Cyclopropylbenzene - CAS 873-49-4
Catalog: |
BB038393 |
Product Name: |
Cyclopropylbenzene |
CAS: |
873-49-4 |
Synonyms: |
cyclopropylbenzene |
IUPAC Name: | cyclopropylbenzene |
Description: | Cyclopropylbenzene (CAS# 873-49-4) is a useful research chemical. |
Molecular Weight: | 118.18 |
Molecular Formula: | C9H10 |
Canonical SMILES: | C1CC1C2=CC=CC=C2 |
InChI: | InChI=1S/C9H10/c1-2-4-8(5-3-1)9-6-7-9/h1-5,9H,6-7H2 |
InChI Key: | VFSFCYAQBIPUSL-UHFFFAOYSA-N |
Boiling Point: | 173.6 °C |
Density: | 0.94 g/cm3 |
MDL: | MFCD00001275 |
LogP: | 2.56400 |
GHS Hazard Statement: | H226 (100%): Flammable liquid and vapor [Warning Flammable liquids] |
Precautionary Statement: | P210, P233, P240, P241, P242, P243, P280, P303+P361+P353, P370+P378, P403+P235, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
US-2021275683-A1 | Nectin-4 antibody conjugates and uses thereof | 20200221 |
WO-2021168274-A1 | Nectin-4 antibody conjugates and uses thereof | 20200221 |
CN-110862292-A | Preparation method of 1-aryl-1, 2-dibromoethane | 20191119 |
CN-110862292-B | Preparation method of 1-aryl-1, 2-dibromoethane | 20191119 |
WO-2021090863-A1 | Laminate body that includes temporary adhesive film; temporary adhesive composition; laminate body manufacturing method; and semiconductor element manufacturing method | 20191107 |
PMID | Publication Date | Title | Journal |
22818040 | 20120901 | Synthesis and biological evaluation of novel C-indolylxylosides as sodium-dependent glucose co-transporter 2 inhibitors | European journal of medicinal chemistry |
21917466 | 20111015 | Synthesis and anticonvulsant activity of new N-Mannich bases derived from 5-cyclopropyl-5-phenyl- and 5-cyclopropyl-5-(4-chlorophenyl)-imidazolidine-2,4-diones | Bioorganic & medicinal chemistry |
21737272 | 20110801 | Identification of MK-5710 ((8aS)-8a-methyl-1,3-dioxo-2-[(1S,2R)-2-phenylcyclopropyl]-N-(1-phenyl-1H-pyrazol-5-yl)hexahydroimid azo[1,5-a]pyrazine-7(1H)-carboxamide), a potent smoothened antagonist for use in Hedgehog pathway dependent malignancies, part 1 | Bioorganic & medicinal chemistry letters |
21521154 | 20110701 | The design and application of target-focused compound libraries | Combinatorial chemistry & high throughput screening |
21469172 | 20110401 | Synthesis and anticonvulsant activity of new n-mannich bases derived from 5-cyclopropyl-5-phenyl-hydantoins | Archiv der Pharmazie |
Complexity: | 86.2 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 118.078250319 |
Formal Charge: | 0 |
Heavy Atom Count: | 9 |
Hydrogen Bond Acceptor Count: | 0 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 118.078250319 |
Rotatable Bond Count: | 1 |
Topological Polar Surface Area: | 0 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 3.3 |
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