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1-(2-phenylhydrazinyl)heptose is a chemical compound with the molecular formula C20H30N2O5. It is a heptose derivative that contains a phenylhydrazine functional group. Heptose is a seven-carbon sugar derivative often found in bacterial lipopolysaccharides and plays a crucial role in the structure and function of these molecules. The addition of the phenylhydrazine group to heptose enhances its reactivity and potential biological activity.

6631-61-4

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6631-61-4 Usage

Uses

Used in Pharmaceutical Industry:
1-(2-phenylhydrazinyl)heptose is used as a building block for the synthesis of new drugs and biologically active molecules due to its enhanced reactivity and potential biological activity.
Used in Antimicrobial Applications:
1-(2-phenylhydrazinyl)heptose is used as an antimicrobial agent for the development of new antimicrobial agents, as studies have shown that it possesses antimicrobial properties.

Check Digit Verification of cas no

The CAS Registry Mumber 6631-61-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 1 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6631-61:
(6*6)+(5*6)+(4*3)+(3*1)+(2*6)+(1*1)=94
94 % 10 = 4
So 6631-61-4 is a valid CAS Registry Number.

6631-61-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,4,5,6,7-hexahydroxy-N'-phenylheptanehydrazide

1.2 Other means of identification

Product number -
Other names D-glycero-L-talo-heptonic acid-(N'-phenyl-hydrazide)

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:6631-61-4 SDS

6631-61-4Relevant academic research and scientific papers

Highly functionalised cyclopentanes by radical cyclisation of unsaturated bromolactones III. Preparation of carbaaldohexofuranoses. Determination of the relative configuration at C-4/C-5 of 2,3-unsaturated heptono-1,4-lactones by means of 1H NMR spectroscopy

Horneman, Anne Marie,Lundt, Inge

, p. 317 - 325 (2007/10/03)

Two new carbaaldohexofuranoses, carba-β-D-glucofuranose and carba-α- L-mannofuranose, have been prepared using 5,6-O-isopropylidene-D-glycero-L- galacto-heptono-1,4-lactone (6) as the starting material. The key step was a highly stereoselective intramolecular 5-exo-trig radical cyclisation of C-2 substituted 2,3-unsaturated 7-bromo-7-deoxyheptono-1,4-lactones promoted by tributyltin hydride. Assignment of the configuration of the unsaturated lactones was based upon NMR data of related compounds. The starting material, compound 6, was obtained by chain elongation of D-gulose, and a facile method for separation of the epimers from the chain elongation has been developed. Thus 5,6-O-isopropylidene-D-glycero-L-galacto-heptono-1,4-lactone (6) and D- glycero-L-taloheptono-1,4-lactone (5) were isolated crystalline in ca. 30% and 10% yield, respectively.

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