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4576-48-1

NORCAMPHOR OXIME, also known as 2-norbornanone oxime, is an organic compound derived from camphor. It is a colorless to pale yellow liquid with a molecular formula of C7H11NO and a molecular weight of 125.17 g/mol. This chemical is primarily used as a synthetic intermediate in the production of various pharmaceuticals, agrochemicals, and other specialty chemicals. NORCAMPHOR OXIME is known for its unique properties, such as its ability to form stable crystalline structures and its reactivity in various chemical reactions. It is also used in the synthesis of chiral auxiliaries and ligands for asymmetric catalysis. Due to its potential applications in the pharmaceutical industry, NORCAMPHOR OXIME has gained significant attention in recent years, and research is ongoing to explore its potential uses and optimize its synthesis methods.

4576-48-1

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4576-48-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4576-48-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,7 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4576-48:
(6*4)+(5*5)+(4*7)+(3*6)+(2*4)+(1*8)=111
111 % 10 = 1
So 4576-48-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H11NO/c9-8-7-4-5-1-2-6(7)3-5/h5-6,9H,1-4H2/b8-7+

4576-48-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(3-bicyclo[2.2.1]heptanylidene)hydroxylamine

1.2 Other means of identification

Product number -
Other names Bicyclo<2.2.1>heptan-2-on-oxim

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4576-48-1 SDS

4576-48-1Upstream product

4576-48-1Relevant articles and documents

Novel Intramolecular Photorearrangement of Nitronate Anions

Yamada, Kazutoshi,Tanaka, Seiji,Naruchi, Kiyoshi,Yamamoto, Makoto

, p. 5283 - 5289 (2007/10/02)

The photochemistry of alkanenitronate anions is described.Irradiation of the alkanenitronate anions leads to hydroxamic acids by oxygen photorearrangement via ?-?* triplet excited states.The stoichiometry of reaction, anion structure and selectivity of migration, the nature of the excited state, the quantum yield of reaction, rehybridization on excitation, and the base dependency are discussed.From the results of a detailed structural study of 19 products it was found that this photorearrangement is a highly regio- and stereospecific reaction.

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