D-Prolinol - CAS 68832-13-3
Catalog: |
BB033638 |
Product Name: |
D-Prolinol |
CAS: |
68832-13-3 |
Synonyms: |
(R)-2-Hydroxymethyl-pyrrolidine; (R)-2-Pyrrolidinemethanol; (R)-(−)-2-Pyrrolidinemethanol |
IUPAC Name: | [(2R)-pyrrolidin-2-yl]methanol |
Description: | A reagent used for asymmetric synthesis. |
Molecular Weight: | 101.2 |
Molecular Formula: | C5H11NO |
Canonical SMILES: | C1CC(NC1)CO |
InChI: | InChI=1S/C5H11NO/c7-4-5-2-1-3-6-5/h5-7H,1-4H2/t5-/m1/s1 |
InChI Key: | HVVNJUAVDAZWCB-RXMQYKEDSA-N |
Boiling Point: | 74-76 °C at 2 mmHg |
Purity: | > 95 % by HPLC |
Density: | 1.025 g/mL |
Appearance: | Colorless transparent or pale yellow liquid |
Storage: | Store at 2-8 °C |
MDL: | MFCD00064321 |
LogP: | 0.05950 |
GHS Hazard Statement: | H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation] |
Precautionary Statement: | P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-112979532-A | Phthalimide compound, preparation method and application | 20210520 |
CN-112979532-B | Phthalimide compound, preparation method and application | 20210520 |
CN-112812101-A | Preparation method of avanafil impurity | 20210119 |
CN-112430237-A | Desulfurizing agent containing phthalocyanine double activity, preparation method and application thereof | 20201211 |
CN-111484484-A | 2, 4-diaryl aminopyrimidine derivative containing aromatic heterocycle and preparation and application thereof | 20200413 |
PMID | Publication Date | Title | Journal |
22585353 | 20120814 | Efficient proline and prolinol ether mediated 3-component synthesis of 3- and 3,4-substituted chromenone derivatives | Organic & biomolecular chemistry |
22434659 | 20120416 | Asymmetric Michael addition of N-boc-protected oxindoles to nitroalkenes catalyzed by a chiral secondary amine | Chemistry (Weinheim an der Bergstrasse, Germany) |
22374840 | 20120319 | Unifying metal- and organocatalysis for asymmetric oxidative iminium activation: a relay catalytic system enabling the combined allylic oxidation of alcohols and prolinol ether catalyzed iminium reactions | Chemistry (Weinheim an der Bergstrasse, Germany) |
22224938 | 20120120 | Relative tendency of carbonyl compounds to form enamines | Organic letters |
21552582 | 20110621 | Asymmetric alkynylation of aldehydes with propiolates without high reagent loading and any additives | Organic & biomolecular chemistry |
Complexity: | 56 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 1 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 101.084063974 |
Formal Charge: | 0 |
Heavy Atom Count: | 7 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 2 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 101.084063974 |
Rotatable Bond Count: | 1 |
Topological Polar Surface Area: | 32.3 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | -0.3 |
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