3,6-Diphenyl(1,2,4)triazolo(3,4-b)(1,3,4)oxadiazole

Modify Date: 2025-10-01 19:35:59

3,6-Diphenyl(1,2,4)triazolo(3,4-b)(1,3,4)oxadiazole Structure
3,6-Diphenyl(1,2,4)triazolo(3,4-b)(1,3,4)oxadiazole structure
Common Name 3,6-Diphenyl(1,2,4)triazolo(3,4-b)(1,3,4)oxadiazole
CAS Number 32550-72-4 Molecular Weight 262.26600
Density 1.36g/cm3 Boiling Point N/A
Molecular Formula C15H10N4O Melting Point N/A
MSDS N/A Flash Point N/A

 Names

Name 3,6-diphenyl-[1,2,4]triazolo[3,4-b][1,3,4]oxadiazole
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.36g/cm3
Molecular Formula C15H10N4O
Molecular Weight 262.26600
Exact Mass 262.08500
PSA 56.22000
LogP 3.05130
Index of Refraction 1.724
InChIKey SHKHLSSPOZSELN-UHFFFAOYSA-N
SMILES c1ccc(-c2nn3c(-c4ccccc4)nnc3o2)cc1

 Safety Information

HS Code 2934999090

 Synthetic Route

 Customs

HS Code 2934999090
Summary 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Bioassay

View more

Name: QFRET-based biochemical primary high throughput screening assay to identify exosite i...
Source: The Scripps Research Institute Molecular Screening Center
Target: disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id: ADAM17_INH_QFRET_1536_1X%INH PRUN
Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN
Name: qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
Source: NCGC
Target: TDP1 protein [Homo sapiens]
External Id: TDP1100
Name: qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
Source: NCGC
Target: TDP1 protein [Homo sapiens]
External Id: TDP1101
Name: Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas...
Source: Broad Institute
Target: N/A
External Id: 2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2
Name: Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
Source: Broad Institute
Target: FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id: 2147-01_Inhibitor_SinglePoint_HTS_Activity
Name: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
Source: Broad Institute
Target: N/A
External Id: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
Name: Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste...
Source: Broad Institute
Target: N/A
External Id: 7124-01_Inhibitor_SinglePoint_HTS_Activity
Name: qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima...
Source: NCGC
Target: apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id: AMA1100
Name: Fluorescence polarization-based biochemical high throughput primary assay to identify...
Source: The Scripps Research Institute Molecular Screening Center
Target: abhydrolase domain-containing protein 4 isoform 1 [Mus musculus]
External Id: ABHD4_INH_FP_1536_1X%INH PRUN
Total 80, Current Page 1 of 8
1
2
3
4
5

 Synonyms

Diphenyl-2,4 oxa-1 tetraza-3,3a,5,6 pentalene
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.