C₇H₁₀N₄O

Base Information

Chemical Name:C₇H₁₀N₄O
CAS No.:1315552-06-7
Molecular Formula:C₇H₁₀N₄O
Molecular Weight:166.183
Hs Code.:

C<sub>7</sub>H<sub>10</sub>N<sub>4</sub>O

Synonyms:

Suppliers and Price of C₇H₁₀N₄O

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

TRC
(2R,3R,3aS,4S,6aS)-3-Azidohexahydro-2,4-methano-4H-furo[3,2-b]pyrrole
1mg
$ 675.00

Medical Isotopes, Inc.
(2R,3R,3aS,4S,6aS)-3-Azidohexahydro-2,4-methano-4H-furo[3,2-β]pyrrole
1 mg
$ 1115.00

Total 3 raw suppliers

Chemical Property of C₇H₁₀N₄O

Chemical Property:

Purity/Quality:

95%+ or 98%+ ^*data from raw suppliers

(2R,3R,3aS,4S,6aS)-3-Azidohexahydro-2,4-methano-4H-furo[3,2-b]pyrrole ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Uses (2R,3R,3aS,4S,6aS)-3-Azidohexahydro-2,4-methano-4H-furo[3,2-b]pyrrole is an intermediate in the synthesis of Loline (I707255), an alkaloid isolated from fungal endophytes, an endosymbiont that lives within a plant.

Technology Process of C₇H₁₀N₄O

There total 4 articles about C₇H₁₀N₄O 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: 90.0%

: 1315552-05-6
C₇H₁₁ClN₄O

: 1315552-06-7
C₇H₁₀N₄O

Guidance literature:: With potassium carbonate; In methanol; at 150 ℃; for 0.166667h; Inert atmosphere; Microwave irradiation;
DOI:10.1038/nchem.1072

Reference yield:

: C₁₅H₁₇NO₅S

: 1315552-06-7
C₇H₁₀N₄O

Guidance literature:: Multi-step reaction with 4 steps

1: lithium azide; water / N,N-dimethyl-formamide / 2.5 h / 130 °C / Inert atmosphere

2: bromine / 0 h / 12 °C / Inert atmosphere; Darkness

3: lithium chloride / N,N-dimethyl-formamide / 6 h / 105 °C / Inert atmosphere

4: potassium carbonate / methanol / 0.17 h / 150 °C / Inert atmosphere; Microwave irradiation

With lithium azide; water; bromine; potassium carbonate; lithium chloride; In methanol; N,N-dimethyl-formamide;
DOI:10.1038/nchem.1072

Reference yield:

: C₁₅H₁₈N₄O₃

: 1315552-06-7
C₇H₁₀N₄O

Guidance literature:: Multi-step reaction with 3 steps

1: bromine / 0 h / 12 °C / Inert atmosphere; Darkness

2: lithium chloride / N,N-dimethyl-formamide / 6 h / 105 °C / Inert atmosphere

3: potassium carbonate / methanol / 0.17 h / 150 °C / Inert atmosphere; Microwave irradiation

With bromine; potassium carbonate; lithium chloride; In methanol; N,N-dimethyl-formamide;
DOI:10.1038/nchem.1072