2-[3-(1H-benzoimidazol-2-yl)propyl]-1H-benzoimidazole

Modify Date: 2025-10-09 12:00:59

2-[3-(1H-benzoimidazol-2-yl)propyl]-1H-benzoimidazole Structure
2-[3-(1H-benzoimidazol-2-yl)propyl]-1H-benzoimidazole structure
Common Name 2-[3-(1H-benzoimidazol-2-yl)propyl]-1H-benzoimidazole
CAS Number 7147-66-2 Molecular Weight 276.33600
Density 1.311g/cm3 Boiling Point 630.1ºC at 760 mmHg
Molecular Formula C17H16N4 Melting Point N/A
MSDS N/A Flash Point 297.8ºC

 Names

Name 2-[3-(1H-benzimidazol-2-yl)propyl]-1H-benzimidazole

 Chemical & Physical Properties

Density 1.311g/cm3
Boiling Point 630.1ºC at 760 mmHg
Molecular Formula C17H16N4
Molecular Weight 276.33600
Flash Point 297.8ºC
Exact Mass 276.13700
PSA 57.36000
LogP 3.61450
Index of Refraction 1.747
InChIKey DKPRGKDYGLKMLF-UHFFFAOYSA-N
SMILES c1ccc2[nH]c(CCCc3nc4ccccc4[nH]3)nc2c1

 Safety Information

HS Code 2933990090

 Synthetic Route

~69%

2-[3-(1H-benzoimidazol-2-yl)propyl]-1H-benzoimidazole Structure

2-[3-(1H-benzoi...

CAS#:7147-66-2

Literature: Inamdar, Suleman M.; More, Vinod K.; Mandal, Sisir K. Tetrahedron Letters, 2013 , vol. 54, # 6 p. 579 - 583

~98%

2-[3-(1H-benzoimidazol-2-yl)propyl]-1H-benzoimidazole Structure

2-[3-(1H-benzoi...

CAS#:7147-66-2

Literature: Mukhopadhyay, Chhanda; Ghosh, Sabari; Butcher, Ray J. Arkivoc, 2010 , vol. 2010, # 9 p. 75 - 96

~%

2-[3-(1H-benzoimidazol-2-yl)propyl]-1H-benzoimidazole Structure

2-[3-(1H-benzoi...

CAS#:7147-66-2

Literature: Ried; Patschorke Justus Liebigs Annalen der Chemie, 1956 , vol. 599, p. 44,49

 Customs

HS Code 2933990090
Summary 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Bioassay

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Name: Primary cell-based high-throughput screening assay for identification of compounds th...
Source: Johns Hopkins Ion Channel Center
Target: regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id: JHICC_RGS_Act_HTS
Name: Luminescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id: OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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: uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
Source: Burnham Center for Chemical Genomics
Target: N/A
External Id: BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
Name: A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id: HMS979
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: Dicer-mediated maturation of pre-microRNA
Source: Center for Chemical Genomics, University of Michigan
Target: N/A
External Id: TargetID_659_CEMA
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