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160911-11-5

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160911-11-5 Usage

General Description

3-Fluoro-5-Methylanisole, also known as 3-fluoro-5-methylanisole, is a chemical compound with the molecular formula C8H9FO. It is a colorless to yellow liquid with a fruity odor. This chemical is used in the production of pharmaceuticals, fragrances, and other fine chemicals. It can also be used as an intermediate in organic synthesis. 3-Fluoro-5-Methylanisole is considered to be a potentially hazardous chemical and should be handled and used with caution.

Check Digit Verification of cas no

The CAS Registry Mumber 160911-11-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,9,1 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 160911-11:
(8*1)+(7*6)+(6*0)+(5*9)+(4*1)+(3*1)+(2*1)+(1*1)=105
105 % 10 = 5
So 160911-11-5 is a valid CAS Registry Number.

160911-11-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-fluoro-3-methoxy-5-methylbenzene

1.2 Other means of identification

Product number -
Other names 3-Fluoro-5-methylanisole

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:160911-11-5 SDS

160911-11-5Relevant articles and documents

Synthesis of fused indazole ring systems and application to nigeglanine hydrobromide

Sather, Aaron C.,Berryman, Orion B.,Rebek, Julius

supporting information; experimental part, p. 1600 - 1603 (2012/06/05)

The single-step synthesis of fused tricyclic pyridazino[1,2-a]indazolium ring systems is described. Structural details revealed by crystallography explain the unexpected reactivity. The method is applied to the gram scale synthesis of nigeglanine hydrobro

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