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Benzenemethanimine, N-bromo-α-phenyl-, also known as 2-bromobenzylideneaniline or α-bromobenzylideneaniline, is an organic compound with the chemical formula C13H10BrN. It is a derivative of benzenemethanimine, where a bromine atom is attached to the α-carbon of the phenyl group. Benzenemethanimine, N-bromo-a-phenyl- is a colorless to pale yellow solid and is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It is also known for its reactivity in various chemical reactions, such as coupling reactions, and is a valuable building block in organic synthesis. Due to its reactivity, it is important to handle Benzenemethanimine, N-bromo-a-phenyl- with care, as it may be harmful if inhaled, ingested, or absorbed through the skin.

7699-75-4

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7699-75-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7699-75-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,9 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7699-75:
(6*7)+(5*6)+(4*9)+(3*9)+(2*7)+(1*5)=154
154 % 10 = 4
So 7699-75-4 is a valid CAS Registry Number.

7699-75-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name benzhydrylidene-bromo-amine

1.2 Other means of identification

Product number -
Other names Benzhydryliden-brom-amin

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:7699-75-4 SDS

7699-75-4Downstream Products

7699-75-4Relevant academic research and scientific papers

Oxidative conversion of α,α-disubstituted acetamides to corresponding one-carbon-shorter ketones using hypervalent iodine (λ5) reagents in combination with tetraethylammonium bromide

Bellale, Eknath V.,Bhalerao, Dinesh S.,Akamanchi, Krishnacharya G.

supporting information; experimental part, p. 9473 - 9475 (2009/04/06)

(Chemical Equation Presented) α,α-Disubstituted acetamides undergo oxidative dehomologation to give one-carbon-shorter ketones when reacted with a hypervalent iodine (λ5) reagent in combination with tetraethylammonium bromide (TEAB) in various solvents. In further studies, one such combination of a hypervalent iodine (λ5) reagent, o-iodoxybenzoic acid, and TEAB has been established as a new, mild, efficient, and general method for the transformation.

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