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327-95-7

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327-95-7 Usage

General Description

4-Fluoroisophthalic acid is a chemical compound with the molecular formula C8H5FO4. It is a derivative of isophthalic acid, and it contains a fluorine atom in the para position relative to the carboxylic acid group. 4-Fluoroisophthalic acid is commonly used in organic synthesis as a building block for the preparation of various pharmaceuticals, agrochemicals, and functional materials. It is also utilized in the production of fluorescent dyes, polymers, and coordination complexes. 4-Fluoroisophthalic acid is a white solid with a high melting point and is generally handled and stored as a solid powder. It is important to handle this compound with caution due to its potential irritant and toxic properties.

Check Digit Verification of cas no

The CAS Registry Mumber 327-95-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,2 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 327-95:
(5*3)+(4*2)+(3*7)+(2*9)+(1*5)=67
67 % 10 = 7
So 327-95-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H5FO4/c9-6-2-1-4(7(10)11)3-5(6)8(12)13/h1-3H,(H,10,11)(H,12,13)

327-95-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-fluorobenzene-1,3-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names 4-Fluor-isophthalsaeure

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:327-95-7 SDS

327-95-7Relevant articles and documents

The first regioselective metalation and functionalization of unprotected 4-halobenzoic acids

Gohier, Frederic,Castanet, Anne-Sophie,Mortier, Jacques

, p. 1501 - 1504 (2007/10/03)

(Chemical Equation Presented) By treatment with s-BuLi, s-BuLi/TMEDA, or t-BuLi at ~-78°C, 4-fluoro- and 4-chlorobenzoic acids (1a,b) are metalated preferentially in the position adjacent to the carboxylate. A complete reversal in regioselectivity is observed for 1a when treated with LTMP; a sequential process involving a rapid intraaggregate lithiation through a quasi dianion complex "QUADAC" is postulated to explain the unusual reactivity of Me2S2 and I2.

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