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ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME

ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME structure

CAS No.: 22472-58-8

Chemical Name:: ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME

Synonyms: ISONITROSO-D-CAMPHOR;camphorquinone 3-oxime;(1R,E)-(+)-CAMPHORQUINONE 3-OXIME;(1R,E)-(+)-2,3-BORNANEDIONE 3-OXIME;ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME;ANTI-(1R)-(+)-2,3-BORNANEDIONE 3-OXIME

CBNumber:: CB4476401

Molecular Formula:: C10H15NO2

Molecular Weight:: 181.23

MDL Number:: MFCD00074848

MOL File:: 22472-58-8.mol

Last updated:2026-07-31 08:06:18

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ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME Properties

Melting point	153-156 °C(lit.)
Boiling point	276.773±7.00 °C(Press: 760.00 Torr)(predicted)
Density	1.260±0.14 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)
storage temp.	2-8°C
solubility	soluble in DCM, Ethyl Acetate, Ether, Methanol
form	Solid
pka	9.348±0.60(predicted)
color	Pale Yellow

SAFETY

Risk and Safety Statements

Safety Statements	22-24/25
WGK Germany	3

ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME price

Manufacturer	Product number	Product description	CAS number	Packaging	Price	Updated	Buy
TRC	C175005	(1R,4S)-CamphorquinoneMonooxime	22472-58-8	10g	$820	2021-12-16	Buy

Product number	Packaging	Price	Buy
C175005	10g	$820	Buy

ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME Chemical Properties,Uses,Production

Uses

(1R,4S)-Camphorquinone Monooximeis an intermediate in the synthesis of Gibornuride (G409700), an anti-diabetic drug from the group of sulfonylureas.

ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME Preparation Products And Raw materials

Raw materials

Preparation Products

ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME Suppliers

Global( 4)Suppliers

Supplier	Tel	Email	Country	ProdList	Advantage
Energy Chemical	021-58432009 400-005-6266	marketing@energy-chemical.com	China	44871	58

Supplier	Advantage
Energy Chemical	58

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ISONITROSO-D-CAMPHOR ANTI-(1R)-(+)-2,3-BORNANEDIONE 3-OXIME ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME (1R,E)-(+)-2,3-BORNANEDIONE 3-OXIME (1R,E)-(+)-CAMPHORQUINONE 3-OXIME camphorquinone 3-oxime 22472-58-8 Organic Building Blocks Oximes Chiral Building Blocks Asymmetric Synthesis Terpenes Bicyclic Monoterpenes