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87679-18-3

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87679-18-3 Usage

General Description

(1s,3R,5S)-3,5-dimethylcyclohexane-1-carboxylic acid is a chemical compound with the molecular formula C9H16O2. It is an organic carboxylic acid with a cyclohexane ring and two methyl groups attached to it. The stereochemistry of the compound is specified by the (1s,3R,5S) designation, indicating the configuration of the chiral centers in the molecule. (1s,3R,5S)-3,5-dimethylcyclohexane-1-carboxylic acid can be used in various organic synthesis reactions and is also a potential building block for the synthesis of pharmaceuticals and other biologically active compounds. Its properties and reactivity make it a valuable compound in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 87679-18-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,6,7 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 87679-18:
(7*8)+(6*7)+(5*6)+(4*7)+(3*9)+(2*1)+(1*8)=193
193 % 10 = 3
So 87679-18-3 is a valid CAS Registry Number.

87679-18-3Relevant articles and documents

AMINO-ACID ANILIDES AS SMALL MOLECULE MODULATORS OF IL-17

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Page/Page column 110, (2020/07/14)

The present invention relates to a compound according to formula I (I) and pharmaceutically acceptable salts, hydrates, or solvates thereof. The invention further relates to said compounds for use in therapy, to pharmaceutical compositions comprising said compounds, to methods of treating diseases, e.g. dermal diseases, with said compounds, and to the use of said compounds in the manufacture of medicaments.

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

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