyl iso-propyl ether
13594-78-0

triphenylmethyl iso-propyl ether

D

2-propyl 4-(triphenylmethoxy)phenyl carbonate

2-propyl 4-(triphenylmethoxy)phenyl carbonate

E

11-(4-chlorophenyl)-2-(triphenylmethoxy)dibenz<1,4>oxazepine

11-(4-chlorophenyl)-2-(triphenylmethoxy)dibenz<1,4>oxazepine

Conditions
ConditionsYield
In benzene at 60℃; for 24h; Product distribution; Mechanism;A 23%
B 23%
C 6%
D 6%
E 3%
diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

N-(4-methoxyphenylmethylene)-N'-methyl-N'-phenylbenzen-1,2-diamine

N-(4-methoxyphenylmethylene)-N'-methyl-N'-phenylbenzen-1,2-diamine

A

3-phenylbenzimidazolin-2-one-1-carboxylic acid 2-propyl ester

3-phenylbenzimidazolin-2-one-1-carboxylic acid 2-propyl ester

B

3-(4-methoxyphenyl)-1-phenyl-1H-quinoxalin-2-one

3-(4-methoxyphenyl)-1-phenyl-1H-quinoxalin-2-one

C

2-(4-methoxyphenyl)-1-phenyl-1H-benzo[d]imidazole
2620-84-0

2-(4-methoxyphenyl)-1-phenyl-1H-benzo[d]imidazole

Conditions
ConditionsYield
In benzene at 60℃; for 18h;A 18%
B 21%
C 13%
diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

phenylacetylene
536-74-3

phenylacetylene

(4-Methoxy-phenyl)-[2-methyl-2-phenyl-prop-(E)-ylidene]-amine

(4-Methoxy-phenyl)-[2-methyl-2-phenyl-prop-(E)-ylidene]-amine

A

(1-isopropoxyethyl)benzene
65757-61-1

(1-isopropoxyethyl)benzene

B

1-Phenylethanol
98-85-1, 13323-81-4

1-Phenylethanol

C

(Z)-3-(4-methoxyphenyl)-3-phenyl-2-propenenitrile

(Z)-3-(4-methoxyphenyl)-3-phenyl-2-propenenitrile

D

1,1-Dimethyl-4-phenyl-1H-naphthalen-2-one

1,1-Dimethyl-4-phenyl-1H-naphthalen-2-one

E

7-Methoxy-2-(1-methyl-1-phenyl-ethyl)-4-phenyl-quinoline

7-Methoxy-2-(1-methyl-1-phenyl-ethyl)-4-phenyl-quinoline

F

6-Methoxy-2-(1-methyl-1-phenyl-ethyl)-4-phenyl-quinoline

6-Methoxy-2-(1-methyl-1-phenyl-ethyl)-4-phenyl-quinoline

Conditions
ConditionsYield
In benzene at 60℃; Product distribution; Mechanism; same produts were determined by GC;A n/a
B n/a
C 21%
D n/a
E n/a
F n/a
diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

A

Benzoyl-phenyl-carbamic acid isopropyl ester
5892-72-8

Benzoyl-phenyl-carbamic acid isopropyl ester

B

2-phenyl-4-(trimethylsilyl)quinoline
128220-30-4

2-phenyl-4-(trimethylsilyl)quinoline

Conditions
ConditionsYield
With ethenyltrimethylsilane In benzene at 60℃; for 4h;A 20%
B 7%
diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

N-(phenylmethylene)-N'-methyl-N'-phenylbenzen-1,2-diamine

N-(phenylmethylene)-N'-methyl-N'-phenylbenzen-1,2-diamine

A

1,2-diphenyl-1H-benzoimidazole
2622-67-5

1,2-diphenyl-1H-benzoimidazole

B

3-phenylbenzimidazolin-2-one-1-carboxylic acid 2-propyl ester

3-phenylbenzimidazolin-2-one-1-carboxylic acid 2-propyl ester

C

1,3-diphenyl-1H-quinoxalin-2-one
16194-28-8

1,3-diphenyl-1H-quinoxalin-2-one

Conditions
ConditionsYield
In benzene at 60℃; for 30h;A 20%
B 14%
C 14%
diisopropyl peroxydicarbonate
105-64-6

diisopropyl peroxydicarbonate

N-(4-methoxyphenylmethylene)-2-phenoxybenzeneamine

N-(4-methoxyphenylmethylene)-2-phenoxybenzeneamine

A

4-Methoxybenzophenone
611-94-9

4-Methoxybenzophenone

B

4-methoxy-benzaldehyde
123-11-5

4-methoxy-benzaldehyde

C

11-(4-methoxyphenyl)dibenz<1,4>oxazepine
124293-56-7

11-(4-methoxyphenyl)dibenz<1,4>oxazepine

D

2-propyl N-(2-phenoxyphenyl)carbamate

2-propyl N-(2-phenoxyphenyl)carbamate

Conditions
ConditionsYield
In benzene at 60℃; for 6h; imine:reagent=1:4; Yield given. Further byproducts given;A 18%
B n/a
C 17%
D n/a

105-64-6Upstream product

105-64-6Relevant articles and documents

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Adam,W.,Rios,A.

, p. 407 - 411 (1971)

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METHOD FOR THE PRODUCTION OF ORGANIC PEROXIDES BY MEANS OF A MICROREACTION TECHNIQUE

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Page/Page column 7, (2009/03/07)

The invention provides a process for efficient and reliable preparation of organic peroxides, preferably dialkyl peroxides, peroxycarboxylic acids, peroxycarboxylic esters, diacyl peroxides, peroxycarbonate esters, peroxydicarbonates, ketone peroxides and perketals with the aid of at least one static micromixer and an apparatus for performing the process.

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