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3937-49-3

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3937-49-3 Usage

General Description

4α-Methylcyclohexane-1β-methanol is a chemical compound with the molecular formula C8H16O. It is a colorless liquid with a mild, minty odor, and it is used as a fragrance and flavoring agent in various consumer products. This chemical is derived from the bicyclic compound menthol and is commonly found in products such as toothpaste, mouthwash, and chewing gum. It has been studied for its potential therapeutic effects, including analgesic and anti-inflammatory properties. However, excessive exposure to this compound can cause irritation to the skin, eyes, and respiratory system. Additionally, it is important to note that this compound should be handled and used with caution due to its potential health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 3937-49-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,3 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3937-49:
(6*3)+(5*9)+(4*3)+(3*7)+(2*4)+(1*9)=113
113 % 10 = 3
So 3937-49-3 is a valid CAS Registry Number.

3937-49-3Downstream Products

3937-49-3Relevant articles and documents

Rhodium(I)-Catalyzed Hydrogenation of Olefins. The Documentation of Hydroxyl-Directed Stereochemical Control in Cyclic and Acyclic Systems

Evans, David A.,Morrissey, Michael M.

, p. 3866 - 3868 (1984)

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Immunomodulator

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Paragraph 0254-0258, (2021/05/22)

The invention discloses an immunomodulator, and particularly relates to a compound for inhibiting IL-17A and application of the compound serving as the immunomodulator in preparation of drugs. The invention discloses application of a compound shown in a formula I or a stereoisomer thereof in preparation of medicines for inhibiting IL-17A, and provides a new choice for clinically screening and/or preparing medicines for treating diseases related to IL-17A activity.

Hydrogenation of alkenes via cooperative hydrogen atom transfer

Kattamuri, Padmanabha V.,West, Julian G.

supporting information, p. 19316 - 19326 (2020/11/13)

Radical hydrogenation via hydrogen atom transfer (HAT) to alkenes is an increasingly important transformation for the formation of thermodynamic alkane isomers. Current single-catalyst methods require stoichiometric oxidant in addition to hydride (H-) source to function. Here we report a new approach to radical hydrogenation: cooperative hydrogen atom transfer (cHAT), where each hydrogen atom donated to the alkene arrives from a different catalyst. Further, these hydrogen atom (H?) equivalents are generated from complementary hydrogen atom precursors, with each alkane requiring one hydride (H-) and one proton (H+) equivalent and no added oxidants. Preliminary mechanistic study supports this reaction manifold and shows the intersection of metal-catalyzed HAT and thiol radical trapping HAT catalytic cycles to be essential for effective catalysis. Together, this unique catalyst system allows us to reduce a variety of unactivated alkene substrates to their respective alkanes in high yields and diastereoselectivities and introduces a new approach to radical hydrogenation.

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