Morpholine Hydrochloride - CAS 10024-89-2
Catalog: |
BB000145 |
Product Name: |
Morpholine Hydrochloride |
CAS: |
10024-89-2 |
Synonyms: |
morpholine;hydrochloride; morpholine;hydrochloride |
IUPAC Name: | morpholine;hydrochloride |
Description: | Morpholine Hydrochloride (CAS# 10024-89-2) is a useful research chemical. |
Molecular Weight: | 123.58 |
Molecular Formula: | C4H10ClNO |
Canonical SMILES: | C1COCCN1.Cl |
InChI: | InChI=1S/C4H9NO.ClH/c1-3-6-4-2-5-1;/h5H,1-4H2;1H |
InChI Key: | JXYZHMPRERWTPM-UHFFFAOYSA-N |
Boiling Point: | 106.4 °C at 760 mmHg |
Melting Point: | 179 °C |
Purity: | > 98.0 % (T) |
Density: | 0.83 g/cm3 |
Appearance: | White to light yellow powder to crystal |
Storage: | Store under inert gas |
MDL: | MFCD00035287 |
LogP: | 0.73700 |
GHS Hazard Statement: | H312 (97.67%): Harmful in contact with skin [Warning Acute toxicity, dermal] |
Precautionary Statement: | P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P322, P332+P313, P337+P313, P362, P363, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-113248359-A | Method for producing methacrolein | 20210508 |
CN-113072518-A | Dibenzo azepine derivative and preparation method thereof | 20210406 |
CN-112812041-A | Cyclohexylbiguanide hydrochloride and preparation method thereof | 20210201 |
CN-212549198-U | Mixing device for morpholine production | 20200603 |
CN-111499619-A | Medicine for treating hepatic fibrosis and preparation method thereof | 20200520 |
PMID | Publication Date | Title | Journal |
27101894 | 20160601 | Click-based synthesis and antitubercular evaluation of novel dibenzo[b,d]thiophene-1,2,3-triazoles with piperidine, piperazine, morpholine and thiomorpholine appendages | Bioorganic & medicinal chemistry letters |
23841542 | 20131101 | Copper(I) (pseudo)halide complexes with neocuproine and aminomethylphosphines derived from morpholine and thiomorpholine - in vitro cytotoxic and antimicrobial activity and the interactions with DNA and serum albumins | Chemical biology & drug design |
22746995 | 20120726 | A mechanistic and kinetic study on the decomposition of morpholine | The journal of physical chemistry. A |
22677312 | 20120715 | Haloenol pyranones and morpholinones as antineoplastic agents of prostate cancer | Bioorganic & medicinal chemistry letters |
22490555 | 20120701 | Touch responsiveness in zebrafish requires voltage-gated calcium channel 2.1b | Journal of neurophysiology |
Complexity: | 34.5 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 2 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 123.0450916 |
Formal Charge: | 0 |
Heavy Atom Count: | 7 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 2 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 123.0450916 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 21.3 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
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Morpholines/Thiomorpholines
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