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Benzaldehyde, 4-amino-3-bromo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42580-44-9

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42580-44-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42580-44-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,5,8 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 42580-44:
(7*4)+(6*2)+(5*5)+(4*8)+(3*0)+(2*4)+(1*4)=109
109 % 10 = 9
So 42580-44-9 is a valid CAS Registry Number.

42580-44-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-amino-3-bromobenzaldehyde

1.2 Other means of identification

Product number -
Other names Benzaldehyde,4-amino-3-bromo

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:42580-44-9 SDS

42580-44-9Relevant academic research and scientific papers

Regiospecific oxidation of an alkyl group of aromatic amine to carbonyl group by DDQ in aq. medium

Mane, Madhav S.,Balaskar, Ravi S.,Gavade, Sandip N.,Pabrekar, Pramod N.,Shingare, Murlidhar S.,Mane, Dhananjay V.

experimental part, p. 1039 - 1042 (2012/06/01)

The regiospecific oxidation of alkyl group of both sterically hindered and unhindered aromatic amine to corresponding carbonyl compound was done in aq. medium by using DDQ. The optimized reaction protocol was found to be most simple, high yielding and novel method for oxidation of alkyl group of aromatic amine in to its carbonyl compound.

Substituted phenyl farnesyltransferase inhibitors

-

, (2012/09/25)

Compounds of formula (I) or pharmaceutically acceptable salts thereof, inhibit farnesyltransferase. Methods for making the compounds, pharmaceutical compositions containing the compounds, and methods of treatment using the compounds are disclosed.

Simple Synthetic Route to 4-Aminobenzaldehydes from Anilines

Liedholm, Brita

, p. 2235 - 2242 (2007/10/02)

Anilines unsubstituted at the 4-position react under mild conditions in Me2SO-HCl solvent (H+ = 0.6 mol dm-3) to give substituted 4-aminobenzaldehydes in high yields; although addition of CuCl2 gives a cleaner product, it is not esse

REGIOSPECIFIC OXIDATION BY DDQ OF UNHINDERED ALKYL GROUPS IN STERICALLY HINDERED AROMATIC AMINES

Lal, Bansi,Gidwani, Ramesh M.,Reden, Jurgen,Souza, Noel J. de

, p. 2901 - 2904 (2007/10/02)

DDQ oxidises an unhindered activated alkyl group to a carbonyl or a hydroxymethyl group depending on the nature of the substitution, in a sterically hindered aromatic amine.

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