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Cas:927-83-3
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inquiryAppearance:- Storage:R.T Package:1kg/bottle Application:Organic reagents Transportation:Express/Sea/Air Port:Any port in China
Cas:927-83-3
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
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Cas:927-83-3
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
inquirysuperior quality moderate price & quick delivery Appearance:powder Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bag, 1kg/drum or 25kg/drum or as per your request. Application:Used to make other chemica
Cas:927-83-3
Min.Order:1 Kilogram
Negotiable
Type:Trading Company
inquiry1. Product advantages ♦ High purity, all above 98.5%, no impurities after dissolution ♦ We will test each batch to ensure quality ♦ OEM and private brand services designed for free ♦ Various cap colors available ♦ W
Cas:927-83-3
Min.Order:1 Kilogram
FOB Price: $7.0 / 9.0
Type:Trading Company
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Cas:927-83-3
Min.Order:1 Kilogram
FOB Price: $2.0
Type:Lab/Research institutions
inquiryHunan chemfish Pharmaceutical co.,Ltd.located in Lugu High-tech industral park ,Hunan province . with its own R&D center and more than 10000㎡manufacture plant . Chemfish owns 40 reactors from 1000L to 8000L. With complete auxiliary equipment as
We are committed to providing our customers with the best products and services at the most competitive prices.Appearance:beige crystalline powder Storage:Room temperature with sealed well Package:according to the clients requirement Application:Use
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
FINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the AZO-TERT-BUTANE, CAS:927-83-3 with the most competitive price and the best quality. W
1,2-di-tert-butylhydrazine
di-t-butyldiazene
Conditions | Yield |
---|---|
at 20℃; for 72h; Air; Darkness; | 66% |
iron pentacarbonyl
t-butylnitrite
A
di-t-butyldiazene
B
1,3-di-tert-butylcarbodiimide
C
1,3-di-tert-butylurea
D
di-t-butyldiazene N-oxide
Conditions | Yield |
---|---|
In tetrahydrofuran Irradiation (UV/VIS); Stirring of nitroso compound in THF under N2, metal carbonyl in THF is added, the soln. is irradiated for 1 h (sunlamp photolysis) at 30°C.; addn. of naphthalene as internal standard, Gc-anal.; | A 1% B 1% C 13% D 4% |
N-bromo-2-methylpropan-2-amine
di-t-butyldiazene
Conditions | Yield |
---|---|
With silver(l) oxide |
Conditions | Yield |
---|---|
With diethyl ether; dinitrogen monoxide |
nitrobenzene
tert-butylamine
A
di-t-butyldiazene
B
N-Phenylhydroxylamine
C
azoxybenzene
Conditions | Yield |
---|---|
Mechanism; Rate constant; Irradiation; reaction also in presence of biacetyl and benzophenone or O2; |
tert-butylamine
A
di-t-butyldiazene
B
N-Phenylhydroxylamine
C
azoxybenzene
Conditions | Yield |
---|---|
With nitrobenzene Irradiation; also in presence of biacetyl and benzophenone; |
N-tert-butyl-α-phenylnitrone
1,3,5-trimethyl hexachloro cyclotrigermazane
A
(Cl2GeO)3
B
di-t-butyldiazene
C
N-Benzylidenemethylamine
Conditions | Yield |
---|---|
Kinetics; react. of germazane with nitron with and without catalysis; |
N-tert-butyl-α-phenylnitrone
nonamethyl cyclotrigermazane
A
di-t-butyldiazene
B
2,2,4,4,6,6-hexamethyl-1,3,5-trioxa-2,4,6-trigermacyclohexane
C
N-Benzylidenemethylamine
Conditions | Yield |
---|---|
Kinetics; react. of germazane with nitron, depending on catalysator; |
A
tert-butyl isocyanide
B
di-t-butyldiazene
C
tert-butylisonitrile
Conditions | Yield |
---|---|
In Cyclohexane-d12 at 180℃; for 0.133333h; |
A
di-t-butyldiazene
B
Mn4IV(μ3-NtBu)4(NtBu)4
Conditions | Yield |
---|---|
With tetraethylammonium chloride Inert atmosphere; |
A
di-t-butyldiazene
B
Mn4IV(μ3-NtBu)4(NtBu)4
Conditions | Yield |
---|---|
With tetraethylammonium chloride In tetrahydrofuran; acetonitrile at 120℃; for 24h; Solvent; Inert atmosphere; | A n/a B 81 %Spectr. |
A
4-amino-N-methylphthalimide
B
4-(methylamino)butyric acid
C
di-t-butyldiazene
D
N-nitroso-1-phenylmethanamine
E
phthiocol
F
Phthalic acid dibutyl ester
G
N,N'-bis(allyl)-1,4-benzene dicarboxamide
I
1,2,4,5-tetrazine-3-amine
J
3-Hydroxybutyric acid
Conditions | Yield |
---|---|
Stage #1: 6-(acetylamino)-4-hydroxy-3-[[4-[[2-(sulfooxy)ethyl]sulfonyl]phenyl]azo]-2-naphthalenesulfonic acid disodium salt With sodium sulfate In water for 4h; Inert atmosphere; Electrochemical reaction; Stage #2: In methanol for 16h; |
Conditions | Yield |
---|---|
In tetrahydrofuran at -80 - 20℃; for 2.25h; Inert atmosphere; Schlenk technique; Glovebox; |
di-t-butyldiazene
N,N'-di-tert-butylhydrazine hydrochloride
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In acetic acid under 45003.6 Torr; for 15h; | 88% |
di-t-butyldiazene
1,2-di-tert-butylhydrazinium perchlorate
Conditions | Yield |
---|---|
With sodium perchlorate; hydrogen; palladium on activated charcoal In acetic acid under 45003.6 Torr; for 15h; | 88% |
Conditions | Yield |
---|---|
In benzene at 90℃; for 24h; Inert atmosphere; Glovebox; | 71% |
di-t-butyldiazene
A
(3,3-dimethylbutyl)benzene
B
tert-butyl 2-phenylethyl ether
Conditions | Yield |
---|---|
In tetrahydrofuran at 180℃; for 18h; Sealed tube; | A 50% B 30% |
Conditions | Yield |
---|---|
In benzene for 24h; Ambient temperature; Irradiation; | A 39% B 40% |
Conditions | Yield |
---|---|
With thianthrene cation radical perchlorate Ambient temperature; | 25.6% |
di-t-butyldiazene
2,4-di-t-butyl-6-methylnitrosobenzene
Conditions | Yield |
---|---|
In benzene at 0 - 5℃; for 1h; Mechanism; Irradiation; | A 8% B 6% C 23% |
In benzene at 0 - 5℃; for 1h; Irradiation; | A 8% B 6% C 23% |
Conditions | Yield |
---|---|
With Di-n-octyl phthalate at 200℃; |
di-t-butyldiazene
2-isopropyl-3,3-dimethyl-1-nitro-but-1-ene
C13H26NO
Conditions | Yield |
---|---|
Irradiation; |
Conditions | Yield |
---|---|
Irradiation; |
di-t-butyldiazene
1,2-di-tert-butylhydrazine
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In acetic acid |
2,2,6,6-Tetramethyl-1-piperidinyloxy free radical
di-t-butyldiazene
1‐(tert‐butoxy)‐2,2,6,6‐tetramethylpiperidine
Conditions | Yield |
---|---|
In pentane for 2h; Ambient temperature; Irradiation; | |
In benzene-d6 Irradiation; |
di-t-butyldiazene
N,N’-(ethane-1,2-diylidene)bis(2-methylpropan-2-amine N-oxide)
C14H29N2O2
Conditions | Yield |
---|---|
In dichloromethane Irradiation; |
di-t-butyldiazene
1,3,5-tribromo-2-nitroso-benzene
2,4,6-Tribromophenyl-t-butyl-nitroxid-Radikal
Conditions | Yield |
---|---|
In benzene 1.) 60 deg C, 3 min, 2.) to 25 deg C, 2 min; |
Conditions | Yield |
---|---|
In chlorobenzene at 23℃; Irradiation; |
Conditions | Yield |
---|---|
In benzene Ambient temperature; Irradiation; |
di-t-butyldiazene
A
methanol
B
tert.-butylhydroperoxide
C
di-tert-butyl peroxide
D
acetone
E
tert-butyl alcohol
Conditions | Yield |
---|---|
With oxygen at 59.9℃; Quantum yield; Mechanism; Irradiation; Other temperatures (298, 373 K), the effect of added t-butyl hydroperoxide.; |
di-t-butyldiazene
Conditions | Yield |
---|---|
With crotyl-K In tetrahydrofuran Irradiation; |
di-t-butyldiazene
para-methylbenzonitrile
toluene
A
1,2-bis-(4-cyanophenyl)ethane
B
(2,2-dimethyl-1-propyl)benzene
C
1-(4-cyanophenyl)-2-phenylethane
D
1,1'-(1,2-ethanediyl)bisbenzene
Conditions | Yield |
---|---|
at 80℃; for 20h; Product distribution; Irradiation; |
di-t-butyldiazene
m-xylene
toluene
A
1-(2,2-dimethylpropyl)-2-methylbenzene
B
(2,2-dimethyl-1-propyl)benzene
C
1,2-di-m-tolylethane
D
1-(3-methylphenyl)-2-phenylethane
E
1,1'-(1,2-ethanediyl)bisbenzene
Conditions | Yield |
---|---|
at 80℃; for 20h; Product distribution; Irradiation; |
di-t-butyldiazene
para-xylene
toluene
A
1,2-di-p-tolylethane
B
4-methyl-1-(2,2-dimethylpropyl)benzene
C
(2,2-dimethyl-1-propyl)benzene
D
4-methylbibenzyl
E
1,1'-(1,2-ethanediyl)bisbenzene
Conditions | Yield |
---|---|
at 80℃; for 20h; Product distribution; Irradiation; |
di-t-butyldiazene
1-chloro-3-methylbenzene
toluene
A
1-Chlor-3-neopentyl-benzol
B
(2,2-dimethyl-1-propyl)benzene
C
1,2-bis(3-chlorophenyl)ethane
D
3-chloro-bibenzyl
E
1,1'-(1,2-ethanediyl)bisbenzene
Conditions | Yield |
---|---|
at 80℃; for 20h; Product distribution; Irradiation; |
di-t-butyldiazene
para-chlorotoluene
toluene
A
1-Chlor-4-(2,2-dimethylpropyl)benzol
B
(2,2-dimethyl-1-propyl)benzene
C
1,2-bis(4-chlorophenyl)ethane
D
4-chlorobibenzyl
E
1,1'-(1,2-ethanediyl)bisbenzene
Conditions | Yield |
---|---|
at 80℃; for 20h; Product distribution; Irradiation; |
di-t-butyldiazene
3,4-Dichlorotoluene
toluene
A
3,4,3',4'-tetrachloro-bibenzyl
B
(2,2-dimethyl-1-propyl)benzene
D
1,1'-(1,2-ethanediyl)bisbenzene
Conditions | Yield |
---|---|
at 80℃; for 20h; Product distribution; Irradiation; |
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