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829-08-3

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829-08-3 Usage

General Description

(1Z)-2-hydroxy-2-methyl-1-phenylpropan-1-one oxime is a chemical compound with the molecular formula C10H13NO2. It is an oxime derivative of 2-hydroxy-2-methyl-1-phenylpropan-1-one, with the oxime group (-NOH) attached to the carbonyl carbon of the ketone. (1Z)-2-hydroxy-2-methyl-1-phenylpropan-1-one oxime has potential applications in organic synthesis and medicinal chemistry. It can be used as a reagent in the preparation of various derivatives and can also serve as a building block in the synthesis of pharmaceutical compounds. Additionally, oximes have been studied for their potential antioxidant and neuroprotective properties, making (1Z)-2-hydroxy-2-methyl-1-phenylpropan-1-one oxime a potentially valuable compound in the field of pharmaceutical research.

Check Digit Verification of cas no

The CAS Registry Mumber 829-08-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,2 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 829-08:
(5*8)+(4*2)+(3*9)+(2*0)+(1*8)=83
83 % 10 = 3
So 829-08-3 is a valid CAS Registry Number.

829-08-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (1Z)-1-hydroxyimino-2-methyl-1-phenylpropan-2-ol

1.2 Other means of identification

Product number -
Other names 1-Hydroximino-2-methyl-1-phenyl-propan-2-ol

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:829-08-3 SDS

829-08-3Downstream Products

829-08-3Relevant articles and documents

Copper-Catalyzed Unstrained C-C Single Bond Cleavage of Acyclic Oxime Acetates Using Air: An Internal Oxidant-Triggered Strategy toward Nitriles and Ketones

Zhu, Chuanle,Chen, Fulin,Liu, Chi,Zeng, Hao,Yang, Zhiyi,Wu, Wanqing,Jiang, Huanfeng

, p. 14713 - 14722 (2018/12/14)

A copper-catalyzed aerobic oxidative C-C single bond cleavage of acyclic unstrained oxime acetates is reported, providing various aryl nitriles and ketones in good yields. Mechanistic studies indicate a radical procedure is involved in this transformation, and the oxygen atom in the ketone products is originated from O2 in the air. Oxime acetates as an internal oxidant have been proved to be an initiator, which may promote the discovery of novel protocol for C-C bond cleavage and dioxygen activation.

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