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4-BROMO-ALPHA,ALPHA,ALPHA-TRIFLUORO-O-TO LUIDINE HYDROCHLORIDE, 98 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80997-89-3

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80997-89-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80997-89-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,9,9 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 80997-89:
(7*8)+(6*0)+(5*9)+(4*9)+(3*7)+(2*8)+(1*9)=183
183 % 10 = 3
So 80997-89-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H5BrF3N.ClH/c8-4-1-2-6(12)5(3-4)7(9,10)11;/h1-3H,12H2;1H

80997-89-3SDS

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-α,α,α-TRIFLUORO-O-TO LUIDINE HYDROCHLORIDE, 98

1.2 Other means of identification

Product number -
Other names 4,4Ethylenedipiperidine2HCl

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:80997-89-3 SDS

80997-89-3Downstream Products

80997-89-3Relevant academic research and scientific papers

Alternative method for the reduction of aromatic nitro to amine using TMDS-iron catalyst system

Pehlivan, Leyla,Métay, Estelle,Laval, Stéphane,Dayoub, Wissam,Demonchaux, Patrice,Mignani, Gérard,Lemaire, Marc

experimental part, p. 1971 - 1976 (2011/04/22)

The system 1,1,3,3-tetramethyldisiloxane (TMDS)/Fe(acac)3 is reported here as a new method to obtain amines from aromatic nitro compounds. Amines are synthetized in a straightforward step and are isolated as hydrochloride salts with good to excellent yields. This system has shown a good selectivity toward aryl-chloride, aryl-bromide, ester, carboxylic acid, and cyano groups. The reduction of alkylnitro compounds was unfortunately not possible using this method, only a mixture of mono and dialkylated amine was obtained.

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