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110931-86-7

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110931-86-7 Usage

General Description

5-Fluoro-1-naphthaldehyde is a chemical compound with the molecular formula C11H7FO. It is a yellow crystalline solid that is commonly used as a fluorescent dye for identifying proteins. It is also an important intermediate in the synthesis of pharmaceuticals and agrochemicals. Its chemical structure consists of a naphthalene ring with a fluorine atom and an aldehyde functional group attached to it. The compound is toxic if ingested or inhaled and can cause irritation to the skin, eyes, and respiratory system. It should be handled and used with proper safety precautions in a well-ventilated area.

Check Digit Verification of cas no

The CAS Registry Mumber 110931-86-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,9,3 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 110931-86:
(8*1)+(7*1)+(6*0)+(5*9)+(4*3)+(3*1)+(2*8)+(1*6)=97
97 % 10 = 7
So 110931-86-7 is a valid CAS Registry Number.

110931-86-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-fluoronaphthalene-1-carbaldehyde

1.2 Other means of identification

Product number -
Other names 5-fluoro-1-naphthalenecarboxaldehyde

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:110931-86-7 SDS

110931-86-7Upstream product

110931-86-7Downstream Products

110931-86-7Relevant articles and documents

Synthesis and Structure-Activity Relationships of Naphthalene-Substituted Derivatives of the Allylamine Antimycotic Terbinafine

Nussbaumer, Peter,Dorfstaetter, Gerhard,Leitner, Ingrid,Mraz, Karin,Vypel, Hermann,Stuetz, Anton

, p. 2810 - 2816 (2007/10/02)

Derivatives of the allylamine antimycotic terbinafine (1) with varied substitution at the naphthalene ring system have been prepared, and their antifungal activity has been evaluated.In general, the potency is strongly dependent on the bulkiness of the su

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