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34328-47-7

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34328-47-7 Usage

General Description

4-Bromo-3-trifluoromethyl-benzaldehyde is a chemical compound with the molecular formula C8H5BrF3O. It is a white to light yellow solid with a strong odor. It is mainly used as an intermediate for the synthesis of various pharmaceuticals, agrochemicals, and organic compounds. 4-BROMO-3-TRIFLUOROMETHYL-BENZALDEHYDE is also used in the production of flavoring agents, as well as in the manufacturing of dyes and pigments. It is important to handle this compound with care, as it can be harmful if ingested, inhaled, or in contact with the skin or eyes.

Check Digit Verification of cas no

The CAS Registry Mumber 34328-47-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,3,2 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 34328-47:
(7*3)+(6*4)+(5*3)+(4*2)+(3*8)+(2*4)+(1*7)=107
107 % 10 = 7
So 34328-47-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H4BrF3O/c9-7-2-1-5(4-13)3-6(7)8(10,11)12/h1-4H

34328-47-7SDS

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 4-bromo-3-(trifluoromethyl)benzaldehyde

1.2 Other means of identification

Product number -
Other names 4-BROMO-3-TRIFLUOROMETHYL-BENZALDEHYDE

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:34328-47-7 SDS

34328-47-7Relevant articles and documents

Molecules having pesticidal utility, and intermediates, compositions, and processes, related thereto

-

, (2018/10/21)

This disclosure relates to the field of molecules having pesticidal utility against pests in Phyla Arthropoda, Mollusca, and Nematoda, processes to produce such molecules, intermediates used in such processes, pesticidal compositions containing such molecules, and processes of using such pesticidal compositions against such pests. These pesticidal compositions may be used, for example, as acaricides, insecticides, miticides, molluscicides, and nematicides. This document discloses molecules having the following formula (“Formula One”).

Halogen-lithium exchange between substituted dihalobenzenes and butyllithium: Application to the regioselective synthesis of functionalized bromobenzaldehydes

Da?browski, Marek,Kubicka, Joanna,Luliński, Sergiusz,Serwatowski, Janusz

, p. 6590 - 6595 (2007/10/03)

Halogen-lithium interconversion reactions between unsymmetrically substituted mono- and bifunctional dihalobenzenes C6H 3XHal2 and C6H2XYHal2 (Hal=Br, I; X, Y=F, OR, CF3, CH(OMe)2) and butyllithium were investigated. The resultant organolithium intermediates were converted into the corresponding benzaldehydes in moderate to good yields. As a rule, bromine atoms in the position ortho to the functional group were replaced preferentially with lithium. Intramolecular competition experiments with bifunctional systems revealed that fluorine is capable of activating the neighboring bromine atom more strongly than methoxy and dimethoxymethyl groups. On the replacement of the non-activated bromine with iodine a complete reversal of this reactivity pattern can be accomplished due to the preferred iodine-lithium exchange.

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