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2-Azabicyclo[3.2.1]octan-3-one, 2-hydroxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74222-01-8

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74222-01-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74222-01-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,2,2 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 74222-01:
(7*7)+(6*4)+(5*2)+(4*2)+(3*2)+(2*0)+(1*1)=98
98 % 10 = 8
So 74222-01-8 is a valid CAS Registry Number.

74222-01-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-hydroxy-2-azabicyclo[3.2.1]octan-3-one

1.2 Other means of identification

Product number -
Other names -

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:74222-01-8 SDS

74222-01-8Upstream product

74222-01-8Downstream Products

74222-01-8Relevant academic research and scientific papers

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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