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1,2-Cyclohexanedione, 4-methyl-, dioxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18310-19-5

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18310-19-5 Usage

Type of Compound

Dioxime derivative of 1,2-Cyclohexanedione, 4-methyl-

Usage

Analytical chemistry and organic synthesis

Function

Chelating agent for metal ions

Metal Extraction

Used for extraction and separation of metals in analytical chemistry

Complex Formation

Forms stable complexes with various metal ions

Industrial Applications

Metal extraction and purification processes

Organic Synthesis

Potential applications as a reagent for the preparation of various organic compounds

Safety Precautions

Toxicity; should be handled with care

Ventilation

Requires a well-ventilated area during use

Protective Equipment

Proper personal protective equipment should be worn during handling

Check Digit Verification of cas no

The CAS Registry Mumber 18310-19-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,1 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 18310-19:
(7*1)+(6*8)+(5*3)+(4*1)+(3*0)+(2*1)+(1*9)=85
85 % 10 = 5
So 18310-19-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H12N2O2/c1-5-2-3-6(8-10)7(4-5)9-11/h5,9,11H,2-4H2,1H3

18310-19-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(5-methyl-2-nitrosocyclohexen-1-yl)hydroxylamine

1.2 Other means of identification

Product number -
Other names 4-methyl-cyclohexane-1,2-dione dioxime

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:18310-19-5 SDS

18310-19-5Relevant academic research and scientific papers

Synthesis, crystal structure and cytotoxicity of new oxaliplatin analogues indicating that improvement of anticancer activity is still possible

Galanski, Markus,Yasemi, Afshin,Slaby, Susanna,Jakupec, Michael A.,Arion, Vladimir B.,Rausch, Monika,Nazarov, Alexey A.,Keppler, Bernhard K.

, p. 707 - 714 (2004)

Oxaliplatin, (trans-R,R-cyclohexane-1,2-diamine)oxalatoplatinum(II), has recently been approved for combination chemotherapy of metastatic colorectal cancer. Oxaliplatin is significantly more active than its trans-S,S isomer and the mixture of both enanti

Methyl-substituted trans-1,2-cyclohexanediamines as new ligands for oxaliplatin-type complexes

Habala, Ladislav,Dworak, Claudia,Nazarov, Alexey A.,Hartinger, Christian G.,Abramkin, Sergey A.,Arion, Vladimir B.,Lindner, Wolfgang,Galanski, Markus,Keppler, Bernhard K.

, p. 137 - 146 (2008/09/17)

Three different pathways for the synthesis of substituted trans-(±)-1,2-cyclohexanediamines as new ligands for oxaliplatin-type compounds are presented. The different synthetic routes lead (i) by the synthesis of the compound via ortho-bromination of a su

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