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Cyclohexanecarboxylic acid, 3,5-dimethyl-, also known as 3,5-dimethylcyclohexanecarboxylic acid, is an organic compound with the chemical formula C9H16O2. It is a white crystalline solid that is derived from cyclohexane, a cyclic hydrocarbon, by substituting two hydrogen atoms with methyl groups at the 3rd and 5th carbon positions and introducing a carboxylic acid group. Cyclohexanecarboxylic acid, 3,5-dimethyl- is used in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique structure and reactivity. It is typically produced through chemical synthesis methods and is an important building block in the creation of more complex molecules.

7124-21-2

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7124-21-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7124-21-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,2 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7124-21:
(6*7)+(5*1)+(4*2)+(3*4)+(2*2)+(1*1)=72
72 % 10 = 2
So 7124-21-2 is a valid CAS Registry Number.

7124-21-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-dimethylcyclohexane-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names Opt.-inakt. 3.5-Dimethyl-cyclohexancarbonsaeure

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:7124-21-2 SDS

7124-21-2Downstream Products

7124-21-2Relevant academic research and scientific papers

Enantio- and Regioselective Ir-Catalyzed Hydrogenation of Di- and Trisubstituted Cycloalkenes

Peters, Byron K.,Liu, Jianguo,Margarita, Cristiana,Rabten, Wangchuk,Kerdphon, Sutthichat,Orebom, Alexander,Morsch, Thomas,Andersson, Pher G.

supporting information, p. 11930 - 11935 (2016/10/07)

A number of cyclic olefins were prepared and evaluated for the asymmetric hydrogenation reaction using novel N,P-ligated iridium imidazole-based catalysts (Crabtree type). The diversity of these cyclic olefins spanned those having little functionality to

Cycloalkylamides and their therapeutic applications

-

, (2008/06/13)

The present invention relates to the use of compounds of formula (I) for the treatment of a variety of disorders including, but not limited to, epilepsy, bipolar disorder, psychiatric disorders, migraine, pain, neuroprotection, and movement disorders.

Cycloalkylamides and their therapeutic applications

-

, (2008/06/13)

The present invention relates to the use of compounds of formula (I) for the treatment of a variety of disorders including, but not limited to, epilepsy, bipolar disorder, psychiatric disorders, migraine, pain, neuroprotection, and movement disorders.

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