2-Phenyl(1,3)oxazolo(5,4-d)pyrimidin-7-amine

Base Information

Chemical Name:2-Phenyl(1,3)oxazolo(5,4-d)pyrimidin-7-amine
CAS No.:25680-42-6
Molecular Formula:C₁₁H₈N₄O
Molecular Weight:212.211
Hs Code.:
NSC Number:137472
UNII:5J2C886J29
DSSTox Substance ID:DTXSID80180379
Nikkaji Number:J3.480.732I
Wikidata:Q83050911

Synonyms:25680-42-6;2-phenyloxazolo[5,4-d]pyrimidin-7-amine;2-Phenyl(1,3)oxazolo(5,4-d)pyrimidin-7-amine;2-phenyl-[1,3]oxazolo[5,4-d]pyrimidin-7-amine;NSC137472;2-Phenyl[1,3]oxazolo[5,4-d]pyrimidin-7-amine;5J2C886J29;NSC-137472;2-Phenyloxazolo(5,4-d)pyrimidin-7-amine;HMS564I15;NSC 137472;Maybridge1_008111;UNII-5J2C886J29;DTXSID80180379;CCG-49189;7-amino-2-phenyloxazolo[5,4-d]pyrimidine;Oxazolo[5,4-d]pyrimidin-7-amine, 2-phenyl-;2-Phenyl[1,3]oxazolo[5,4-d]pyrimidin-7-ylamine;SR-01000638661-1;BRD-K63467759-001-01-1

Suppliers and Price of 2-Phenyl(1,3)oxazolo(5,4-d)pyrimidin-7-amine

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 5 raw suppliers

Chemical Property of 2-Phenyl(1,3)oxazolo(5,4-d)pyrimidin-7-amine

Chemical Property:

Vapor Pressure:2.77E-06mmHg at 25°C
Boiling Point:389.8°C at 760 mmHg
Flash Point:189.6°C
Density:1.381g/cm³
XLogP3:1.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:1
Exact Mass:212.06981089
Heavy Atom Count:16
Complexity:244

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=NC3=C(N=CN=C3O2)N

Technology Process of 2-Phenyl(1,3)oxazolo(5,4-d)pyrimidin-7-amine

There total 7 articles about 2-Phenyl(1,3)oxazolo(5,4-d)pyrimidin-7-amine 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:

: 25680-33-5
N-(4-cyano-2-phenyl-oxazol-5-yl)-formimidic acid ethyl ester

: 25680-42-6
7-Amino-2-phenyloxazolo<5,4-d>pyrimidin

Guidance literature:: With ammonium hydroxide;
DOI:10.1246/bcsj.43.187

Reference yield:

: 5098-18-0
5-amino-2-phenyl[1,3]oxazole-4-carbonitrile

: 25680-42-6
7-Amino-2-phenyloxazolo<5,4-d>pyrimidin

Guidance literature:: Multi-step reaction with 2 steps

1: Ac₂O

2: aq. NH₃

With ammonium hydroxide; acetic anhydride;
DOI:10.1246/bcsj.43.187

Reference yield:

: 98-88-4
benzoyl chloride

: 25680-42-6
7-Amino-2-phenyloxazolo<5,4-d>pyrimidin

: C₁₈H₁₂N₄O₂

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydroxide / 0.17 h / 0 °C

1.2: 0.5 h / 20 °C

2.1: phosphoric acid

With phosphoric acid; sodium hydroxide;
DOI:10.1002/cmdc.201700137