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Cyclohexanone, 3-methyl-2-(phenylmethyl)-, also known as 3-methyl-2-benzylcyclohexanone, is an organic compound with the chemical formula C14H16O. It is a colorless to pale yellow liquid with a molecular weight of 200.28 g/mol. Cyclohexanone, 3-methyl-2-(phenylmethyl)- is characterized by a cyclohexanone ring, with a methyl group at the 3-position and a benzyl group (phenylmethyl) attached at the 2-position. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactivity and functional groups, it is an important building block in organic chemistry, particularly in the preparation of complex molecules with potential applications in the chemical and pharmaceutical industries.

4061-12-5

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4061-12-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4061-12-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,6 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4061-12:
(6*4)+(5*0)+(4*6)+(3*1)+(2*1)+(1*2)=55
55 % 10 = 5
So 4061-12-5 is a valid CAS Registry Number.

4061-12-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Benzyl-3-methyl-cyclohexanon

1.2 Other means of identification

Product number -
Other names -

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

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More Details:4061-12-5 SDS

4061-12-5Downstream Products

4061-12-5Relevant academic research and scientific papers

Highly Regioselective Monoalkylation of Ketones via Manganese Enolates. Prepared from Lithium Enolates

Cahiez, Gerard,Chau, Khi,Clery, Patrick

, p. 3069 - 3072 (2007/10/02)

Li-enolates are readily converted to Mn-enolates by treatment with manganese halides.In THF, the reaction is easily and economically performed with manganese chloride at room temperature.Mn-enolates can then be regioselectively monoalkylated in good yields.The formation of di and polyalkylated products is never observed (1percent).

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