2-Thiophenemethylamine - CAS 27757-85-3
Catalog: |
BB019666 |
Product Name: |
2-Thiophenemethylamine |
CAS: |
27757-85-3 |
Synonyms: |
thiophen-2-ylmethanamine |
IUPAC Name: | thiophen-2-ylmethanamine |
Description: | 2-Thiophenemethylamine (CAS# 27757-85-3) is a useful research chemical. |
Molecular Weight: | 113.18 |
Molecular Formula: | C5H7NS |
Canonical SMILES: | C1=CSC(=C1)CN |
InChI: | InChI=1S/C5H7NS/c6-4-5-2-1-3-7-5/h1-3H,4,6H2 |
InChI Key: | FKKJJPMGAWGYPN-UHFFFAOYSA-N |
Boiling Point: | 95-99 °C (28 mmHg) |
Purity: | 98 % |
Density: | 1.103 g/cm3 |
Appearance: | Clear yellow liquid |
Storage: | Keep in a cool, dry, dark location in a tightly sealed container or cylinder. Keep away from incompatible materials, ignition sources and untrained individuals. Secure and label area. Protect containers/cylinders from physical damage. |
MDL: | MFCD00005460 |
LogP: | 1.90710 |
GHS Hazard Statement: | H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation] |
Precautionary Statement: | P260, P264, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P405, and P501 |
Signal Word: | Danger |
Publication Number | Title | Priority Date |
CN-113502491-A | Electrochemical preparation method of Tioxazafen and atrareum intermediate | 20210725 |
CN-113264895-A | Synthetic method for preparing benzoxazole compound from catechol compound and amine compound | 20210606 |
CN-113264896-A | Synthetic method for preparing benzoxazole compound by oxidizing catechol compound with oxygen | 20210606 |
CN-113200967-A | Indole benzoquinone compound, preparation method and application thereof | 20210507 |
CN-113193121-A | Interface dipolar molecule modification-based perovskite solar cell and preparation method thereof | 20210408 |
PMID | Publication Date | Title | Journal |
21705267 | 20110901 | Synthesis, spectral characterization, solution equilibria, in vitro antibacterial and cytotoxic activities of Cu(II), Ni(II), Mn(II), Co(II) and Zn(II) complexes with Schiff base derived from 5-bromosalicylaldehyde and 2-aminomethylthiophene | Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy |
18024134 | 20080101 | Synthesis of 4,5,6,7-tetrahydrothieno[3,2-c]pyridines and comparison with their isosteric 1,2,3,4-tetrahydroisoquinolines as inhibitors of phenylethanolamine N-methyltransferase | Bioorganic & medicinal chemistry |
18052116 | 20071227 | Amine-guanidine switch: a promising approach to improve DNA binding and antiproliferative activities | Journal of medicinal chemistry |
11828102 | 20020201 | (2-Thienylmethyl)ammonium trichlorostannate(II): a hybrid salt | Acta crystallographica. Section C, Crystal structure communications |
Complexity: | 56 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 113.02992040 |
Formal Charge: | 0 |
Heavy Atom Count: | 7 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 113.02992040 |
Rotatable Bond Count: | 1 |
Topological Polar Surface Area: | 54.3 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 0.6 |
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