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Ethanone, 1,2-diphenyl-, oxime, (1Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57736-10-4

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57736-10-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57736-10-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,7,3 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 57736-10:
(7*5)+(6*7)+(5*7)+(4*3)+(3*6)+(2*1)+(1*0)=144
144 % 10 = 4
So 57736-10-4 is a valid CAS Registry Number.

57736-10-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-1,2-diphenylethanone oxime

1.2 Other means of identification

Product number -
Other names Oxim des Phenyl-benzyl-ketons

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:57736-10-4 SDS

57736-10-4Upstream product

57736-10-4Relevant academic research and scientific papers

Synthesis of highly substituted pyrroles via nucleophilic catalysis

Ngwerume, Simbarashe,Camp, Jason E.

supporting information; experimental part, p. 6271 - 6274 (2010/11/19)

Figure presented. A nucleophilic catalysis method providing a concise synthesis of di-, tri-, and tetrasubstituted pyrroles is described. This regioselective one-pot method relies on nucleophilic catalysis of the intermolecular addition of oximes to activ

Asymmetric induction in the neber rearrangement of simple ketoxime sulfonates under phase-transfer conditions: Experimental evidence for the participation of an anionic pathway

Ooi, Takashi,Takahashi, Makoto,Doda, Kanae,Maruoka, Keiji

, p. 7640 - 7641 (2007/10/03)

Phase-transfer catalysis has been successfully utilized for the Neber rearrangement of simple ketoxime sulfonates. For instance, treatment of (Z)-1a with p-toluenesulfonyl chloride (1.2 equiv), tetrabutylammonium bromide (5 mol %) and MeOH (10 equiv) in t

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