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71861-99-9

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71861-99-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71861-99-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,8,6 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 71861-99:
(7*7)+(6*1)+(5*8)+(4*6)+(3*1)+(2*9)+(1*9)=149
149 % 10 = 9
So 71861-99-9 is a valid CAS Registry Number.

71861-99-9SDS

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 formic acid-(2,4-dibromo-anilide)

1.2 Other means of identification

Product number -
Other names Ameisensaeure-(2,4-dibrom-anilid)

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:71861-99-9 SDS

71861-99-9Relevant articles and documents

Regiochemistry of nucleophilic substitution of pentachloropyridine with N and O bidentate nucleophiles

Poorfreidoni, Alireza,Ranjbar-Karimi, Reza,Kia, Reza

, p. 4398 - 4406 (2015/06/16)

Site reactivity of some enol-imines derived from N-aryl formamides with pentachloropyridine under basic conditions in dry CH3CN was investigated. The aromatic nucleophilic substitution of pentachloropyridine with enol-imines occurs at the 4-position of pyridine ring by both oxygen and nitrogen site of enol-imines. Nucleophilic attack by the oxygen of enol-imine gave corresponding oximino compounds as a mixture of E- and Z-isomers. In contrast, nucleophilic attack by the nitrogen of enol-imine gave the unexpected N,N-di-substituted aryl compounds. The structures of all the compounds were confirmed by IR, 1H NMR, 13C NMR and 19F NMR spectroscopy as well as elemental analysis and X-ray crystallography.

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