Our Advantage Rich Experience Our products are sold all over Europe,North&South America, Sino-East, Asia and pacific area as well as Africa,we establish long term. Quality service Company cooperates with research institutes. We strictly con
Cas:27208-37-3
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FOB Price: $1.0 / 10.0
Type:Trading Company
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Min.Order:1 Gram
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Type:Lab/Research institutions
inquiryCYCLOPENTA(C,D)PYRENE CAS:27208-37-3 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic int
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Min.Order:1 Gram
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Type:Lab/Research institutions
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Min.Order:1 Kilogram
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Type:Lab/Research institutions
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Cas:27208-37-3
Min.Order:10 Gram
FOB Price: $100.0
Type:Lab/Research institutions
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Min.Order:1 Metric Ton
FOB Price: $7.0 / 8.0
Type:Trading Company
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Known for its best quality and competitve price, this chemicals we offered is widely appreciated by our customers.Appearance:White powder Storage:keep sealed and keep from direct light Package:According client's requirements Application:pharmaceutica
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Min.Order:0
Negotiable
Type:Trading Company
inquiryfactory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
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Cas:27208-37-3
Min.Order:1 Gram
Negotiable
Type:Trading Company
inquiryHenan Wising Chem specialize in sourcing the chemicals in China. We are associated with many trusted manufacturers each having different area of expertise required for meeting the needs of our local as well as overseas buyers . We have access to cu
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Min.Order:500 Gram
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FINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the CYCLOPENTA(C,D)PYRENE, CAS:27208-37-3 with the most competitive price and the best qu
Cyclopenta(C,D)Pyrene manufacturerAppearance:White powder Storage:keep in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/pharma intermediate Transportation:By Sea,by Air,By courier like DHL or Fedx.
Cas:27208-37-3
Min.Order:0
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Type:Trading Company
inquiryDebyesci is here who supplied several kinds of chemical products to global pharmaceutical, drug discovery, agrochemical and biotechnology industries for four yearsOur key scientific leadership team has gained experience in top research and developmen
Cyclopenta[cd]pyreneAppearance:Off white to slight yellow solid Storage:Stored in shaded, cool and dry places Package:1L 5L 10L 25L bottle Application:pharma intermediate Transportation:Handle with cares to avoid damaging the packages. Protect them f
3,4,4a,5-tetrahydrocyclopentapyrene
cyclopenta[c,d]pyrene
Conditions | Yield |
---|---|
With 2,3-dicyano-5,6-dichloro-p-benzoquinone In toluene for 1h; Heating; | 95% |
1-(1-chlorovinyl)pyrene
cyclopenta[c,d]pyrene
Conditions | Yield |
---|---|
at 1000℃; under 0.01 Torr; | 88% |
Multi-step reaction with 2 steps 1: 600 °C / 0.01 Torr 2: 1000 °C / 0.01 Torr View Scheme |
3,9-Diethynyl-phenanthrene
A
fluoranthene
B
cyclopenta[c,d]pyrene
C
acephenanthrylene
Conditions | Yield |
---|---|
at 1000℃; under 0.01 Torr; Mechanism; var. of temp.; other polyclic aromatic hydrocarbon with ethynyl subst.; | A 2% B 1% C 4% D 8% E 85% |
Conditions | Yield |
---|---|
at 1000℃; under 0.01 Torr; Further byproducts given; | A 2% B 1% C 8% D 85% |
3-hydroxy-3,4-dihydrocyclopentapyrene
cyclopenta[c,d]pyrene
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In toluene for 1h; Heating; | 83% |
With aluminum oxide In benzene Dehydration; | 65% |
With toluene-4-sulfonic acid |
1,2,2a,3,4,6,7,8-octahydrocyclopentapyrene
cyclopenta[c,d]pyrene
Conditions | Yield |
---|---|
With 2,3-dicyano-5,6-dichloro-p-benzoquinone In toluene for 16h; Heating; | 70% |
benzo[c]phenathrene
A
phenanthrene
B
cyclopenta[c,d]pyrene
C
benzo[ghi]fluoranthene
Conditions | Yield |
---|---|
at 1150℃; under 0.5 Torr; | A 4% B 41% C 26% |
3,9-Diethynyl-phenanthrene
A
fluoranthene
B
cyclopenta[c,d]pyrene
C
acephenanthrylene
Conditions | Yield |
---|---|
at 1025℃; under 0.01 Torr; Further byproducts given; | A 7% B 8% C 16% D 12% |
3-(4H-cyclopentaphenanthrylidene)-1,5-bis(trimethylsilyl)-1,4-pentadiyne
A
pyrene
B
benzo[e]pyrene
C
4H-Cyclopenta[def]phenanthrene
D
cyclopenta[c,d]pyrene
E
benzo[ghi]fluoranthene
F
Coarannulen
Conditions | Yield |
---|---|
With hydrogen In gas at 900℃; Product distribution; electrically heated vertical laboratory tubular furnace; | A n/a B n/a C n/a D n/a E n/a F 15% |
3-(4H-cyclopentaphenanthrylidene)-1,5-bis(trimethylsilyl)-1,4-pentadiyne
A
pyrene
B
benzo[e]pyrene
C
cyclopenta[c,d]pyrene
D
Coarannulen
Conditions | Yield |
---|---|
With hydrogen In gas at 900℃; electrically heated vertical laboratory tubular furnace; Further byproducts given; | A n/a B n/a C n/a D 15% |
benzo[ghi]fluoranthene
cyclopenta[c,d]pyrene
Conditions | Yield |
---|---|
at 1175℃; | 12% |
benzo<3,4>cyclobuta<1,2-b>biphenylene
A
cyclopenta[c,d]pyrene
B
benzo[ghi]fluoranthene
C
Triangular [4]phenylene
D
cyclopenta[cd]fluoranthene
Conditions | Yield |
---|---|
Pyrolysis; Further byproducts.; | A 2% B 10% C 1% D 4% |
benzo<3,4>cyclobuta<1,2-b>biphenylene
A
cyclopenta[c,d]pyrene
B
benzo[ghi]fluoranthene
D
cyclopenta[cd]fluoranthene
Conditions | Yield |
---|---|
Pyrolysis; Further byproducts.; | A 2% B 10% C 1% D 4% |
ethene
A
pyrene
B
fluoranthene
C
cyclopenta[c,d]pyrene
D
benzo[ghi]fluoranthene
E
acephenanthrylene
Conditions | Yield |
---|---|
With oxygen In various solvent(s) at 1356.9℃; Product distribution; reactions under var. conditions and reaction of benzene; |
cyclopentapyren-3(4H)-one
cyclopenta[c,d]pyrene
Conditions | Yield |
---|---|
With sodium tetrahydroborate; toluene-4-sulfonic acid 1.) EtOH, 2.) toluene, reflux; Yield given. Multistep reaction; | |
Multi-step reaction with 2 steps 1: NaBH4 / methanol; tetrahydrofuran 2: 65 percent / basic activated alumina / benzene View Scheme | |
Multi-step reaction with 2 steps 1: sodium borohydride / tetrahydrofuran / 2 h / Ambient temperature 2: 83 percent / paratoluenesulfonic acid / toluene / 1 h / Heating View Scheme | |
Multi-step reaction with 2 steps 1: NaBH4 2: TsOH View Scheme |
1-ethynylpyrene
cyclopenta[c,d]pyrene
Conditions | Yield |
---|---|
at 1000℃; under 0.01 Torr; |
cyclopenta[c,d]pyrene
Conditions | Yield |
---|---|
With 2,3-dicyano-5,6-dichloro-p-benzoquinone 1.) toluene, reflux, 30 min, 2.) toluene, reflux, 1 h; Yield given. Multistep reaction; |
1,3-Bis(1-chloroethenyl)pyrene
A
cyclopenta[c,d]pyrene
B
dicyclopenta[cd,mn]pyrene
Conditions | Yield |
---|---|
at 1000℃; under 0.01 Torr; Yield given. Yields of byproduct given; |
1,8-Bis-(1-chloro-vinyl)-anthracene
A
cyclopenta[c,d]pyrene
B
benzo[ghi]fluoranthene
Conditions | Yield |
---|---|
at 1000℃; | |
at 1100℃; |
naphthanthrone
A
pyrene
B
cyclopenta[c,d]pyrene
C
benzo[ghi]fluoranthene
Conditions | Yield |
---|---|
at 1100℃; under 1 Torr; | A 4 % Spectr. B 58 % Spectr. C 19 % Spectr. |
at 1100℃; under 1 Torr; Product distribution; flash vacuum thermolysis at various pressures; | A 4 % Spectr. B 58 % Spectr. C 19 % Spectr. |
benzo[c]phenanthrene-5,6-dicarboxylic acid-anhydride
A
pyrene
B
fluoranthene
C
benzo[c]phenathrene
D
cyclopenta[c,d]pyrene
E
benzo[ghi]fluoranthene
Conditions | Yield |
---|---|
at 1100℃; under 0.01 Torr; Product distribution; Mechanism; flash vacuum thermolysis at various temp.; | A 2 % Spectr. B 2 % Spectr. C 6 % Spectr. D 39 % Spectr. E 51 % Spectr. |
benzo[c]phenanthrene-5,6-dicarboxylic acid-anhydride
A
pyrene
B
benzo[c]phenathrene
C
cyclopenta[c,d]pyrene
D
benzo[ghi]fluoranthene
Conditions | Yield |
---|---|
at 1100℃; under 0.01 Torr; Further byproducts given; | A 2 % Spectr. B 6 % Spectr. C 39 % Spectr. D 51 % Spectr. |
benzo[c]phenanthrene-5,6-dicarboxylic acid-anhydride
A
fluoranthene
B
benzo[c]phenathrene
C
cyclopenta[c,d]pyrene
D
benzo[ghi]fluoranthene
Conditions | Yield |
---|---|
at 1100℃; under 0.01 Torr; Further byproducts given; | A 2 % Spectr. B 6 % Spectr. C 39 % Spectr. D 51 % Spectr. |
at 1000℃; under 0.01 Torr; | A 2 % Spectr. B 15 % Spectr. C 20 % Spectr. D 63 % Spectr. |
Benzo[j]fluoranthene
A
Benzo[k]fluoranthene
B
PERYLENE
C
cyclopenta[c,d]pyrene
D
benzo[ghi]fluoranthene
Conditions | Yield |
---|---|
at 1200℃; under 0.01 Torr; flash vacuum thermolysis; Further byproducts given; | A 15 % Chromat. B 7 % Chromat. C 7 % Chromat. D 4 % Chromat. |
Benzo[j]fluoranthene
A
Benzo[k]fluoranthene
B
PERYLENE
C
cyclopenta[c,d]pyrene
D
cyclopentacepyrylene
Conditions | Yield |
---|---|
at 1200℃; under 0.01 Torr; flash vacuum thermolysis; Further byproducts given; | A 15 % Chromat. B 7 % Chromat. C 7 % Chromat. D 6 % Chromat. |
at 1200℃; under 0.01 Torr; flash vacuum thermolysis; Further byproducts given; | A 15 % Chromat. B 13 % Chromat. C 7 % Chromat. D 6 % Chromat. |
Conditions | Yield |
---|---|
at 1050℃; Title compound not separated from byproducts; | A 10 % Spectr. B 12 % Spectr. |
at 1100℃; under 0.0750075 Torr; Pyrolysis; |
A
phenanthridine
B
Benzo[k]fluoranthene
C
PERYLENE
D
cyclopenta[c,d]pyrene
Conditions | Yield |
---|---|
With air at 900℃; Condensation; combustion; pyrolysis; PAH formation; Formation of xenobiotics; Further byproducts given. Title compound not separated from byproducts; | A 0.04 mg B 0.04 mg C 0.12 mg D 0.03 mg |
A
11H-benzo[a]carbazole
B
Benzo[k]fluoranthene
C
Tetracen
D
cyclopenta[c,d]pyrene
Conditions | Yield |
---|---|
With air at 900℃; Condensation; combustion; pyrolysis; PAH formation; Formation of xenobiotics; Further byproducts given. Title compound not separated from byproducts; | A 0.21 mg B 0.04 mg C 0.45 mg D 0.03 mg |
A
3,4-dihydrocyclopentapyrene
B
4H-Cyclopenta[def]phenanthrene
C
cyclopenta[c,d]pyrene
D
Benzo[b]chrysene
Conditions | Yield |
---|---|
With air at 600 - 900℃; Oxidation; Formation of xenobiotics; Further byproducts given; |
A
9H-fluorene
B
phenanthrene
C
benzopyrene
D
cyclopenta[c,d]pyrene
Conditions | Yield |
---|---|
With air at 1496.85℃; Oxidation; Formation of xenobiotics; |
cyclopenta[c,d]pyrene
3,4-dihydrocyclopentapyrene
Conditions | Yield |
---|---|
With hydrogen; platinum(IV) oxide In ethyl acetate for 0.166667h; | 100% |
With hydrazine hydrate; nickel In ethanol Heating; | 98% |
cyclopenta[c,d]pyrene
cyclopentapyrene-3,4-oxide
Conditions | Yield |
---|---|
With 3,3-dimethyldioxirane In acetone at 0℃; for 0.75h; | 100% |
cyclopenta[c,d]pyrene
3,4-dihydrocyclopentapyrene 3,4-oxide
Conditions | Yield |
---|---|
With 3,3-dimethyldioxirane In acetone at 20℃; for 1h; Oxidation; | 100% |
cyclopenta[c,d]pyrene
A
cyclopentapyren-3(4H)-one
B
4-nitrocyclopentapyrene
Conditions | Yield |
---|---|
With iodine; silver nitrate; sodium nitrite In acetonitrile at 0℃; for 2.16667h; | A 30% B 43% |
With iodine; silver nitrate; sodium nitrite In acetonitrile at 0℃; for 2h; | A 30% B 43% |
cyclopenta[c,d]pyrene
benzo[ghi]fluoranthene
Conditions | Yield |
---|---|
at 1150℃; under 0.5 Torr; | 9% |
cyclopenta[c,d]pyrene
cyclopentapyren-3(4H)-one
Conditions | Yield |
---|---|
With silver(I) nitrite; iodine |
Conditions | Yield |
---|---|
at 1100℃; under 0.01 Torr; | A 1 % Spectr. B 2 % Spectr. |
at 1100℃; under 0.01 Torr; Product distribution; flash vacuum thermolysis; | A 1 % Spectr. B 2 % Spectr. |
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