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13398-65-7

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13398-65-7 Usage

General Description

2-(2,4-Dimethoxyphenyl)ethanol is an organic compound with the chemical formula C11H16O3. It is a phenolic ether that contains two methoxy groups and an ethyl chain. 2-(2,4-DIMETHOXYPHENYL)ETHANOL is commonly used as a fragrance and flavoring agent due to its pleasant and sweet aroma. It is also used in the production of perfumes, soaps, and other personal care products. Additionally, 2-(2,4-Dimethoxyphenyl)ethanol has been studied for its potential medicinal uses, including its antioxidant and anti-inflammatory properties. However, it is important to use caution when handling this chemical, as it can cause irritation to the skin and eyes.

Check Digit Verification of cas no

The CAS Registry Mumber 13398-65-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,9 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13398-65:
(7*1)+(6*3)+(5*3)+(4*9)+(3*8)+(2*6)+(1*5)=117
117 % 10 = 7
So 13398-65-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O3/c1-12-9-4-3-8(5-6-11)10(7-9)13-2/h3-4,7,11H,5-6H2,1-2H3

13398-65-7SDS

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 2-(2,4-dimethoxyphenyl)ethanol

1.2 Other means of identification

Product number -
Other names 2-(2,4-Dimethoxy-phenyl)-aethanol-(1)

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:13398-65-7 SDS

13398-65-7Relevant articles and documents

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Winstein et al.

, p. 328,330,332 (1956)

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New synthetic route to (S)-(-)-equol through allylic substitution

Takashima, Yuji,Kobayashi, Yuichi

, p. 5156 - 5158 (2008/12/20)

Allylic substitution of allylic picolinate 5 with a copper reagent derived from p-MeOC6H4MgBr (6) and CuBr·Me2S produced the anti SN2′ product 7 with high regioselectivity and efficient chirality transfer. Oxidative cleavage of the olefinic function to the alcohol followed by bromination afforded bromide 16, which upon demethylation and intramolecular ether ring formation furnished (S)-(-)-equol (3).

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