(RS)-1-(2-Diphenylphosphino-1-naphthyl)isoquinoline - CAS 149245-03-4
Catalog: |
BB010386 |
Product Name: |
(RS)-1-(2-Diphenylphosphino-1-naphthyl)isoquinoline |
CAS: |
149245-03-4 |
Synonyms: |
(1-isoquinolin-1-ylnaphthalen-2-yl)-diphenylphosphane |
IUPAC Name: | (1-isoquinolin-1-ylnaphthalen-2-yl)-diphenylphosphane |
Description: | (RS)-1-(2-Diphenylphosphino-1-naphthyl)isoquinoline (CAS# 149245-03-4 ) is a useful research chemical. |
Molecular Weight: | 439.49 |
Molecular Formula: | C31H22NP |
Canonical SMILES: | C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=C(C4=CC=CC=C4C=C3)C5=NC=CC6=CC=CC=C65 |
InChI: | InChI=1S/C31H22NP/c1-3-13-25(14-4-1)33(26-15-5-2-6-16-26)29-20-19-23-11-7-9-17-27(23)30(29)31-28-18-10-8-12-24(28)21-22-32-31/h1-22H |
InChI Key: | YMJAIEYASUCCMJ-UHFFFAOYSA-N |
Boiling Point: | 588.065 °C at 760 mmHg |
Flash Point: | Not applicable |
Purity: | 95 % |
LogP: | 6.81320 |
GHS Hazard Statement: | H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation] |
Precautionary Statement: | P261, P264, P271, P273, 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 |
WO-2020117894-A1 | Isocarbostyril alkaloids and functionalization thereof | 20181205 |
EP-3699173-A1 | Gem-disubstituted pyrrolidines, piperazines, and diazepanes, and compositions and methods of making the same | 20181018 |
US-2020399200-A1 | Method for converting n,n-dialkylamide compound into ester compound using complex of fourth-period transition metal as catalyst | 20180228 |
US-10358422-B2 | Methods for enantioselective allylic alkylation of esters, lactones, and lactams with unactivated allylic alcohols | 20171101 |
US-2019135754-A1 | Methods for enantioselective allylic alkylation of esters, lactones, and lactams with unactivated allylic alcohols | 20171101 |
PMID | Publication Date | Title | Journal |
19907787 | 20091207 | Expedient synthesis of 3-hydroxyisoquinolines and 2-hydroxy-1,4-naphthoquinones via one-pot aryne acyl-alkylation/condensation | Organic & biomolecular chemistry |
19309078 | 20090415 | Controlling axial conformation in 2-arylpyridines and 1-arylisoquinolines: application to the asymmetric synthesis of QUINAP by dynamic thermodynamic resolution | Journal of the American Chemical Society |
16557623 | 20060524 | Practical highly enantioselective synthesis of propargylamines through a copper-catalyzed one-pot three-component condensation reaction | Chemistry (Weinheim an der Bergstrasse, Germany) |
16381588 | 20060105 | Enantioselective addition of terminal alkynes to isolated isoquinoline iminiums | Organic letters |
15540267 | 20041203 | In quest of factors that control the enantioselective catalytic Markovnikov hydroboration/oxidation of vinylarenes | Chemistry (Weinheim an der Bergstrasse, Germany) |
Complexity: | 590 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 439.148986704 |
Formal Charge: | 0 |
Heavy Atom Count: | 33 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 439.148986704 |
Rotatable Bond Count: | 4 |
Topological Polar Surface Area: | 12.9 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 7.7 |
Online Inquiry
Customer Support
Customer Centered
Related Functional Groups
Quinoline/Isoquinoline
Customers Also Viewed
INDUSTRY LEADERS TRUST OUR PRODUCTS