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N-(2-iodocyclohexyl)acetamide is a chemical compound with the molecular formula C8H14INO. It is a derivative of acetamide, where a cyclohexyl group is substituted at the nitrogen atom, and an iodine atom is attached to the cyclohexyl ring at the 2-position. N-(2-iodocyclohexyl)acetamide is characterized by its unique structure, which combines the properties of an amide with the presence of a halogenated cycloalkane. It is often used in organic synthesis and as an intermediate in the preparation of various pharmaceuticals and agrochemicals. The iodine atom in the compound can participate in various chemical reactions, such as nucleophilic substitution or radical reactions, making it a versatile building block in the synthesis of more complex molecules.

7707-58-6

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7707-58-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7707-58-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,0 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7707-58:
(6*7)+(5*7)+(4*0)+(3*7)+(2*5)+(1*8)=116
116 % 10 = 6
So 7707-58-6 is a valid CAS Registry Number.

7707-58-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-iodocyclohexyl)acetamide

1.2 Other means of identification

Product number -
Other names trans-1-acetamido-2-iodocyclohexane

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:7707-58-6 SDS

7707-58-6Downstream Products

7707-58-6Relevant academic research and scientific papers

A general process for the haloamidation of olefins. Scope and mechanism

Yeung, Ying-Yeung,Gao, Xuri,Corey

, p. 9644 - 9645 (2007/10/03)

A methodology is described for the addition of a bromine atom and an amide nitrogen in a trans sense to an olefinic double bond. The process, which is illustrated by numerous examples, involves the use of an N-bromoamide and a Lewis acid as a source of Br

REACTION OF IODOSOFLUOROSULFATE WITH ALKENES

Zefirov, N. S.,Kasumov, T. M.,Koz'min, A. S.,Sorokin, V. D.,Polishchuk, V. R.

, p. 341 - 352 (2007/10/02)

The electrophilic addition of iodosofluorosulfate to a series of acyclic and mono-, bi-, and polycyclic olefins, dienes, and trienes was investigated for the first time. The high electrophilicity of this reagent favors the formation of the intermediate ca

Nitrosonium Ion Promoted Iodination and 1,2-Iodofunctionalization of Cyclohexene

Radner, Finn

, p. 902 - 907 (2007/10/02)

The promoting influence of NO+BF4- on the addition of I2 or 'I+Nu-' couples to cyclohexene (1) in the presence of O2 is described. 1-Acetoxy-2-iodocyclohexane is obtained in 89percent isolated yield from the reaction of I2, 1 and CH3COOH in CH2Cl2, and the corresponding methoxy- and acetamido-substituted iodocyclohexanes are obtained in 96 and 92percent yield, when methanol and acetonitrile, respectively, are added.Applications of the method to the synthesis of cis-1,2-cyclohexanediol (Woodward reaction) and bis(2-iodocyclohexyl) ether is described.

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