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123871-61-4

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123871-61-4 Usage

Structure

A cyclohexadienone ring with a fluorine and nitro group attached to it

Usage

In organic synthesis and chemical research as a building block for creating more complex molecules

Reactivity

Diverse chemical reactivity

Potential applications

Pharmaceutical and materials science fields

Handling precautions

Can be toxic and harmful if not used properly

Check Digit Verification of cas no

The CAS Registry Mumber 123871-61-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,8,7 and 1 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 123871-61:
(8*1)+(7*2)+(6*3)+(5*8)+(4*7)+(3*1)+(2*6)+(1*1)=124
124 % 10 = 4
So 123871-61-4 is a valid CAS Registry Number.

123871-61-4SDS

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 6-Fluoro-6-nitro-2,4-cyclohexadien-1-one

1.2 Other means of identification

Product number -
Other names 6-fluoro-6-nitrocyclohexa-2,4-dienone

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:123871-61-4 SDS

123871-61-4Upstream product

123871-61-4Downstream Products

123871-61-4Relevant articles and documents

Formation of 4-Halo-4-nitrocyclohexa-2,5-dienones on Nitration of p-Halophenols and p-Halophenyl Acetates.

Clewley, Robin G.,Cross, Gordon G.,Fischer, Alfred,Henderson, George N.

, p. 1299 - 1310 (2007/10/02)

Nitration of p-chloro-, p-fluoro-, and p-bromo-phenol or the corresponding p-halophenyl acetates at -40 deg C and below gives the 4-halo-4-nitrocyclohexa-2,5-dienones in addition to the 4-halo-2-nitrophenols.The dienones isomerize to the nitrophenols at temperatures between -40 deg C and 0 deg C.Nitration of 4-chloro-2-methylphenol or its acetate gives both 4-chloro-2-methyl-4-nitrocyclohexa-2,5-dienone and 4-chloro-6-methyl-6-nitrocyclohexa-2,4-dienone. 4-Chloro-3-methylphenol and its acetate give 4-chloro-3-methyl-4-nitrocyclohexa-2,5-dienone.

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