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6310-87-8

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6310-87-8 Usage

General Description

The chemical compound with the systematic name "(1E)-1-[4-(dimethylamino)phenyl]ethanone oxime" is an oxime derivative of a substituted phenyl ethanone. It consists of a phenyl ring substituted with a dimethylamino group and an ester group attached to the carbon alpha to the ketone. The oxime functional group (-N=OH) is attached to the ketone group, and the compound exists in the E-configuration. (1E)-1-[4-(dimethylamino)phenyl]ethanone oxime is often used in organic synthesis and medicinal chemistry, with potential applications in pharmaceuticals and as a reagent in various chemical reactions. Its properties and potential uses make it a valuable compound in the chemical and pharmaceutical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 6310-87-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6310-87:
(6*6)+(5*3)+(4*1)+(3*0)+(2*8)+(1*7)=78
78 % 10 = 8
So 6310-87-8 is a valid CAS Registry Number.

6310-87-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (NZ)-N-[1-[4-(dimethylamino)phenyl]ethylidene]hydroxylamine

1.2 Other means of identification

Product number -
Other names 2-BUTANONE,4-(4-DIMETHYLAMINOPHENYL)-,OXIME

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:6310-87-8 SDS

6310-87-8Relevant articles and documents

Palladium-Catalyzed C-H Functionalization of Aromatic Oximes: A Strategy for the Synthesis of Isoquinolines

Zhu, Zhongzhi,Tang, Xiaodong,Li, Xianwei,Wu, Wanqing,Deng, Guohua,Jiang, Huanfeng

, p. 1401 - 1409 (2016/03/01)

An efficient strategy for synthesis of isoquinolines via Pd(II)-catalyzed cyclization reaction of oximes with vinyl azides or homocoupling of oximes is reported. Oximes could serve as a directing group and an internal oxidant in the transformation. This reaction features good functional group tolerance and provides a useful protocol for the synthesis of different kinds of isoquinolines under mild conditions. Some control experiments and 15N isotope labeling experiments were conducted for the mechanistic research. (Chemical Equation Presented).

Synthesis of β-blocking oximes. Influence of terminal amine on β-selectivity

Amlaiky,Leclerc,Decker,Schwartz

, p. 437 - 439 (2007/10/02)

Three series of oximinopropanolamine derivatives in which the terminal nitrogen has been substituted by various arylalkyl groups were synthesized. The beta-adrenergic blocking activity of the 21 compounds was determined in vitro on the guinea-pig. The structure-activity relationship is discussed.

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