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1125-86-6

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1125-86-6 Usage

Molecular weight

155.24 g/mol

Chemical structure

Cyclic ketoxime with a cyclohexyl group attached to the carbon atom adjacent to the oxime group

Usage

Intermediate in the synthesis of other organic compounds

Function

Chelating agent for metal ions

Applications

Manufacture of pharmaceuticals, pesticides, and other organic chemicals

Potential uses

Production of rubber accelerators and antioxidants, anti-aging properties

Additional studies

Treatment of metal poisoning

Check Digit Verification of cas no

The CAS Registry Mumber 1125-86-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1125-86:
(6*1)+(5*1)+(4*2)+(3*5)+(2*8)+(1*6)=56
56 % 10 = 6
So 1125-86-6 is a valid CAS Registry Number.

1125-86-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-cyclohexyl-propan-1-one oxime

1.2 Other means of identification

Product number -
Other names 1-Cyclohexyl-propan-1-on-oxim

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:1125-86-6 SDS

1125-86-6Relevant articles and documents

A CONVENIENT SYNTHESIS OF KETOXIMES FROM GRIGNARD REAGENTS AND NITRO COMPOUNDS ACTIVATED BY N,N-DIMETHYLCHLOROMETHYLENIMINIUM CHLORIDE

Fujisawa, Tamotsu,Kurita, Yoshitsugu,Sato, Toshio

, p. 1537 - 1540 (2007/10/02)

Ketoximes were synthesized in high yields with a new carbon-carbon bond formation by regioselective nucleophilic attack of Grignard reagents at the α-position of aci-nitroalkanes activated by N,N-dimethylchloromethyleniminium chloride in the presence of a catalitic amount of copper(I) iodide under mild conditions.

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