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3-(naphthalen-2-yl)pentan-3-ol is an organic compound with a molecular formula of C15H18O. It is a derivative of pentanol, where one of the hydrogen atoms on the pentane chain is replaced by a naphthalene group. This results in a unique structure that combines the properties of both pentanol and naphthalene. The compound is characterized by its aromatic nature due to the presence of the naphthalene ring and its alcohol functionality, which can participate in various chemical reactions such as esterification, oxidation, and substitution. It is typically used in the synthesis of more complex organic molecules and has potential applications in the pharmaceutical and chemical industries.

6241-72-1

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6241-72-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6241-72-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,4 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6241-72:
(6*6)+(5*2)+(4*4)+(3*1)+(2*7)+(1*2)=81
81 % 10 = 1
So 6241-72-1 is a valid CAS Registry Number.

6241-72-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Naphthalenecarbonylazide,3-hydroxy

1.2 Other means of identification

Product number -
Other names 3-hydroxy-2-naphthoyl azide

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:6241-72-1 SDS

6241-72-1Downstream Products

6241-72-1Relevant academic research and scientific papers

A Short Access to Symmetrically α,α-Disubstituted α-Amino Acids from Acyl Cyanohydrins

Boukattaya, Fatma,Caillé, Julien,Ammar, Houcine,Rouzier, Florian,Boeda, Fabien,Pearson-Long, Morwenna S. M.,Bertus, Philippe

, p. 906 - 916 (2016/03/12)

A straightforward synthesis of symmetrically α,α-disubstituted α-amino acids is presented. The key step of this process relies on the efficient double addition of Grignard reagents to acyl cyanohydrins to provide N-acyl amino alcohols selectively in good yields. The chemoselectivity of the reaction was modulated by the nature of the acyl moiety. Eleven amino acids were prepared, including the particularly simple divinylglycine, which is not easily accessible by using conventional methods.

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