1-Formylpyrrolidine - CAS 3760-54-1
Catalog: |
BB023359 |
Product Name: |
1-Formylpyrrolidine |
CAS: |
3760-54-1 |
Synonyms: |
pyrrolidine-1-carbaldehyde |
IUPAC Name: | pyrrolidine-1-carbaldehyde |
Description: | 1-Formylpyrrolidine (CAS# 3760-54-1) is a useful research chemical. |
Molecular Weight: | 99.13 |
Molecular Formula: | C5H9NO |
Canonical SMILES: | C1CCN(C1)C=O |
InChI: | InChI=1S/C5H9NO/c7-5-6-3-1-2-4-6/h5H,1-4H2 |
InChI Key: | AGRIQBHIKABLPJ-UHFFFAOYSA-N |
Boiling Point: | 204.4 °C at 760 mmHg |
Density: | 1.04 g/cm3 |
Appearance: | Clear light brown liquid |
LogP: | 0.81240 |
Vapor Pressure: | 1.28 [mmHg] |
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-113117085-A | Medicine and method for preventing and treating alopecia | 20210415 |
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KR-20200096455-A | Novel pyridine derivatives having inhibition activity against SHIP2 and pharmaceutical compositions with the components | 20200803 |
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WO-2021202688-A1 | Process for preparing a cot inhibitor compound | 20200402 |
PMID | Publication Date | Title | Journal |
29635166 | 20180510 | Targeting the entrance channel of NNIBP: Discovery of diarylnicotinamide 1,4-disubstituted 1,2,3-triazoles as novel HIV-1 NNRTIs with high potency against wild-type and E138K mutant virus | European journal of medicinal chemistry |
22404301 | 20120412 | Synthesis and discovery of N-carbonylpyrrolidine- or N-sulfonylpyrrolidine-containing uracil derivatives as potent human deoxyuridine triphosphatase inhibitors | Journal of medicinal chemistry |
20198643 | 20100615 | Tyrosine hydroxylase deficiency in three Greek patients with a common ancestral mutation | Movement disorders : official journal of the Movement Disorder Society |
19132939 | 20090205 | Amide-directed alkenylation of sp(2) C-H Bonds catalyzed by a cationic Rh(I)/BIPHEP complex under mild conditions: dramatic rate acceleration by a 1-pyrrolidinecarbonyl group | Organic letters |
18355694 | 20080401 | Radiosynthesis and ex vivo evaluation of [11C]-SIB-1553A as a PET radiotracer for beta4 selective subtype nicotinic acetylcholine receptor | Nuclear medicine and biology |
Complexity: | 66.5 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 99.068413911 |
Formal Charge: | 0 |
Heavy Atom Count: | 7 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 99.068413911 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 20.3 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | -0.3 |
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