(S)-(+)-KETOPINIC ACID

(S)-(+)-KETOPINIC ACID
  • CAS No.:40724-67-2

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  1. This product is a chemical product/pharmaceutical intermediate. It is not a drug, an active pharmaceutical ingredient (API), or a pharmaceutical-grade material. It has not been granted a drug approval number or a Chemical Drug Substance Approval Notice, has not passed drug-related review and approval, and is not manufactured, tested, or released in accordance with pharmaceutical GMP.
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(S)-(+)-KETOPINIC ACID Basic information
Uses
Product Name:(S)-(+)-KETOPINIC ACID
Synonyms:(1S)-(+)-KETOPINIC ACID;(1S)-(+)-KETOPINIC ACID 97+%;(1s)-7,7-dimethyl-2-oxobicyclo[2.2.1]heptane-1-carboxylic acid;(S)-7,7-DIMETHYL-2-OXO-BICYCLO[2.2.1]HEPTANE-1-CARBOXYLIC ACID;(S)-(+)-KETOPINIC ACID;rac-(1S*,4R*)-2-Oxobornane-10-oic acid;(1S,4R)-2-Oxobornane-10-oic acid;(1S,4R)-7,7-Dimethyl-2-oxobicyclo[2.2.1]-1-carboxylic acid
CAS:40724-67-2
MF:C10H14O3
MW:182.22
EINECS:
Product Categories:Asymmetric Synthesis;Bicyclic Monoterpenes;Chiral Reagents;Biochemistry;Synthetic Organic Chemistry;Terpenes
Mol File:40724-67-2.mol
(S)-(+)-KETOPINIC ACID Chemical Properties
Melting point 237-239 °C(lit.)
alpha 58 º (C=1 IN CHLOROFORM)
Boiling point 313.3±25.0 °C(Predicted)
density 1.238±0.06 g/cm3(Predicted)
refractive index 25.5 ° (C=0.65, MeOH)
storage temp. Sealed in dry,Room Temperature
pka3.67±0.40(Predicted)
form powder to crystal
color White to Almost white
optical activity[α]23/D +58°, c = 1 in chloroform
BRN 4180005
CAS DataBase Reference40724-67-2(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
HS Code 2918300090
MSDS Information
(S)-(+)-KETOPINIC ACID Usage And Synthesis
Uses7,7-Dimethyl-2-oxobicyclo[2.2.1]heptane-1-carboxylic Acid is a useful reactant for the preparation of alkenyl nitrile electrophiles for the possible use of covalent protein labeling.
Uses(1S)-(+)-Ketopinic acid may be used to prepare:
  • Chiral phosphine-oxazoline ligands, which can used in asymmetric palladium-catalyzed Heck reaction of aryl or alkenyl triflates with cyclic alkenes.
  • A chiral imino-phosphine ligand, which can be used in palladium-catalyzed asymmetric Diels–Alder reactions to prepare six-membered carbocycles.
  • A chiral iminopyridine ligand, which can be used in copper-catalyzed Henry (nitro aldol) reaction between nitromethane and o-anisol to form the corresponding β-hydroxynitroalkane.
Uses7,7-Dimethyl-2-oxobicyclo[2.2.1]heptane-1-carboxylic Acid is a useful reactant for the preparation of alkenyl nitrile electrophiles for the possible use of covalent protein labeling.
General Description(1S)-(+)-Ketopinic acid is a chiral ketone.
(S)-(+)-KETOPINIC ACID Preparation Products And Raw materials

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