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118664-99-6

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118664-99-6 Usage

General Description

Benzene, 1-chloro-2-fluoro-4-methyl-5-nitro- is a chemical compound with the molecular formula C7H5ClFNO2. It is a nitro derivative of chlorofluoromethylbenzene, containing a chlorine atom, a fluorine atom, a methyl group, and a nitro group attached to a benzene ring. Benzene, 1-chloro-2-fluoro-4-methyl-5-nitro- is used in the synthesis of pharmaceuticals and agrochemical products. It is also used as an intermediate in organic synthesis and as a starting material in the production of specialty chemicals. Due to its potential hazards, including its toxicity and environmental impact, safety precautions should be followed when handling and using this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 118664-99-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,6,6 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 118664-99:
(8*1)+(7*1)+(6*8)+(5*6)+(4*6)+(3*4)+(2*9)+(1*9)=156
156 % 10 = 6
So 118664-99-6 is a valid CAS Registry Number.

118664-99-6SDS

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-Chloro-2-fluoro-4-methyl-5-nitrobenzene

1.2 Other means of identification

Product number -
Other names 1-chloro-2-fluoro-4-methyl-5-nitrobenzene

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:118664-99-6 SDS

118664-99-6Relevant articles and documents

Use of a modified Leimgruber-Batcho reaction to prepare 6-chloro-5-fluoroindole

Bentley, Jon M.,Davidson, James E.,Duncton, Matthew A. J.,Giles, Paul R.,Pratt, Robert M.

, p. 2295 - 2300 (2004)

An efficient synthesis of the title indole, the heterocyclic core of the standard 5-HT2C receptor agonist Ro 60-0175, via a modified Leimgruber-Batcho indole synthesis is presented. The process can be used to make > 100 g quantities of the targ

ANTITUMOR-EFFECT ENHANCER USING PYRAZOLO[3,4-D]PYRIMIDINE COMPOUND

-

Paragraph 0361, (2020/01/22)

To provide a method for treating cancer using a pyrazolo[3,4-d]pyrimidine compound or a salt thereof. The present invention provides an antitumor agent comprising a pyrazolo[3,4-d]pyrimidine compound of formula (I) wherein X, Y, Z1, Z2/su

Indoline derivatives as 5-HT2C receptor agonists

Bentley,Adams,Bebbington,Benwell,Bickerdike,Davidson,Dawson,Dourish,Duncton,Gaur,George,Giles,Hamlyn,Kennett,Knight,Malcolm,Mansell,Misra,Monck,Pratt,Quirk,Roffey,Vickers,Cliffe

, p. 2367 - 2370 (2007/10/03)

A series of 1-(1-indolinyl)-2-propylamines was synthesised and evaluated as 5-HT2C receptor agonists for the treatment of obesity. The general methods of synthesis of the precursor indoles are described. The functional efficacy and radioligand

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