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3-nitro-N-phenyl-benzimidoyl chloride is an organic chemical compound with the molecular formula C13H8ClN3O3. It is a derivative of benzimidoyl chloride, featuring a nitro group at the 3-position and a phenyl group attached to the nitrogen atom. 3-nitro-N-phenyl-benzimidoyl chloride is often used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds due to its reactive imidoyl chloride group. It is typically synthesized through the reaction of 3-nitro-N-phenylaniline with phosgene or a similar reagent. The compound is sensitive to moisture and should be handled under anhydrous conditions to prevent hydrolysis. Its reactivity makes it a valuable building block in organic synthesis, particularly for the preparation of amides and other nitrogen-containing compounds.

5509-90-0

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5509-90-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5509-90-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,0 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5509-90:
(6*5)+(5*5)+(4*0)+(3*9)+(2*9)+(1*0)=100
100 % 10 = 0
So 5509-90-0 is a valid CAS Registry Number.

5509-90-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-nitro-N-phenyl-benzimidoyl chloride

1.2 Other means of identification

Product number -
Other names 3-Nitro-N-phenyl-benzimidoylchlorid

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:5509-90-0 SDS

5509-90-0Upstream product

5509-90-0Relevant academic research and scientific papers

Preparation of 1,5-disubstituted tetrazoles under phase-transfer conditions

Artamonova,Zhivich,Dubinskii,Koldobskii

, p. 1428 - 1430 (2007/10/03)

Imidoyl chlorides, obtained by common methods from a wide range of aromatic mono- and diamides, are smoothly converted to the corresponding tetrazoles in high yields by treatment with NaN3 under phase-transfer conditions.

Syntheses and basicity of 4-(N,N-dimethylamino)-2-arylquinazolines

Zielinski, Wojciech,Kudelko, Agnieszka,Holt, Elizabeth M.

, p. 1201 - 1209 (2007/10/03)

The reaction of substituted N-phenylbenzimidoyl chlorides with N,N-dimethylcyanamide in the presence of titanium tetrachloride has yielded seven 4-(N,N-dimethylamino)-2-arylquinazolines substituted on the phenyl ring with electron donating or withdrawing groups. pKa values have been determined for these compounds and analyzed in conjunction with the Hammertt σ constants to observe the influence of these phenyl substituents upon the basicity of 4-(N,N-dimemylamino)-2-arylquinazolines. The σ value, single crystal X-ray analysis and 15N-nmr spectra give evidence about the preferential site of protonation in such systems.

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