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1988-19-8

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1988-19-8 Usage

General Description

1-Naphthalenol formate (9CI) is a chemical compound with the molecular formula C12H10O2. It is also known as 1-naphthol formate. 1-Naphthalenol,formate(9CI) is a colorless to light yellow liquid with a floral odor. It is primarily used as a fragrance ingredient in perfumes and personal care products. 1-Naphthalenol formate can also be used as a flavoring agent in food and beverages. It is important to handle this chemical with caution, as it can cause irritation to the skin, eyes, and respiratory system. Additionally, it may be harmful if ingested or inhaled in large quantities. Overall, this compound is primarily utilized in the fragrance and flavor industries and is subject to safety regulations and handling guidelines.

Check Digit Verification of cas no

The CAS Registry Mumber 1988-19-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,8 and 8 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1988-19:
(6*1)+(5*9)+(4*8)+(3*8)+(2*1)+(1*9)=118
118 % 10 = 8
So 1988-19-8 is a valid CAS Registry Number.

1988-19-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-naphthyl formate

1.2 Other means of identification

Product number -
Other names 1-Naphthyl formate

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:1988-19-8 SDS

1988-19-8Relevant articles and documents

Synthesis of new chiral schiff bases containing bromo- and iodo-functionalized hydroxynaphthalene frameworks

Wang, Ying,Wang, Mei,Wang, Yu,Chen, Yuee,Sun, Licheng

, p. 1381 - 1393 (2011)

Two series of chiral Schiff bases 3a-g and 4a-g containing bromo- and iodo-functionalized hydroxynaphthalene frameworks were conveniently prepared in acceptable to moderate yields by controlled halogenation of hydroxynaphthaldehyde and then condensation of the corresponding mono-, di-, and trihalohydroxynaphthaldehyde with the chiral amino alcohol. Except for 4d, the Schiff bases 3a-g, 4a-c, and 4e-g prepared in the present work have not been reported in literature so far, and they might be used as effective chiral inducers in some asymmetrically synthetic reactions.

Palladium-Catalyzed Carbonylative Synthesis of Aryl Formates under Mild Conditions

Jiang, Li-Bing,Li, Rui,Li, Hao-Peng,Qi, Xinxin,Wu, Xiao-Feng

, p. 1788 - 1791 (2016/06/01)

Aryl formates have been extensively applied as CO sources in CO-free carbonylation reactions. However, there are no catalytic synthetic procedures for their preparation. In this manuscript, we developed a convenient palladium-catalyzed procedure for the synthesis of aryl formates. Good yields were achieved under mild reaction conditions with formic acid as the formyl source. A formyl meeting: A convenient palladium-catalyzed carbonylation procedure for the synthesis of aryl formates is developed. Good yields are achieved under mild reaction conditions with formic acid as the formyl source.

The Baeyer-Villiger Oxidation of Aromatic Aldehydes and Ketones with Hydrogen Peroxide Catalyzed by Selenium Compounds

Syper, Ludwik

, p. 167 - 172 (2007/10/02)

A series of organoselenium compounds was investigated as activators of hydrogen peroxide in the Baeyer-Villiger oxidation.As a result, a convenient and cheap method for transformation of aromatic aldehydes, having polycondensed ring systems or electron-donating substituents, and polymethoxy derivatives of acetophenone, into phenols was elaborated.This method utilizes hydrogen peroxide activated by areneseleninic acids, as oxidizing agent.

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