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2-Nitro-benzoesaeure-<2-brom-anilid> is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34489-84-4

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34489-84-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34489-84-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,4,8 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 34489-84:
(7*3)+(6*4)+(5*4)+(4*8)+(3*9)+(2*8)+(1*4)=144
144 % 10 = 4
So 34489-84-4 is a valid CAS Registry Number.

34489-84-4SDS

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 2-Nitro-benzoesaeure-[2-brom-anilid]

1.2 Other means of identification

Product number -
Other names 2-Nitro-benzoesaeure-(2-brom-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:34489-84-4 SDS

34489-84-4Relevant academic research and scientific papers

Deep eutectic solvent mediated synthesis of quinazolinones and dihydroquinazolinones: Synthesis of natural products and drugs

Ghosh, Suman Kr,Nagarajan, Rajagopal

, p. 27378 - 27387 (2016/04/04)

A mild and greener protocol was developed to synthesize substituted quinazolinones and dihydroquinazolinones via deep eutectic solvent (DES) mediated cyclization with a series of aliphatic, aromatic, and heteroaromatic aldehydes in good to excellent yields. This greener strategy was further utilised to synthesize various quinazolinone natural products and drugs.

CuI/l-proline-catalyzed intramolecular aryl amination: An efficient route for the synthesis of 1,4-benzodiazepinones

Majumdar,Ganai, Sintu

scheme or table, p. 1881 - 1887 (2011/10/05)

An effective protocol for the synthesis of potentially bioactive benzo[e]chromeno[6,5-b][1,4]diazepine-3,8(7H,13H)-dione and dibenzo[b,e][1,4] diazepin-11(10H)-one derivatives in good to excellent yields has been achieved by CuI/l-Proline catalyzed coupling reaction as the key step. The methodology offers clean reaction conditions and easy isolation of the products in 61-92% yields.

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