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1-(o-tolyl)cyclobutane-1-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29786-39-8

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29786-39-8 Usage

Nitrile derivative

cyclobutane

Explanation

A nitrile derivative is a compound that contains a nitrile functional group (C≡N). In this case, the parent compound is cyclobutane, a four-membered ring hydrocarbon.

Explanation

The "1-(o-tolyl)" in the name indicates that a methyl group is attached to the ortho position (adjacent to the functional group) of a tolyl (methylphenyl) group.

Explanation

The presence of a nitrile functional group in the compound, which is a carbon-nitrogen triple bond, contributes to its unique reactivity and properties.

Explanation

1-(o-tolyl)cyclobutane-1-carbonitrile is commonly used as an intermediate in the synthesis of various compounds, including those in the pharmaceutical, agrochemical, and organic synthesis industries.

Ortho substitution

o-tolyl

Nitrile functional group

C≡N

Applications

pharmaceuticals, agrochemicals, and organic synthesis

Check Digit Verification of cas no

The CAS Registry Mumber 29786-39-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,7,8 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 29786-39:
(7*2)+(6*9)+(5*7)+(4*8)+(3*6)+(2*3)+(1*9)=168
168 % 10 = 8
So 29786-39-8 is a valid CAS Registry Number.

29786-39-8Relevant academic research and scientific papers

Oxadiazole Amine Derivative Compounds as Histone Deacetylase 6 Inhibitor, and the Pharmaceutical Composition Comprising the same

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Paragraph 0600-0603, (2017/07/18)

The present invention relates to a novel compound having an activity of inhibiting histone deacetylase 6 (HDAC6), an optical isomer thereof or a pharmaceutically acceptable salt thereof, a use thereof for preparation of a drug for treatment, a pharmaceutical composition comprising the same, a treatment method using the composition, and a method for preparing the same. The novel compound, an optical isomer thereof or a pharmaceutically acceptable salt thereof according to the present invention has an activity of inhibiting histone deacetylase 6 (HDAC6), and is effective for preventing or treating HDAC6-related diseases, including infectious diseases; neoplasm; endocrine, nutritional and metabolic diseases; mental and behavior disorders; nerve disorders; eye and adnexa diseases; cardiovascular diseases; respiratory diseases; digestive organ diseases; skin and subcutaneous tissue diseases; musculoskeletal and connective tissue diseases; or congenital malformation, deformation and chromosomal abnormality.COPYRIGHT KIPO 2017

NOVEL TRPV3 MODULATORS

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Paragraph 0253; 0272, (2013/06/27)

Disclosed herein are modulators of TRPV3 of formula (I) wherein G1, X1, X2, X3, X4, X5, G2, Z1, Ra, Rb, u, and p are as defined in the specification. Compositions comprising such compounds and methods for treating conditions and disorders using such compounds and compositions are also presented.

NOVEL TRPV3 MODULATORS

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Page/Page column 43, (2012/03/09)

Disclosed herein are modulators of TRPV3 of formula (I), wherein G1, X1, X2, X3, X4, X5, G2, Z1, Ra, Rb, u, and p are as defined in the specifica

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