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1,3-dimethyl-5-[(2-methylprop-2-en-1-yl)oxy]benzene is an organic compound characterized by a benzene ring with two methyl groups attached at the 1st and 3rd carbon positions, and a 2-methylprop-2-en-1-yloxy group (also known as a tert-butyloxy group) attached at the 5th carbon position. This molecule is a derivative of anisole, with the tert-butyloxy group replacing the methoxy group found in the parent compound. It is a colorless liquid with a molecular formula of C12H18O and a molecular weight of 178.27 g/mol. 1,3-dimethyl-5-[(2-methylprop-2-en-1-yl)oxy]benzene is primarily used as a fragrance ingredient in various consumer products, such as perfumes, cosmetics, and detergents, due to its pleasant, floral scent. It is also known for its low toxicity and is considered safe for use in these applications.

3698-47-3

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3698-47-3 Usage

Molecular weight

178.23 g/mol

Appearance

Clear, colorless to pale yellow liquid

Odor

Strong, sweet, and spicy

Source

Derived from essential oils of plants such as basil, bay leaf, and clove

Uses

a. Flavoring agent in food products
b. Fragrance ingredient in perfumes, soaps, and other personal care products
c. Precursor in the synthesis of various chemicals and pharmaceuticals

Safety concerns

Can cause skin irritation and allergic reactions in some individuals

Regulations

Subject to regulations and restrictions in its use in certain products

Check Digit Verification of cas no

The CAS Registry Mumber 3698-47-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,9 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3698-47:
(6*3)+(5*6)+(4*9)+(3*8)+(2*4)+(1*7)=123
123 % 10 = 3
So 3698-47-3 is a valid CAS Registry Number.

3698-47-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-dimethylphenylmercuric chloride

1.2 Other means of identification

Product number -
Other names 3,5-dimethylphenyl methallyl ether

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:3698-47-3 SDS

3698-47-3Downstream Products

3698-47-3Relevant academic research and scientific papers

Iridium-catalyzed enantioselective intramolecular hydroarylation of allylic aryl ethers devoid of a directing group on the aryl group

Kusaka, Satoshi,Ohmura, Toshimichi,Suginome, Michinori

supporting information, p. 13542 - 13545 (2021/12/23)

Although intramolecular hydroarylation is an attractive transformation of allylic aryl ethers, it has suffered from narrow substrate scope. We herein describe Ir/(S)-DTBM-SEGPHOS-catalyzed intramolecular hydroarylation of allylic aryl ethers. The reaction

Synthesis and structure of [Ru(PPh3)2(bipy)(MeCN)Cl][BPh4] and it's catalytic property towards regioselective and stereoselective allylation of phenols

Sinha, Abhilasha,Khatua, Snehadrinarayan,Bhattacharjee, Manish

supporting information, p. 116 - 120 (2015/02/19)

The compound, [Ru(PPh3)2(bipy)(MeCN)Cl][BPh4] (1) has been synthesized from the precursor complex, [Ru(bipy)(PPh3)2Cl2]. The complex has been structurally characterized. This complex has been found to be an efficient catalyst for the regioselective allylation of phenols.

ONE-POT SYNTHESES OF 2,3-DIHYDRO-2,2-DIMETHYLBENZOFURAN DERIVATIVES

Kim, Kyoung Mahn,Kim, Hyoung Rae,Ryu, Eung K.

, p. 497 - 505 (2007/10/02)

A tandem Claisen rearrangement-cyclization reaction of aryl methallyl ethers afforded the corresponding 2,3-dihydro-2,2-dimethylbenzofuran derivatives at -70 deg C with aluminium chloride.

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