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5339-01-5

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5339-01-5 Usage

General Description

3-DIMETHYLAMINOPHENYLMETHYLCARBINOL is a chemical compound with the molecular formula C11H17NO. It is a tertiary amine with a hydroxyl group attached to a benzene ring that contains two methyl and one dimethylamine substituents. 3-DIMETHYLAMINOPHENYLMETHYLCARBINOL is commonly used as a chiral auxiliary in organic synthesis and as a reagent for the preparation of chiral alcohols. Additionally, 3-DIMETHYLAMINOPHENYLMETHYLCARBINOL has been found to exhibit anti-inflammatory and anti-nociceptive effects, making it of interest for potential pharmaceutical applications. Overall, this compound is valued for its role in asymmetric synthesis and its potential therapeutic properties.

Check Digit Verification of cas no

The CAS Registry Mumber 5339-01-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,3 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5339-01:
(6*5)+(5*3)+(4*3)+(3*9)+(2*0)+(1*1)=85
85 % 10 = 5
So 5339-01-5 is a valid CAS Registry Number.

5339-01-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[3-(dimethylamino)phenyl]ethanol

1.2 Other means of identification

Product number -
Other names 3-Dimethylamino-α-methylbenzyl Alcohol

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:5339-01-5 SDS

5339-01-5Relevant articles and documents

Photochemical Reaction of N,N-Dimethylanilines with N-Substituted Maleimides Utilizing Benzaldehyde as the Photoinitiator

Nikitas, Nikolaos F.,Theodoropoulou, Maria A.,Kokotos, Christoforos G.

supporting information, p. 1168 - 1173 (2021/02/01)

Photoorganocatalysis constitutes a powerful domain of photochemistry and organic synthesis. The scaffold of pyrrolo[3,4-c]quinolinoles exhibits interesting and potent inhibition against various enzymes, making them really promising pharmaceutical targets. Herein, we describe a photochemical methodology for the reaction of N,N-dimethylanilines with N-substituted maleimides, utilizing benzaldehyde as the photoinitiator. A variety of substituted N,N-dimethylanilines and N-substituted maleimides were converted into the corresponding adducts in moderate to high yields.

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