40724-67-2

Name	(1S)-(+)-ketopinic acid
Synonyms	Ketopinicacid (S)-(+)-KETOPINIC ACID (S)-(+)-Ketopinic acid (1S)-(+)-ketopinic acid (1S)-(+)-KETOPINIC ACID (1S,4R)-2-Oxobornane-10-oic acid rac-(1S,4R)-2-Oxobornane-10-oic acid 7,7-dimethyl-2-oxobicyclo[2.2.1]heptane-1-carboxylic acid (1S,4R)-7,7-Dimethyl-2-oxobicyclo[2.2.1]-1-carboxylic acid (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 (1S,4R)-7,7-dimethyl-2-oxobicyclo[2.2.1]heptane-1-carboxylic acid
CAS	40724-67-2
InChI	InChI=1/C10H14O3/c1-9(2)6-3-4-10(9,8(12)13)7(11)5-6/h6H,3-5H2,1-2H3,(H,12,13)/t6-,10+/m1/s1

Molecular Formula	C10H14O3
Molar Mass	182.22
Density	1.238±0.06 g/cm3(Predicted)
Melting Point	237-239°C(lit.)
Boling Point	313.3±25.0 °C(Predicted)
Specific Rotation(α)	58 º (C=1 IN CHLOROFORM)
Flash Point	157.5°C
Vapor Presure	0.000109mmHg at 25°C
BRN	4180005
pKa	3.67±0.40(Predicted)
Storage Condition	Sealed in dry,Room Temperature
Refractive Index	25.5 ° (C=0.65, MeOH
MDL	MFCD00168053
Use	It is used to prepare a new chiral oxazolidinone adjuvant and a keto pinic acid-derived polymer, which can be used for the de-racemization of amines. Raw materials for the synthesis of pure chiral 2,10-camphane diol. It was used to generate chiral Schiff base precursors for the preparation of diethyl (S)-α-amino-α-alkyl phosphonates.

Hazard Symbols	Xi - Irritant
Risk Codes	36/37/38 - Irritating to eyes, respiratory system and skin.
Safety Description	S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing.
WGK Germany	3

Use	(S)-( )-ketopinic acid is a useful reactant that can be used to prepare alkenyl nitriles Electrophiles are used for covalent protein labeling.

Last Update：2024-04-09 15:16:39

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40724-67-2

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