2-Methyloxazole - CAS 23012-10-4
Catalog: |
BB017858 |
Product Name: |
2-Methyloxazole |
CAS: |
23012-10-4 |
Synonyms: |
2-methyloxazole; 2-methyl-1,3-oxazole |
IUPAC Name: | 2-methyl-1,3-oxazole |
Description: | 2-Methyloxazole (CAS# 23012-10-4) is a useful research chemical. |
Molecular Weight: | 83.09 |
Molecular Formula: | C4H5NO |
Canonical SMILES: | CC1=NC=CO1 |
InChI: | InChI=1S/C4H5NO/c1-4-5-2-3-6-4/h2-3H,1H3 |
InChI Key: | ZCHCHJQEWYIJDQ-UHFFFAOYSA-N |
Boiling Point: | 82.277 °C at 760 mmHg |
Density: | 1.017 g/cm3 |
Appearance: | Brown liquid |
LogP: | 0.98300 |
GHS Hazard Statement: | H226 (100%): Flammable liquid and vapor [Warning Flammable liquids] |
Precautionary Statement: | P210, P233, P240, P241, P242, P243, P280, P303+P361+P353, P305+P351+P338, P310, P370+P378, P403+P235, and P501 |
Signal Word: | Danger |
Publication Number | Title | Priority Date |
CN-113428987-A | Method for removing multiple antibiotics and heavy metals in sewage | 20210709 |
CN-112973798-A | Photocatalytic material and preparation method and application thereof | 20210210 |
CN-112812998-A | New strain for degrading sulfamethoxazole and application thereof | 20210112 |
CN-112675910-A | Amyloid fiber ferric hydroxide heterogeneous Fenton catalyst and preparation method and application thereof | 20210111 |
CN-111560026-A | High-optical-stability cell membrane fluorescent marker and preparation method and application thereof | 20200511 |
PMID | Publication Date | Title | Journal |
20500830 | 20100525 | Expansion of ribosomally produced natural products: a nitrile hydratase- and Nif11-related precursor family | BMC biology |
20725629 | 20100524 | 'One ring to bind them all'-part I: the efficiency of the macrocyclic scaffold for g-quadruplex DNA recognition | Journal of nucleic acids |
19809190 | 20091001 | Biosynthesis of indolocarbazole and goadsporin, two different heterocyclic antibiotics produced by actinomycetes | Bioscience, biotechnology, and biochemistry |
19286651 | 20090508 | Structural and functional dissection of the heterocyclic peptide cytotoxin streptolysin S | The Journal of biological chemistry |
18369502 | 20080414 | Activation of two C-H bonds of NHC N-methyl groups on triosmium and triruthenium carbonyl clusters | Dalton transactions (Cambridge, England : 2003) |
Complexity: | 46.8 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 83.037113783 |
Formal Charge: | 0 |
Heavy Atom Count: | 6 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 83.037113783 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 26 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 0.7 |
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Related Functional Groups
Oxazole/Thiazole
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