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Phenyl(4-nitrophenyl) ketone oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38032-13-2

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38032-13-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38032-13-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,0,3 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 38032-13:
(7*3)+(6*8)+(5*0)+(4*3)+(3*2)+(2*1)+(1*3)=92
92 % 10 = 2
So 38032-13-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H10N2O3/c16-14-13(10-4-2-1-3-5-10)11-6-8-12(9-7-11)15(17)18/h1-9,16H/b14-13-

38032-13-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (Nz)-N-[(4-nitrophenyl)-phenylmethylidene]hydroxylamine

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:38032-13-2 SDS

38032-13-2Relevant academic research and scientific papers

Synthesis, herbicidal evaluation, and structure-activity relationship of benzophenone oxime ether derivatives

Ma, Jimei,Ma, Mingwei,Sun, Linhao,Zeng, Zhen,Jiang, Hong

, (2015/10/05)

A novel series of benzophenone oxime ether derivatives with tertiary amine groups were synthesized and their herbicidal activities of 24 compounds against Oryza sativa, Sorghum sudanense, Brassica chinensis, and Amaranthus mangostanus L. were also evaluated. Most of these compounds exhibited significant inhibitory effect on root growth at 20 ppm. Based on the herbicidal activity data, computational Three-Dimensional Quantitative Structure-Activity Relationship (3D-QSAR) analysis and molecular docking were undertaken. CoMFA contour maps were generated for the design of benzophenone oxime ether analogues with enhancing activity.

Facile Detosylation of Cyclic Peptides. An Effective Synthesis of Platelet Glycoprotein IIb/IIIa Inhibitors

Zhang, Lin-hua,Ma, Philip

, p. 5765 - 5768 (2007/10/02)

A general effective synthesis of cyclic pentapeptides containing Arg-Gly-Asp sequence, which are potent antithrombotic agents, is reported.

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