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Cyclohexanone, 2-iodo-3-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

116016-05-8

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116016-05-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116016-05-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,0,1 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 116016-05:
(8*1)+(7*1)+(6*6)+(5*0)+(4*1)+(3*6)+(2*0)+(1*5)=78
78 % 10 = 8
So 116016-05-8 is a valid CAS Registry Number.

116016-05-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-iodo-3-methylcyclohexan-1-one

1.2 Other means of identification

Product number -
Other names 2-iodo-3-methylcyclohexanone

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:116016-05-8 SDS

116016-05-8Relevant academic research and scientific papers

Synthesis of β-substituted α-iodo cycloalkanones by the CuI-mediated conjugate addition of Grignard reagents to α-iodo cycloalkenones

Sha, Chin-Kang,Tseng, Chen-Tso,Chang, Wen-Sheng

, p. 683 - 685 (2007/10/03)

CuI-mediated conjugate addition of Grignard reagents to α-iodo cycloalkenones afforded β-substituted α-iodo cycloalkanones in good to excellent yields.

A New α-Iodination of Ketones Using Iodine-Cerium(IV) Ammonium Nitrate

Horiuchi, C. Akira,Kiji, Shinji

, p. 31 - 34 (2007/10/02)

Direct α-iodination of some ketones using iodine-cerium(IV) ammonium nitrate in acetic acid or methanol, gave the corresponding α-iodoketone in high yield.In the case of 2-pentanone, 4-methyl-2-pentanone, 2-hexanone, and 2-heptanone in methanol, the regioselective products were obtained.

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