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1709-44-0

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1709-44-0 Usage

Description

3-Aminobenzaldehyde Polymer is a light brown powdery crystal with a melting point of 28-30°C. It is soluble in ether and quickly decomposes into brown resin in the presence of a small amount of water. This polymer is an intermediate in organic synthesis, making it a valuable component in the production of various chemical compounds.

Uses

Used in Organic Synthesis:
3-Aminobenzaldehyde Polymer is used as an intermediate in organic synthesis for the production of various chemical compounds. Its unique chemical properties and reactivity make it a versatile building block in the synthesis of pharmaceuticals, dyes, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-Aminobenzaldehyde Polymer is used as a key intermediate in the synthesis of various drugs and drug candidates. Its ability to form a wide range of chemical bonds and its compatibility with other organic compounds make it an essential component in the development of new medications.
Used in Dye Industry:
3-Aminobenzaldehyde Polymer is used as a precursor in the production of dyes and pigments. Its chemical structure allows for the creation of a variety of colorants, making it a valuable resource in the dye industry.
Used in Specialty Chemicals:
3-Aminobenzaldehyde Polymer is also used in the production of specialty chemicals, such as agrochemicals, fragrances, and flavorings. Its versatility and reactivity contribute to the development of unique and innovative products in these industries.

Synthesis

3-AMINOBENZALDEHYDE POLYMER uses m-nitrobenzaldehyde as raw material, and is reduced with sodium disulfide, or reduced with sodium bisulfite and ferrous sulfate.

Check Digit Verification of cas no

The CAS Registry Mumber 1709-44-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,0 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1709-44:
(6*1)+(5*7)+(4*0)+(3*9)+(2*4)+(1*4)=80
80 % 10 = 0
So 1709-44-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H7NO/c8-7-3-1-2-6(4-7)5-9/h1-5H,8H2

1709-44-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-AMINOBENZALDEHYDE POLYMER

1.2 Other means of identification

Product number -
Other names Benzaldehyde, 3-amino-

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:1709-44-0 SDS

1709-44-0Relevant articles and documents

Selective hydrogenation of nitroarenes over MOF-derived Co@CN catalysts at mild conditions

Hu, Ao,Lu, Xinhuan,Cai, Dongming,Pan, Haijun,Jing, Run,Xia, Qinghua,Zhou, Dan,Xia, Yongde

, p. 27 - 36 (2019)

N-doped porous carbons incorporating highly-dispersed non-noble metallic cobalt (Co) nanoparticle materials were synthesized by rapid pyrolysis of a zeolitic-type metal-organic framework (ZIF-9) and their structures, morphologies, topologies and relevant physical and chemical properties were fully measured by different characterization technologies. The resulting derived Co/CN materials were further evaluated as catalysts in nitrobenzene hydrogenation. It was found that Co/CN materials showed remarkbly catalytic activity and chemoselectivity for mild hydrogenation of nitrobenzene. Amongst the studied a series of Co/CN-x (pyrolyzed at x °C) materials, sample Co@CN-800 shows the most superior catalytic activity for hydrogenation of nitrobenzene. In particular, the catalytic conversion activity of Co@CN-800 is 100% with aniline being the sole product at 70 °C for 2 h, 27.5 times higher than that of cobalt powder (Co). It is believed that the large pore size, adsorption of nitroarenes substrate with high selectivity and strong interaction of Co nanoparticles with the doped N species can result in the high activity of Co@CN-800. This work therefore offers a cost-effective approach in developing highly efficient catalytic materials towards mild hydrogenation of nitrobenzene.

Silver nanoparticles supported on P, Se-codoped g-C3N4 nanosheet as a novel heterogeneous catalyst for reduction of nitroaromatics to their corresponding amines

Elhampour, Ali,Heravi, Majid M.,Nemati, Firouzeh,Piri, Mohadese

, (2021/06/21)

P, Se-codoped g-C3N4 (PSeCN) nanosheet was in situ prepared by facile thermal polymerization of melamine, phosphonitrilic chloride trimer, and selenium black powder as the precursors. It was found as a suitable support for the immobilization of silver nanoparticles (Ag NPs). The prepared nanocatalyst was fully characterized via standard analysis methods including EDX, ICP-OES, XRD, FT-IR, SEM, TEM, and BET. This PSeCN/Ag nanocatalyst with a higher specific surface area compared with CN, showed excellent catalytic activity towards the reduction of several nitroaromatic compounds using sodium borohydride (NaBH4) in short reaction times with high efficiency and good selectivity in water as a green solvent. Significantly, the above-mentioned nanocomposite could be reused six times without appreciable loss of its catalytic activity.

Cobalt oxide NPs immobilized on environmentally benign biological macromolecule-derived N-doped mesoporous carbon as an efficient catalyst for hydrogenation of nitroarenes

Elhampour, Ali,Nanadegani, Zahra Soleimani,Nemati, Firouzeh,Rangraz, Yalda

, (2020/09/15)

Highly nitrogen-doped mesoporous carbon (N-mC) material incorporated cobalt oxide nanoparticles was synthesized through simple pyrolysis of environmentally friendly chitosan-polyaniline-Co(OAc)2 precursor in one-step. The as-prepared catalyst named CoO&at;N-mC with 14.65 ?wtpercent nitrogen content was characterized by different analysis techniques. The heterogeneous catalyst exhibits outstanding catalytic activity for the reduction of a variety of nitroaromatic compounds in the presence of NaBH4 as a reducing agent in water as a green solvent at 75 ?°C. Utilization of natural biological macromolecules such as chitosan as green and cheap starting material with harmless aniline and earth-abundant cobalt salt, facile synthesis, excellent product yield, short reaction time, high chemoselectivity, sustainable and mild reaction condition, and reusability of catalyst for at least five cycles without any significant decline in the catalytic efficiency are some prominent merits of this new nanocatalyst.

Chemoselective reduction of nitro and nitrile compounds using an Fe3O4-MWCNTs?PEI-Ag nanocomposite as a reusable catalyst

Ansari, Sara,Khorshidi, Alireza,Shariati, Shahab

, p. 3554 - 3565 (2020/02/04)

Multi-walled carbon nanotubes (MWNTs) were modified with carboxylic acid functional groups (MWCNTs-(COOH)n) prior to decoration with Fe3O4 nanoparticles. A further modification step by polyethyleneimine (PEI) resulted in Fe3O4-MWCNTs?PEI which provided a suitable platform for coordination and in situ reduction of silver ions to obtain an Fe3O4-MWCNTs?PEI-Ag nanocomposite with highly dispersed Ag nanoparticles. The Fe3O4-MWCNTs?PEI-Ag hybrid material was characterized by various techniques such as Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), transmission electron microscopy (TEM), vibrating sample magnetometry (VSM), X-ray photoelectron spectroscopy (XPS) and thermogravimetric analysis (TGA), and was used as an efficient catalyst for chemoselective reduction of nitroaromatic and nitrile compounds to their corresponding amines in aqueous solution at ambient temperature. Nitrofurazone, a cytotoxic antibiotic, as a non-aromatic example was also reduced selectively at the nitro group without reduction of the other functionalities in the presence of Fe3O4-MWCNTs?PEI-Ag. The catalyst was magnetically recoverable and maintained its activity for at least six cycles without considerable loss of efficiency.

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