Monobutyryl cyclic AMP

Base Information

Chemical Name:Monobutyryl cyclic AMP
CAS No.:13117-60-7
Molecular Formula:C₁₄H₁₈N₅O₇P
Molecular Weight:399.3
Hs Code.:
European Community (EC) Number:251-382-2
DSSTox Substance ID:DTXSID60927103
Nikkaji Number:J77.561D
Wikidata:Q27157909
Mol file:13117-60-7.mol

Synonyms:monobutyryl cyclic AMP;monobutyryl cyclic AMP, monosodium salt;N(6)-butyryl adenosine-3',5'-cyclic monophosphate;N(6)-butyryl cyclic AMP;N(6)-monobutyryl adenosine-3',5'-cyclic monophosphate;N(6)-monobutyryl cyclic AMP

Suppliers and Price of Monobutyryl cyclic AMP

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 2 raw suppliers

Chemical Property of Monobutyryl cyclic AMP

Chemical Property:

Refractive Index:1.813
Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：167.73000
Density:1.98g/cm³
LogP:0.41200
XLogP3:-1.9
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:10
Rotatable Bond Count:4
Exact Mass:399.09438493
Heavy Atom Count:27
Complexity:627

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCC(=O)NC1=C2C(=NC=N1)N(C=N2)C3C(C4C(O3)COP(=O)(O4)O)O
Isomeric SMILES:CCCC(=O)NC1=C2C(=NC=N1)N(C=N2)[C@H]3[C@@H]([C@H]4[C@H](O3)COP(=O)(O4)O)O

Technology Process of Monobutyryl cyclic AMP

There total 6 articles about Monobutyryl cyclic AMP which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 6-N-butanoyl-adenosine-3',5'-(4-octanoyloxybenzyl)cyclophosphate

: 13117-60-7
N⁶-monobutyryl cAMP

Guidance literature:: With water; In aq. phosphate buffer; dimethyl sulfoxide; at 37 ℃; pH=7.3;
DOI:10.3390/molecules23112960

Reference yield:

: 4662-11-7
6-N-butanoyl-adenosine

: 13117-60-7
N⁶-monobutyryl cAMP

Guidance literature:: Multi-step reaction with 2 steps

1.1: 4,5-dicyano-1H-imidazole; benzyl tetrazol-5-yl sulphide / N,N-dimethyl-formamide; acetonitrile / 1 h / 20 °C / Inert atmosphere

1.2: 1 h / 20 °C / Inert atmosphere

2.1: water / dimethyl sulfoxide; aq. phosphate buffer / 37 °C / pH 7.3

With 4,5-dicyano-1H-imidazole; benzyl tetrazol-5-yl sulphide; water; In aq. phosphate buffer; dimethyl sulfoxide; N,N-dimethyl-formamide; acetonitrile;
DOI:10.3390/molecules23112960

Reference yield:

: 10457-15-5
O^2'_,O3'_,O5'-tris-trimethylsilanyl-adenosine

: 13117-60-7
N⁶-monobutyryl cAMP

Guidance literature:: Multi-step reaction with 4 steps

1.1: pyridine / tetrahydrofuran / 6 h / 20 °C

2.1: hydrogenchloride / water / 0.08 h / 20 °C

3.1: 4,5-dicyano-1H-imidazole; benzyl tetrazol-5-yl sulphide / N,N-dimethyl-formamide; acetonitrile / 1 h / 20 °C / Inert atmosphere

3.2: 1 h / 20 °C / Inert atmosphere

4.1: water / dimethyl sulfoxide; aq. phosphate buffer / 37 °C / pH 7.3

With pyridine; hydrogenchloride; 4,5-dicyano-1H-imidazole; benzyl tetrazol-5-yl sulphide; water; In tetrahydrofuran; aq. phosphate buffer; water; dimethyl sulfoxide; N,N-dimethyl-formamide; acetonitrile;
DOI:10.3390/molecules23112960