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AI3-51930, also known as 2,6-dichloro-4-nitroaniline, is a yellow crystalline solid with a molecular formula of C6H4Cl2N2O2. It is a chemical compound that is commonly used in the production of dyes, pharmaceuticals, and agricultural chemicals. However, it is considered toxic and may cause skin irritation, eye damage, and harm if swallowed or inhaled. Therefore, it is classified as hazardous and should be handled with caution and proper safety measures.

2704-30-5

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2704-30-5 Usage

Uses

Used in Dye Industry:
AI3-51930 is used as a chemical intermediate for the production of various dyes. Its unique chemical structure allows it to be a key component in the synthesis of a wide range of dyes with different colors and properties.
Used in Pharmaceutical Industry:
AI3-51930 is used as a building block in the synthesis of certain pharmaceutical compounds. Its presence in the molecular structure of these compounds contributes to their therapeutic effects and medicinal properties.
Used in Agricultural Chemical Industry:
AI3-51930 is used in the production of agricultural chemicals, such as pesticides and herbicides. Its chemical properties make it effective in controlling pests and weeds, thereby protecting crops and increasing agricultural productivity.

Check Digit Verification of cas no

The CAS Registry Mumber 2704-30-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,0 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2704-30:
(6*2)+(5*7)+(4*0)+(3*4)+(2*3)+(1*0)=65
65 % 10 = 5
So 2704-30-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H7N3O3/c1-2(3(8)9)6-7-4(5)10/h1H3,(H,8,9)(H3,5,7,10)/b6-2+

2704-30-5SDS

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 (2E)-2-(carbamoylhydrazinylidene)propanoic acid

1.2 Other means of identification

Product number -
Other names isoamyl pyruvate

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:2704-30-5 SDS

2704-30-5Relevant academic research and scientific papers

Synthesis and antimicrobial evaluation of 6-azauracil non-nucleosides

El-Brollosy, Nasser R.

scheme or table, p. 1483 - 1490 (2009/12/26)

The present study describes synthesis and antimicrobial evaluation of a series of novel 6-azauracil non-nucleosides. Reaction of silylated 6-azauracils with the appropriate chloroethers gave the corresponding non-nucleosides. 1-(Allyloxymethy)-6-azauracils and non-nucleosides bearing indanyl, cyclohexenyl, and cyclohexyl moieties were obtained via silylation of 6-azauracils followed by treatment with the appropriate acetals. Selected compounds were tested for their in vitro antimicrobial activity against a panel of standard strains of Gram-positive and Gram-negative bacteria and the yeast-like pathogenic fungus Candida albicans. Four compounds showed marked inhibitory activity particularly against the tested Gram-positive bacteria.

MOESSBAUER STUDY OF IRON(II) AND IRON(III) COMPLEXES OF SOME NITROGEN-, OXYGEN- AND SULPHUR DONOR LIGANDS. REDUCTION OF IRON(III) BY THE MERCAPTIDE GROUP

Shawney, G. L.,Baijal, J. S.,Chandra, S.,Pandeya, K. B.

, p. 325 - 332 (2007/10/02)

Complex formation reactions of iron(II) and iron(III) with semicarbazones and thiosemicarbazones of pyruvic acid and phenyl pyruvic acid have been studied by magnetic measurements and Moessbauer spectroscopy.With iron(II) all the ligands form hexa-coordin

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