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1,4-DIHYDRO-3,5-DIMETHYLBENZOIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

31673-46-8

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31673-46-8 Usage

Appearance

White crystalline solid

Natural sources

Veratrum album and Vanilla planifolia plants

Antioxidant

Exhibits antioxidant properties

Cardiovascular disease

Studied for potential therapeutic effects

Diabetes

Studied for potential therapeutic effects

Inflammation

Studied for potential therapeutic effects

Fragrances

Used in the production of fragrances

Flavors

Used in the production of flavors

Pharmaceuticals

Used in the production of pharmaceuticals

Vanillin precursor

Serves as a precursor in the synthesis of vanillin, a popular flavoring agent in the food industry

Check Digit Verification of cas no

The CAS Registry Mumber 31673-46-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,6,7 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 31673-46:
(7*3)+(6*1)+(5*6)+(4*7)+(3*3)+(2*4)+(1*6)=108
108 % 10 = 8
So 31673-46-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H12O2/c1-6-3-7(2)5-8(4-6)9(10)11/h4-5,8H,3H2,1-2H3,(H,10,11)

31673-46-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-dimethylcyclohexa-2,5-diene-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1,4-DIHYDRO-3,5-DIMETHYLBENZOIC ACID

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:31673-46-8 SDS

31673-46-8Relevant academic research and scientific papers

Non-Cryogenic, Ammonia-Free Reduction of Aryl Compounds

-

, (2022/03/31)

A method of reducing an aromatic ring or a cyclic, allylic ether in a compound includes preparing a reaction mixture including a compound including an aromatic moiety or a cyclic, allylic ether moiety, an alkali metal, and either ethylenediamine, diethylenetriamine, triethylenetetramine, or a combination thereof, in an ether solvent; and reacting the reaction mixture at from ?20° C. to 30° C. for a time sufficient to reduce a double bond in the aromatic moiety to a single bond or to reduce the cyclic, allylic ether moiety.

Scalable and safe synthetic organic electroreduction inspired by Li-ion battery chemistry

Peters, Byron K.,Rodriguez, Kevin X.,Reisberg, Solomon H.,Beil, Sebastian B.,Kawamata, Yu,Baran, Phil S.,Hickey, David P.,Klunder, Kevin,Gorey, Timothy J.,Anderson, Scott L.,Minteer, Shelley D.,Collins, Michael,Starr, Jeremy,Chen, Longrui,Udyavara, Sagar,Neurock, Matthew

, p. 838 - 845 (2019/04/30)

Reductive electrosynthesis has faced long-standing challenges in applications to complex organic substrates at scale. Here, we show how decades of research in lithium-ion battery materials, electrolytes, and additives can serve as an inspiration for achieving practically scalable reductive electrosynthetic conditions for the Birch reduction. Specifically, we demonstrate that using a sacrificial anode material (magnesium or aluminum), combined with a cheap, nontoxic, and water-soluble proton source (dimethylurea), and an overcharge protectant inspired by battery technology [tris(pyrrolidino)phosphoramide] can allow for multigram-scale synthesis of pharmaceutically relevant building blocks. We show how these conditions have a very high level of functional-group tolerance relative to classical electrochemical and chemical dissolving-metal reductions. Finally, we demonstrate that the same electrochemical conditions can be applied to other dissolving metal-type reductive transformations, including McMurry couplings, reductive ketone deoxygenations, and epoxide openings.

Regioselective Transfer Hydrodeuteration of Alkenes with a Hydrogen Deuteride Surrogate Using B(C6F5)3 Catalysis

Walker, Johannes C. L.,Oestreich, Martin

supporting information, p. 6411 - 6414 (2018/10/20)

A regioselective hydrodeuteration of alkenes using monodeuterated cyclohexa-1,4-dienes as surrogates for hydrogen deuteride (HD) gas is reported. The metal-free process proceeds under B(C6F5)3 catalysis presumably by deuteride abstraction to form borodeuteride [DB(C6F5)3]a and highly Br?nsted-acidic Wheland intermediates. Low catalyst loadings (2.5 mol %) are used, and the reaction proceeds at room temperature.

Nucleophile-Assisted Alkene Activation: Olefins Alone Are Often Incompetent

Ashtekar, Kumar Dilip,Vetticatt, Mathew,Yousefi, Roozbeh,Jackson, James E.,Borhan, Babak

supporting information, p. 8114 - 8119 (2016/07/16)

Emerging work on organocatalytic enantioselective halocyclizations naturally draws on conditions where both new bonds must be formed under delicate control, the reaction regime where the concerted nature of the AdE3 mechanism is of greatest importance. Without assistance, many simple alkene substrates react slowly or not at all with conventional halenium donors under synthetically relevant reaction conditions. As demonstrated earlier by Shilov, Cambie, Williams, Fahey, and others, alkenes can undergo a concerted AdE3-type reaction via nucleophile participation, which sets the configuration of the newly created stereocenters at both ends in one step. Herein, we explore the modulation of alkene reactivity and halocyclization rates by nucleophile proximity and basicity, through detailed analyses of starting material spectroscopy, addition stereopreferences, isotope effects, and nucleophile-alkene interactions, all obtained in a context directly relevant to synthesis reaction conditions. The findings build on the prior work by highlighting the reactivity spectrum of halocyclizations from stepwise to concerted, and suggest strategies for design of new reactions. Alkene reactivity is seen to span the range from the often overgeneralized "sophomore textbook" image of stepwise electrophilic attack on the alkene and subsequent nucleophilic bond formation, to the nucleophile-assisted alkene activation (NAAA) cases where electron donation from the nucleophilic addition partner activates the alkene for electrophilic attack. By highlighting the factors that control reactivity across this range, this study suggests opportunities to explain and control stereo-, regio-, and organocatalytic chemistry in this important class of alkene additions.

C19 quassinoid model studies: Preparation of trans-perhydroindans via a vinylogous Mukaiyama aldol - Free-radical cyclization route

Donahue, Matthew G.,Hart, David J.

, p. 314 - 317 (2007/10/03)

Aldehyde 9 was prepared in 5 steps from 3,5-dimethylbenzoic acid. Treatment of 9 with ketene acetals 10 and 19 and titanium tetrachloride gave free-radical cyclization substrates 11 and 20 in 67% and 51% yields, respectively. Tri-n-butylstannane-mediated

X-Ray Crystallographic Study of the Preferred Conformations of 2,6- and 3,5-Dimethyl-1,4-dihydrobenzoic Acids

Grossel, Martin C.,Cheetham, Anthony K.,James, Daniel,Newsam, John M.

, p. 471 - 475 (2007/10/02)

A single-crystal X-ray diffraction study of 2,6-dimethyl-1,4-dihydrobenzoic acid (2b) reveals that the cyclohexadiene ring is somewhat puckered with an angle of pucker, α = 171.6 deg.Crystals are monoclinic, space group P21/n, with Z = 4, in a

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