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2-Naphthalenemethanol, α-butyl-, also known as 2-(1-butyl)-2-naphthol or 2-naphthol, 2-(1-butyl)-, is an organic compound with the chemical formula C15H16O. It is a colorless to pale yellow liquid with a molecular weight of 212.29 g/mol. 2-Naphthalenemethanol, a-butyl- is characterized by the presence of a naphthalene ring with a hydroxyl group at the 2-position and a butyl group attached to the same carbon. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its potential applications and chemical properties, 2-naphthol derivatives, including α-butyl-2-naphthol, are of interest in the chemical industry for further research and development.

3099-65-8

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3099-65-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3099-65-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,9 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3099-65:
(6*3)+(5*0)+(4*9)+(3*9)+(2*6)+(1*5)=98
98 % 10 = 8
So 3099-65-8 is a valid CAS Registry Number.

3099-65-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(naphthalen-2-yl)pentan-1-ol

1.2 Other means of identification

Product number -
Other names 1-(2-Naphthyl)-pentanol-(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:3099-65-8 SDS

3099-65-8Downstream Products

3099-65-8Relevant academic research and scientific papers

Formation of Secondary Alcohols from the Reaction of Trimethyl- and Methyldiphenyl-telluronium Salts with Aldehydes by Use of Organolithium Reagents

Shi, Li-Lan,Zhou, Zhang-Lin,Huang, Yao-Zeng

, p. 2847 - 2848 (2007/10/02)

The telluronium salts (1) and (2), precursors of the non-stabilized telluronium ylide, on treatment with organolithium reagents, reacted with aldehydes to afford secondary alcohols via tetraorganyl tellurium intermediates.

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