Propiolamide - CAS 7341-96-0
Catalog: |
BB034841 |
Product Name: |
Propiolamide |
CAS: |
7341-96-0 |
Synonyms: |
prop-2-ynamide |
IUPAC Name: | prop-2-ynamide |
Description: | Propiolamide (CAS# 7341-96-0) is a compound useful in organic synthesis. |
Molecular Weight: | 69.06 |
Molecular Formula: | C3H3NO |
Canonical SMILES: | C#CC(=O)N |
InChI: | InChI=1S/C3H3NO/c1-2-3(4)5/h1H,(H2,4,5) |
InChI Key: | HCJTYESURSHXNB-UHFFFAOYSA-N |
Boiling Point: | 134.6 °C at 760 mmHg |
Melting Point: | 61-62 °C |
Purity: | 95 % |
Density: | 1.102 g/cm3 |
Appearance: | Waxy yellow solid |
Storage: | -20 °C Freezer |
MDL: | MFCD04035573 |
LogP: | -0.19480 |
GHS Hazard Statement: | H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral] |
Precautionary Statement: | P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-113003738-A | Cleaning scale inhibitor and preparation method and application thereof | 20210225 |
CN-112142617-A | Method for synthesizing alpha, beta-unsaturated alkynylamide compound by oxidative carbonylation | 20201103 |
CN-112047996-A | Method for selectively modifying cysteine through propargyl sulfonium salt | 20200914 |
CN-111233617-A | Synthesis method of 1-iodoalkyne compound | 20200330 |
CN-111233872-A | Preparation method of naphtho-triazole diazepinone compound | 20200320 |
PMID | Publication Date | Title | Journal |
22606164 | 20120401 | (3β,18β,20β)-N-Eth-oxy-carbonyl-methyl-3-nitrato-11-oxoolean-12-ene-29-carboxamide methanol monosolvate | Acta crystallographica. Section E, Structure reports online |
22346914 | 20120201 | N-[2-(N-Cyclo-hexyl-carbamo-yl)propan-2-yl]-N-(2-iodo-phen-yl)prop-2-ynamide | Acta crystallographica. Section E, Structure reports online |
22220063 | 20111101 | Propargylaminyl 3α-hy-droxy-11-oxo-18β-olean-12-en-29-oate | Acta crystallographica. Section E, Structure reports online |
21627121 | 20110623 | Irreversible Nek2 kinase inhibitors with cellular activity | Journal of medicinal chemistry |
21203616 | 20110221 | A novel Zn-catalyzed hydroamination of propargylamides: a general synthesis of di- and tri-substituted imidazoles | Chemical communications (Cambridge, England) |
Complexity: | 86.3 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 69.021463719 |
Formal Charge: | 0 |
Heavy Atom Count: | 5 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 69.021463719 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 43.1 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | -0.4 |
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