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4,5,8-Trimethyl-3,4-dihydronaphthalene-1(2H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10468-61-8

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10468-61-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10468-61-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,6 and 8 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 10468-61:
(7*1)+(6*0)+(5*4)+(4*6)+(3*8)+(2*6)+(1*1)=88
88 % 10 = 8
So 10468-61-8 is a valid CAS Registry Number.

10468-61-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5,8-trimethyl-3,4-dihydro-2H-naphthalen-1-one

1.2 Other means of identification

Product number -
Other names 1(2H)-Naphthalenone, 3,4-dihydro-4,5,8-trimethyl-

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:10468-61-8 SDS

10468-61-8Downstream Products

10468-61-8Relevant academic research and scientific papers

Synthesis of 1-tetralones by intramolecular Friedel-Crafts reaction of 4-arylbutyric acids using Lewis acid catalysts

Cui, Dong-Mei,Kawamura, Masato,Shimada, Shigeru,Hayashi, Teruyuki,Tanaka, Masato

, p. 4007 - 4010 (2003)

Intramolecular Friedel-Crafts reaction of 4-arylbutyric acids efficiently proceeded in the presence of catalytic amounts of Lewis acids such as Bi(NTf2)3 and M(OTf)3 (M=Bi, Ga, In and rare-earth metals) to form 1-tetralones. Chroman-4-one and thiochroman-4-one were also obtained in good yields from 3-phenoxypropionic acid and 3-phenylthiopropionic acid, respectively.

Design, synthesis, structure, and dehydrogenation reactivity of a water soluble o-iodoxybenzoic acid derivative bearing a trimethylammonium group

Cui, Li-Qian,Dong, Zhi-Lei,Liu, Kai,Zhang, Chi

supporting information; experimental part, p. 6488 - 6491 (2012/02/02)

5-Trimethylammonio-1, 3-dioxo-1, 3-dihydro-1λ5-benzo[d][1, 2]iodoxol-1-ol anion (AIBX 1a), an o-iodoxybenzoic acid (IBX) derivative having the trimethylammonium moiety on its phenyl ring, possesses very good solubility in water and distinct oxidative properties from IBX, which is demonstrated in the oxidation of various β-keto esters to the corresponding dehydrogenated products using water as cosolvent. The regeneration of AIBX 1a can be easily realized from the reaction mixture due to its good water solubility.2011 American Chemical Society.

SCHWEFELVERBINDUNGEN DES ERDOELS XV. METHYL-5,6,7,8-TETRAHYDRODINAPHTHOTHIOPHENE UND METHYLDINAPHTHOTHIOPHENE

Boberg, Friedrich,Jachiewicz, Adam,Garming, Alfons

, p. 1 - 12 (2007/10/02)

A one pot synthesis gives methyl-5,6,7,8-tetrahydrodinaphthothiophenes (7) from methyl-1,2,3,4-tetrahydronaphthalen-1-ones (1) by bromination and sulfurization.Tetrahydro compounds 7 have been dehydrogenated to corresponding dinaphthothiophenes 8.Proofs for the constitutions are nmr data of 7, 8 and the independent synthesis of one compound 8.A reaction mechanism with 1,4-dithiine intermediates is discussed. Key words: Alkyl-1,2,3,4-tetrahydronaphthalen-1-ones; alkyl-5,6,7,8-tetrahydrodinaphthothiophenes; alkyldinaphthothiophenes; dehydrogenation with o-chlorobenzoquinone.

Organic Reactions Catalyzed by Solid Superacids. 5. Perfluorinated Sulfonic Acid Resin (Nafion-H) Catalyzed Intramolecular Friedel-Crafts Acylation

Yamato, Takehiko,Hideshima, Chieko,Prakash, G. K. Surya,Olah, George A.

, p. 3955 - 3957 (2007/10/02)

Nafion-H, a perfluorinated sulfonic acid resin, catalyzed the intramolecular Friedel-Crafts acylation of diarylalkane-2-carboxylic acids and arylalkanoic acids in refluxing p-xylene to provide cyclic ketones.The reactions were clean, and the water that was formed as a byproduct did not deactivate the catalyst.It was also found that the intramolecular acylation of the corresponding acid chlorides occurred under much milder reaction conditions.The mechanism of the reaction is discussed.

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