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622-32-2

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622-32-2 Usage

General Description

SYN-BENZALDEHYDE OXIME, also known as benzaldoxime, is a chemical compound that is commonly used as a building block in the synthesis of various organic compounds. It is used as a protecting group for aldehydes and ketones in organic synthesis, serving as a versatile reagent for the formation of oximes. It is often utilized in the pharmaceutical and chemical industries for the production of various intermediates and fine chemicals. SYN-BENZALDEHYDE OXIME is a versatile and valuable compound for the synthesis of a wide range of organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 622-32-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 622-32:
(5*6)+(4*2)+(3*2)+(2*3)+(1*2)=52
52 % 10 = 2
So 622-32-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H7NO/c9-8-6-7-4-2-1-3-5-7/h1-6,9H/b8-6-

622-32-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-Benzaldehyde oxime

1.2 Other means of identification

Product number -
Other names Benzaldehyde, oxime, (Z)-

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:622-32-2 SDS

622-32-2Relevant articles and documents

Direct Synthesis of Nitrones via Transition-Metal-Free Ring-Opening of N -Tosylaziridines with the Nitrogen Atom of Various (E)-Aldoximes and (E)-Ketoximes

Chang, Honghong,Gao, Wenchao,Li, Xing,Tian, Xiuping,Wei, Wenlong,Yan, Wenjing,Zhang, Rui

, p. 4043 - 4057 (2019)

The KOH-, K 2 CO 3 -, or Et 3 N-catalyzed ring-opening reaction of N -tosylaziridines using the nitrogen atom of a series of (E)-aldoximes and (E)-ketoximes as a nucleophilic atom instead of an oxygen atom was developed to construct various nitrones under mild reaction conditions. Diverse (E)-aldoximes and (E)-ketoximes were demonstrated to be compatible with this reaction and the products of O -ring-opening reactions were not detected for most examples.

Visible-light mediated stereospecific C(sp2)-H difluoroalkylation of (Z)-aldoximes

Chen, Hua,Deng, Hongmei,Gong, Haiying,Hao, Jian,Li, Mingjie,Peng, Yi,Wan, Wen,Wang, Qian,Zhang, Yifang

supporting information, p. 7867 - 7874 (2021/09/28)

A visible light mediated stereospecific C(sp2)-H difluoroalkylation of (Z)-aldoximes to (E)-difluoroalkylated ketoximes has been described. In this reaction, (hetero)-aromatic and aliphatic difluoroalkylated ketoximes could be obtained with the retention of the configuration of the starting aldoximes. A preliminary mechanism study showed that a difluoromethyl radicalviaan SET pathway was involved.

Visible-Light-Mediated Strategies for the Preparation of Oxime Ethers Derived from O-H Insertions of Oximes into Aryldiazoacetates

Duarte, Marcelo,Jurberg, Igor D.,Le?o, Luiz Paulo M. O.,Saito, Felipe A.,Stivanin, Mateus L.

supporting information, p. 17528 - 17532 (2021/12/02)

Two visible-light-mediated O-H insertion protocols involving oximes and aryldiazoacetates leading to different products depending on the solvent employed are reported. In DCM, direct O-H insertion takes place. In THF, there is the additional incorporation of the ring-opened form of this solvent into the structure of the product. These metal-free protocols are mild and tolerant to air and moisture. The preparation of an acaricide has been developed as an example of synthetic application.

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