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Hunan Russell Chemicals Technology Co.,Ltd

high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:any port in China

1-Propene, 3-chloro- 107-05-1

Cas:107-05-1

Min.Order:0

Negotiable

Type:Trading Company

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Amadis Chemical Co., Ltd.

1.Professional synthesis laboratory and production base. 2.Strong synthesis team and service team. 3.Professional data management system. 4.We provide the professional test date and product information ,ex. HNMR ,CNMR,FNMR, HPLC/G

Amadis Chemical offer CAS#107-05-1;CAT#A801564

Cas:107-05-1

Min.Order:10 Milligram

Negotiable

Type:Lab/Research institutions

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QINGDAO ON-BILLION INDUSTRAIL CO.,LTD

Stability Stable, but reacts vigorously or violently with a wide variety of materials. Highly flammable. Incompatible with strong oxidizing agents, acids, amines, peroxides, chlorides of iron and aluminium, BF3, aromatic hydrocarbons, Lewis aci

Allyl chloride

Cas:107-05-1

Min.Order:25 Kilogram

Negotiable

Type:Trading Company

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Shandong Jiading Chemical Co.,ltd

Our advantage: 1. Higest quality and good package 2.Fast delivery 3.Better payment term 4.Fast response to customer within 6 hours 5.Good business credit in Europe ,US ,Japan ,Korea Anyway ,if you need any chemicals from China ,Shandong

High quality Allyl chloride supplier in China CAS NO.107-05-1

Cas:107-05-1

Min.Order:1 Kilogram

FOB Price: $1750.0 / 1900.0

Type:Trading Company

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Zouping Sanhao Chemical Co., Ltd .

allyl chloride CAS#:107-05-1 tructural formula:C3H5Cl Physical property: nature colorless flammable liquids, corrosive and irritant scent. The relative density of 0.9382 (20 / 4 ° C). Solidification point -134.5 ° C The boiling point o

allyl chloride (CAS No.: 107-05-1)

Cas:107-05-1

Min.Order:100 Kilogram

Negotiable

Type:Trading Company

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Pure Chemistry Scientific Inc.

1-Propene, 3-chloro- Application:80063044

1-Propene, 3-chloro-

Cas:107-05-1

Min.Order:1 Gram

FOB Price: $500.0

Type:Trading Company

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Synthetic route

2-propynyl chloride
624-65-7

2-propynyl chloride

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

3-chloroprop-1-ene

Conditions
ConditionsYield
With piperazine; hydrogen In ethanol at 80℃; under 4500.45 Torr; for 24h;99%
With piperazine; hydrogen In ethanol at 100℃; under 4500.45 Torr; for 15h; Green chemistry;
With hydrogen In ethanol at 100℃; under 4500.45 Torr; for 24h; chemoselective reaction;87 %Chromat.
π-allyl(dichloro)(pentamethylcyclopentadienyl)ruthenium (IV)

π-allyl(dichloro)(pentamethylcyclopentadienyl)ruthenium (IV)

A

(η(5)-C5Me5)Ru(CO)2Cl

(η(5)-C5Me5)Ru(CO)2Cl

B

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

3-chloroprop-1-ene

Conditions
ConditionsYield
With CO In decane (CO); heating (2 h, 140°C), cooling; chromy. (silica gel, ether);A 96%
B n/a
With CO In decane (CO); heating (2 h, 120°C), cooling; chromy. (silica gel, ether);A 16%
B n/a
N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

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

3-chloroprop-1-ene

Conditions
ConditionsYield
With 2-chloro-4,6-dimethoxy-1 ,3,5-triazine In toluene Reflux;96%
Ru(η5-C5H5)(η3-C3H5)Cl2

Ru(η5-C5H5)(η3-C3H5)Cl2

A

(η(5)-cyclopentadienyl)dicarbonylchlororuthenium(II)

(η(5)-cyclopentadienyl)dicarbonylchlororuthenium(II)

B

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

3-chloroprop-1-ene

Conditions
ConditionsYield
With CO In decane (CO); heating (2 h, 140°C), cooling; chromy. (silica gel, ether);A 93%
B n/a
propene
187737-37-7

propene

A

2-chloropropene
557-98-2

2-chloropropene

B

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

1,2-Dichloropropane

C

E/Z-1,3-Dichloropropene
542-75-6

E/Z-1,3-Dichloropropene

D

isopropyl chloride
75-29-6

isopropyl chloride

E

propenyl chloride
590-21-6

propenyl chloride

F

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

3-chloroprop-1-ene

Conditions
ConditionsYield
With aluminum oxide; copper dichloride; dibenzoyl peroxide at 489.9℃; for 0.000555556h; Product distribution; Mechanism; also other temperatures (503 K - 753 K) and initiators (chloral dioxyperoxide);A 0.7%
B 3.3%
C 0.8%
D 1.8%
E 0.9%
F 91.4%
cis,trans-[Ir(Cl3)(-CH=CHPPh3)2(CO)(PPh3)2](ClO4)2

cis,trans-[Ir(Cl3)(-CH=CHPPh3)2(CO)(PPh3)2](ClO4)2

allyl bromide
106-95-6

allyl bromide

cis,cis-[IrBr2(CH3)(-CH=CHPPh3)2(CO)(PPh3)](ClO4)

cis,cis-[IrBr2(CH3)(-CH=CHPPh3)2(CO)(PPh3)](ClO4)

B

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

3-chloroprop-1-ene

Conditions
ConditionsYield
In chloroform A mixt. of reagents in CHCl3 was stirred at 50°C for 2 days, cooled to room temp.;; elem. anal.;;A 91%
B n/a
Ru(η5-C5H5)(η3-C3H5)Cl2

Ru(η5-C5H5)(η3-C3H5)Cl2

para-xylene
106-42-3

para-xylene

A

(η5-C5H5)Ru(p-xylene)Cl

(η5-C5H5)Ru(p-xylene)Cl

B

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

3-chloroprop-1-ene

Conditions
ConditionsYield
(N2); heating (17 h, 140°C), cooling; concn., chromy. (silica gel, MeOH);A 88%
B n/a
epichlorohydrin
106-89-8

epichlorohydrin

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

3-chloroprop-1-ene

Conditions
ConditionsYield
With zirconium(IV) chloride; sodium iodide In acetonitrile for 0.0166667h; Heating;87%
With Silphos; iodine In N,N-dimethyl-formamide at 20℃; for 0.416667h;74%
With iodine; triphenylphosphine In N,N-dimethyl-formamide at 20℃;
With hydrogen; triethyl phosphite In isopropyl alcohol at 100℃; under 4500.45 Torr; for 12h; Glovebox; chemoselective reaction;85 %Chromat.
allyl phenyl ether
1746-13-0

allyl phenyl ether

A

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

3-chloroprop-1-ene

B

phenol
108-95-2

phenol

Conditions
ConditionsYield
With bis(benzonitrile)palladium(II) dichloride In benzene for 20h; Product distribution; Heating; further subst.; use of deallylation as deprotection of phenolic hydroxyl groups;A n/a
B 86%
N-allyl-N-cyclohexylmethylamine
22416-98-4

N-allyl-N-cyclohexylmethylamine

2,2,2-Trichloroethyl chloroformate
17341-93-4

2,2,2-Trichloroethyl chloroformate

A

Cyclohexyl-methyl-carbamic acid 2,2,2-trichloro-ethyl ester
87876-79-7

Cyclohexyl-methyl-carbamic acid 2,2,2-trichloro-ethyl ester

B

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

3-chloroprop-1-ene

Conditions
ConditionsYield
In benzene Heating;A 85%
B n/a
hexyl 2-propenyl ether
3295-94-1

hexyl 2-propenyl ether

phenylacetyl chloride
103-80-0

phenylacetyl chloride

A

Phenylessigsaeurehexylester
5421-17-0

Phenylessigsaeurehexylester

B

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

3-chloroprop-1-ene

Conditions
ConditionsYield
With zinc In Petroleum ether at 28℃; for 2h;A 85%
B n/a
cyclopropane
75-19-4

cyclopropane

A

cyclopropyl chloride
7393-45-5

cyclopropyl chloride

B

1,1-dichlorocyclopropane
2088-35-9

1,1-dichlorocyclopropane

C

1,3-Dichloropropane
142-28-9

1,3-Dichloropropane

D

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

3-chloroprop-1-ene

Conditions
ConditionsYield
With chlorine; silicon tetrafluoride at 600℃; Product distribution; Irradiation;A 83.5%
B 4%
C n/a
D 2.6%
allyl alcohol
107-18-6

allyl alcohol

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

3-chloroprop-1-ene

Conditions
ConditionsYield
With benzoyl chloride; N,N-dimethyl-formamide at 0 - 20℃; for 5.5h;82%
With hydrogenchloride; sulfuric acid; copper(l) chloride75.4%
With priphenylchlorophosphonium phosphorodichloridate at 20℃; Arbuzov reaction;75%
allyl diphenyl phosphate
19206-69-0

allyl diphenyl phosphate

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

3-chloroprop-1-ene

Conditions
ConditionsYield
With lithium chloride In N,N-dimethyl-formamide for 0.166667h; Ambient temperature;75%
N,N-dimethyl-formamide
68-12-2, 33513-42-7

N,N-dimethyl-formamide

epichlorohydrin
106-89-8

epichlorohydrin

A

formic acid 1-bromomethyl-2-chloroethyl ester
101257-40-3

formic acid 1-bromomethyl-2-chloroethyl ester

B

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

3-chloroprop-1-ene

Conditions
ConditionsYield
With bromine; triphenylphosphine at 0℃; for 1h;A 75%
B n/a
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