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We produce and export 3',5'-Cyclic Adenosine Monophosphate to many courtries all the year round, the customers are all satisfied with our quality and service. Product name: Cyclic AMP CAS No.: 60-
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Cyclic AMP CAS 60-92-4 3'-5' Cyclic adenosine monophosphate CAS no 60-92-4 Adenosine 3′,5′-cyclic monophosphate Cyclic AMP IN Stock CAS 60-92-4 Cyclic AMP COA TDS price MSDS Cyclic AMP MSDS Product no. chemwill-Cyclic AMP-6
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inquiryName:Adenosine Cyclophosphate CAS:60-92-4 Grade:For chemical industry, scientific research and export Product Quality 12 years of chemical raw materials Mature operation of the industry System stability Data storage Security without vulnerabi
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inquiryCyclic AMP Basic information Product Name: Cyclic AMP Synonyms: adenosine 3',5'-phosphate monohydrate;CAMP;CAMP, ADENOSINE-3',5'-CYCLIC MONOPHOSPHATE;CYCLIC AMP;CYCLIC AMP-3',5';5’-cyclicmonophosphate;6-(6-Amino-9H
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inquiryProduct Name Adenosine Cyclophosphate Appearance White powder CAS No. 60-92-4 Grade Standard Excellent Storage Co
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inquirymethyl iodide
A
O3',O5'-methoxyphosphoryl-adenosine
B
O3',O5'-hydroxyphosphoryl-1-methyl-6,N6-didehydro-1,6-dihydro-adenosine
C
cAMP
Conditions | Yield |
---|---|
With sodium carbonate In N,N-dimethyl acetamide at 80℃; for 0.0833333h; Yields of byproduct given; | A 68.5% B n/a C n/a |
benzyl bromide
A
(4aR,6R,7R,7aS)-6-(1-Benzyl-6-imino-1,6-dihydro-purin-9-yl)-2-oxo-tetrahydro-2λ5-furo[3,2-d][1,3,2]dioxaphosphinine-2,7-diol
B
(4aR,6R,7R,7aS)-6-(1-Benzyl-6-imino-1,6-dihydro-purin-9-yl)-2-benzyloxy-2-oxo-tetrahydro-2λ5-furo[3,2-d][1,3,2]dioxaphosphinin-7-ol
C
cAMP
D
cAMP benzyl ester
Conditions | Yield |
---|---|
With sodium carbonate In N,N-dimethyl acetamide at 80℃; for 0.25h; | A n/a B 0.7% C n/a D 34% |
With sodium carbonate In N,N-dimethyl acetamide at 80℃; for 0.25h; Product distribution; other alkyl halide; var. inorganic carbonates; | A 2 % Chromat. B 5 % Chromat. C 17 % Chromat. D 74 % Chromat. |
C10H12Cl2N5O5P
cAMP
Conditions | Yield |
---|---|
With potassium hydroxide In water; acetonitrile at 0℃; Yield given; |
2-carboxy-1,N6-etheno adenosine 3',5'-cyclic phosphate
cAMP
Conditions | Yield |
---|---|
In dimethyl sulfoxide Heating; role of the 1,N6-etheno bridge in decarboxylation (without that decarboxylation did not take place at all); |
Conditions | Yield |
---|---|
In 1,4-dioxane; water Quantum yield; Rate constant; Mechanism; Irradiation; var. solvents, var. pH; | |
With Tris buffer In water-d2 at 40℃; Quantum yield; Irradiation; |
A
6-methoxy-1-hydroxymethyl-3-oxo-3H-benzopyran
B
cAMP
Conditions | Yield |
---|---|
With water In 1,4-dioxane Irradiation; |
A
6-methoxy-1-hydroxymethyl-3-oxo-3H-benzopyran
B
cAMP
Conditions | Yield |
---|---|
With HEPES buffer In methanol; water Quantum yield; photolytic cleavage; UV-irradiation; | |
In methanol; water pH=7.2; Quantum yield; UV-irradiation; |
A
6-methoxy-1-hydroxymethyl-3-oxo-3H-benzopyran
B
cAMP
Conditions | Yield |
---|---|
With HEPES buffer In methanol; water Quantum yield; photolytic cleavage; UV-irradiation; | |
In methanol; water pH=7.2; Quantum yield; UV-irradiation; |
cAMP
Conditions | Yield |
---|---|
With pyridine; tributyl-amine; dicyclohexyl-carbodiimide |
cAMP
Conditions | Yield |
---|---|
With barium dihydroxide |
equatorial-[7-(diethylamino)coumarin-4-yl]methyl adenosine cyclic 3',5'-monophosphate
cAMP
Conditions | Yield |
---|---|
In water Quantum yield; Irradiation; |
axial-[7-(diethylamino)coumarin-4-yl]methyl adenosine cyclic 3',5'-monophosphate
cAMP
Conditions | Yield |
---|---|
In water Quantum yield; Irradiation; |
[7-(carboxymethoxy)coumarin-4-yl]methyl ester of cAMP
cAMP
Conditions | Yield |
---|---|
In water Quantum yield; Irradiation; |
[7-(carboxymethoxy)coumarin-4-yl]methyl ester of cAMP
cAMP
Conditions | Yield |
---|---|
In water Quantum yield; Irradiation; |
cyclic adenosine-3',5'-monophosphate [6,7-bis(carboxymethoxy)coumarin-4-yl]methyl ester
cAMP
Conditions | Yield |
---|---|
In water Quantum yield; Irradiation; |
cyclic adenosine-3',5'-monophosphate [6,7-bis(carboxymethoxy)coumarin-4-yl]methyl ester
cAMP
Conditions | Yield |
---|---|
In water Quantum yield; Irradiation; |
equatorial-[7-(diethylamino)coumarin-4-yl]methyl adenosine cyclic 3',5'-monophosphate
A
7-(diethylamino)-4-(hydroxymethyl)-2H-chromen-2-one
B
cAMP
Conditions | Yield |
---|---|
In methanol; water pH=7.2; Quantum yield; UV-irradiation; |
axial-[7-(diethylamino)coumarin-4-yl]methyl adenosine cyclic 3',5'-monophosphate
A
7-(diethylamino)-4-(hydroxymethyl)-2H-chromen-2-one
B
cAMP
Conditions | Yield |
---|---|
In methanol; water pH=7.2; Quantum yield; UV-irradiation; |
equatorial-(coumarin-4-yl)methyl adenosine cyclic 3',5'-monophosphate
A
4-(hydroxymethyl)coumarin
B
cAMP
Conditions | Yield |
---|---|
In methanol; water pH=7.2; Quantum yield; UV-irradiation; |
axial-(coumarin-4-yl)methyl adenosine cyclic 3',5'-monophosphate
A
4-(hydroxymethyl)coumarin
B
cAMP
Conditions | Yield |
---|---|
In methanol; water pH=7.2; Quantum yield; UV-irradiation; |
equatorial-(6-methoxycoumarin-4-yl)methyl adenosine cyclic 3',5'-monophosphate
A
cAMP
Conditions | Yield |
---|---|
In methanol; water pH=7.2; Quantum yield; UV-irradiation; |
axial-(6-methoxycoumarin-4-yl)methyl adenosine cyclic 3',5'-monophosphate
A
cAMP
Conditions | Yield |
---|---|
In methanol; water pH=7.2; Quantum yield; UV-irradiation; |
A
cAMP
B
7-(dimethylamino)-4-(hydroxymethyl)-2H-chromen-2-one
Conditions | Yield |
---|---|
In methanol; water pH=7.2; Quantum yield; UV-irradiation; |
A
cAMP
B
7-(dimethylamino)-4-(hydroxymethyl)-2H-chromen-2-one
Conditions | Yield |
---|---|
In methanol; water pH=7.2; Quantum yield; UV-irradiation; |
A
cAMP
B
6,7-dimethoxy-4-(hydroxymethyl)coumarin
Conditions | Yield |
---|---|
In methanol; water pH=7.2; Quantum yield; UV-irradiation; |
axial-(6,7-dimethoxycoumarin-4-yl)methyl adenosine cyclic 3',5'-monophosphate
A
cAMP
B
6,7-dimethoxy-4-(hydroxymethyl)coumarin
Conditions | Yield |
---|---|
In methanol; water pH=7.2; Quantum yield; UV-irradiation; |
Diadenosine triphosphate
A
cAMP
B
5'-adenosine monophosphate
C
adenosine 5'-diphosphate
Conditions | Yield |
---|---|
With sodium hydroxide at 90℃; Kinetics; Product distribution; Further Variations:; pH-values; |
cAMP
Conditions | Yield |
---|---|
With calcium chloride In ethanol; water at 20℃; for 0.166667h; | 96.98% |
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 80℃; for 7h; Solvent; Reagent/catalyst; Temperature; Inert atmosphere; | 96.09% |
cAMP
adenosine 3',5'-(cyclic)phosphate monosodium salt
Conditions | Yield |
---|---|
With sodium hydroxide In water at 40℃; for 0.666667h; pH=6.6 - 6.7; Temperature; | 96% |
cAMP
Conditions | Yield |
---|---|
With calcium carbonate In water at 60℃; for 0.833333h; pH=6.7 - 6.8; Reagent/catalyst; Temperature; | 93.8% |
Conditions | Yield |
---|---|
With phosphate buffer at 25℃; for 5h; AMP deaminase from Aspergillus sp.; | 93% |
Conditions | Yield |
---|---|
With sodium hydroxide In 1,4-dioxane Ambient temperature; | 80% |
cAMP
Br-cAMP
Conditions | Yield |
---|---|
With bromine; sodium acetate In water at 20℃; for 24h; | 76% |
With bromine; sodium acetate In water at 20℃; for 25h; | 76% |
With bromine; sodium acetate In water at 20℃; for 24h; |
cAMP
Conditions | Yield |
---|---|
Stage #1: cAMP With tributyl-amine In methanol; ethanol for 1h; Reflux; Stage #2: (E)-di-tert-butyl 2-(3-(7-(diethylamino)-4-(((methylsulfonyl)oxy)methyl)-2-oxo-2H-chromen-3-yl)acrylamido)succinate In acetonitrile for 2.5h; Reflux; | 65% |
cAMP
Conditions | Yield |
---|---|
In methanol at 20℃; for 25.5h; | 57% |
Conditions | Yield |
---|---|
With silver(l) oxide In dimethyl sulfoxide; acetonitrile at 65℃; for 18h; | 52% |
4-(bromomethyl)-7-methoxycoumarin
cAMP
Conditions | Yield |
---|---|
With silver(l) oxide In dimethyl sulfoxide; acetonitrile at 60℃; for 45h; | 44% |
Conditions | Yield |
---|---|
With dmap In N,N-dimethyl-formamide at 30℃; for 18h; | 38% |
Conditions | Yield |
---|---|
With silver(l) oxide In dimethyl sulfoxide; acetonitrile at 60℃; for 45h; | A 31% B 27% |
Conditions | Yield |
---|---|
With silver(l) oxide In dimethyl sulfoxide; acetonitrile at 60℃; for 45h; | 14% |
Conditions | Yield |
---|---|
at 98℃; zeitlicher Verlauf.Hydrolysis; | |
at 100℃; zeitlicher Verlauf.Hydrolysis; |
cAMP
phosphoric acid inosine-3',5'-diyl ester
Conditions | Yield |
---|---|
With potassium nitrite; water wss.Loesung vom pH 3; |
Conditions | Yield |
---|---|
With cerium(III) chloride; water at 30℃; Rate constant; Mechanism; pH 8.0; velocity const. - var. pH's dependence; | |
With buffer pH 7; tris(3-aminopropyl)amine cobalt(III) hydroxo aqua at 25℃; relative rates of hydrolysis to the monoesters 3'-AMP and 5'-AMP; var. cobalt(III)-complexes; | |
With hydrogenchloride at 90.1℃; Rate constant; |
Conditions | Yield |
---|---|
With tributyl-amine In acetic acid at 50℃; for 0.5h; |
Conditions | Yield |
---|---|
With sodium hydroxide; silver nitrate 1.) water; 2.) DMF, rt, 3 days; Yield given. Multistep reaction; |
Conditions | Yield |
---|---|
With barium(II) iodide; sodium perchlorate; triethylamine 1.) pyridine, heating 3-4 min, then Rt, 6 d; 2.) water, methanol, ether; 3.) methanol, acetone; Multistep reaction; |
Conditions | Yield |
---|---|
With tributyl-amine In acetic acid at 50℃; for 0.5h; |
(E/Z)-crotyl bromide
cAMP
Conditions | Yield |
---|---|
With 2,6-dimethylpyridine; 1,5-Diazabicyclo[5.4.0]undec-5-ene In N,N-dimethyl-formamide at 60℃; for 5h; | 146 g |
Conditions | Yield |
---|---|
With tributyl-amine In acetic acid at 50℃; for 0.5h; |
Conditions | Yield |
---|---|
With tributyl-amine In acetic acid at 50℃; for 0.5h; |
Conditions | Yield |
---|---|
With tributyl-amine In acetic acid at 50℃; for 0.5h; |
Conditions | Yield |
---|---|
With tributyl-amine In acetic acid at 50℃; for 0.5h; |
Conditions | Yield |
---|---|
With tributyl-amine In chloroform; acetic acid at 50℃; for 0.5h; |
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