(-)-Diisopropyl D-Tartrate - CAS 62961-64-2
Catalog: |
BB031901 |
Product Name: |
(-)-Diisopropyl D-Tartrate |
CAS: |
62961-64-2 |
Synonyms: |
(2S,3S)-2,3-dihydroxybutanedioic acid dipropan-2-yl ester; dipropan-2-yl (2S,3S)-2,3-dihydroxybutanedioate |
IUPAC Name: | dipropan-2-yl (2S,3S)-2,3-dihydroxybutanedioate |
Description: | (-)-Diisopropyl D-Tartrate (CAS# 62961-64-2) is a reagent for kinetic resolution of racemic allylic alcohols and α-furfuryl amides by enantioselective epoxidation. |
Molecular Weight: | 234.25 |
Molecular Formula: | C10H18O6 |
Canonical SMILES: | CC(C)OC(=O)C(C(C(=O)OC(C)C)O)O |
InChI: | InChI=1S/C10H18O6/c1-5(2)15-9(13)7(11)8(12)10(14)16-6(3)4/h5-8,11-12H,1-4H3/t7-,8-/m0/s1 |
InChI Key: | XEBCWEDRGPSHQH-YUMQZZPRSA-N |
Boiling Point: | 275 °C / 760 mmHg |
Flash Point: | 110 °C(230 °F) |
Purity: | ≥ 98 %, ≥ 95 % e.e. |
Density: | 1.117 g/mL |
Appearance: | Clear colourless liquid |
Storage: | Room temperature. |
MDL: | MFCD00008876 |
LogP: | -0.38860 |
Refractive Index: | 1.44 |
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-112592326-A | Enantioselective synthesis method of chiral (6Z,9Z) -3, 4-epoxy octadecadiene | 20201222 |
CN-112604659-A | Chiral ligand exchange type COF @ MOF/L composite material and preparation method thereof | 20201127 |
CN-112604714-A | COF @ MOF/M/L composite material and preparation method thereof | 20201127 |
CN-111440155-A | Chrysamide B derivative with anti-tumor activity and preparation and application thereof | 20200318 |
CN-111303080-A | Synthesis method of gypsy moth sex pheromone | 20200312 |
PMID | Publication Date | Title | Journal |
19580294 | 20090821 | Synthesis of (S)-imperanene by using allylic substitution | The Journal of organic chemistry |
15909353 | 20050601 | Quantum chemical study on asymmetric allylation of benzaldehyde in the presence of chiral allylboronate | Journal of Zhejiang University. Science. B |
Complexity: | 222 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 2 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 234.11033829 |
Formal Charge: | 0 |
Heavy Atom Count: | 16 |
Hydrogen Bond Acceptor Count: | 6 |
Hydrogen Bond Donor Count: | 2 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 234.11033829 |
Rotatable Bond Count: | 7 |
Topological Polar Surface Area: | 93.1 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 0.6 |
Online Inquiry
Customer Support
Customer Centered
Related Functional Groups
Carbonyl Compounds
Customers Also Viewed
INDUSTRY LEADERS TRUST OUR PRODUCTS