Welcome to LookChem.com Sign In|Join Free
  • or
Glutaranilide is a synthetic chemical compound with the molecular formula C10H12N2O3. It is a derivative of glutaric anhydride and aniline, and is known for its potential use as a pharmaceutical intermediate. Glutaranilide has been studied for its potential applications in the development of new drugs, particularly in the area of central nervous system medications. Glutaranilide's structure allows it to interact with certain receptors in the body, which could make it a candidate for treating various conditions. However, it is important to note that while glutaranilide has shown promise in preliminary research, it is not currently an approved medication and further studies are needed to fully understand its safety and efficacy.

6833-02-9

Post Buying Request

6833-02-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

6833-02-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6833-02-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,3 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6833-02:
(6*6)+(5*8)+(4*3)+(3*3)+(2*0)+(1*2)=99
99 % 10 = 9
So 6833-02-9 is a valid CAS Registry Number.

6833-02-9SDS

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 N,N'-diphenylpentanediamide

1.2 Other means of identification

Product number -
Other names Glutarsaeure-dianilid

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:6833-02-9 SDS

6833-02-9Relevant academic research and scientific papers

Synthesis of N,N′-diarylalkanediamides and their antimycobacterial and antialgal activity

Kubicova, Lenka,Waisser, Karel,Kunes, Jiri,Kralova, Katarina,Odlerova, Zelmira,Slosarek, Milan,Janota, Jiri,Svoboda, Zbynek

, p. 714 - 726 (2007/10/03)

A set of N,N′-diarylalkanediamides was synthesized. The compounds were tested for their antimycobacterial and antialgal activity. The antimycobacterial activity of N,N′-diarylalkanediamides depends on the lipophilicity of the respective acid. Antimycobacteri-ally active substances were found only in the series of N,N′-diarylethanediamides and N,N′-diarylbutanediamides. Other compounds (derivatives of pentane-, hexane-, octane- and nonanediamide) were inactive against various strains of mycobacteria. The compounds inhibited growth and chlorophyll production in Chlorella vulgaris. Their relatively low antial-gal activity is probably connected with their lowered aqueous solubility, and hence by a restricted passage of the inhibitor through the hydrophilic regions of thylakoid membranes.

A convenient acylation procedure of alcohols and amines

Misharin,Chernov

, p. 616 - 620 (2007/10/03)

The reaction of carboxylic acids with primary and secondary alcohols in the presence of aromatic sulfochlorides (mesitylenesulfonyl chloride and 2,4,6-triisopropylbenzenesulfonyl chloride) or aromatic sulfotetrazoles (mesytilenesulfonyl tetrazolide and 2,4,6-triisopropylbenzenesulfonyltetrazole) and usual acylation catalysts was shown to be a convenient procedure for the synthesis of esters. Reaction of carboxylic acids with primary aliphatic or aromatic amines in the presence of the same tetrazolides and catalysts is a useful procedure for the synthesis of amides. Syntheses of twenty compounds are presented as examples.

SYNTHESIS AND REACTIONS OF N-(p-CHLOROSULPHONYLPHENYL)-SUCCINIMIDE, -GLUTARIMIDE AND -CAMPHORIMIDE

Cremlyn, Richard,Nunes, Ricardo

, p. 183 - 186 (2007/10/02)

N-Phenyl-succinimide, -glutarimide and -camphorimide mreact with chlorosulphonic acid to yield the corresponding sulphonyl chlorides.Condensation with nucleophiles afforded 25 sulphonyl derivatives, which are to be examined for biocidal properties. reacti

Reaction of Phenyl Isothiocyanate with Some α,N-Acylamino and Dicarboxylic Acids

Ashare, Ram,Ram, Ram N.,Mukerjee, Arya K.

, p. 759 - 760 (2007/10/02)

Dianilides are obtained in the reaction of phenyl isothiocyanate with dicarboxylic acids, such as oxalic, malonic, glutaric and adipic acids, and not in the case of succinic and phthalic acids.In the case of succinic acid, the product is monoanilide, dianilide or N-phenylsuccinimide, depending upon the reaction conditions.Phthalic acid always gives N-phenylphthalimide.N-Acylamino acids on reaction with phenyl isothiocyanate yield the corresponding anilides.The probable mechanisms of this reaction are discussed.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 6833-02-9