16644-30-7

Basic information

• Product Name: 3-CHLOROMETHYL-5-NITROSALICYLALDEHYDE
• Synonyms: Benzaldehyde,3-(chloroMethyl)-2-hydroxy-5-nitro-;3-chloromethyl-5-nitro-salicylaldehyd;3-CHLOROMETHYL-5-NITROSALICYLALDEHYDE;Chloromethylnitrosalicyaldehyde;3-CHLOROMETHYL-5-NITROSALICYLALDEHYDE 97+%;2-Hydroxy-3-(chloromethyl)-5-nitrobenzaldehyde;2-Hydroxy-3-chloromethyl-5-nitrobenzaldehyde;3-(Chloromethyl)-2-hydroxy-5-nitrobenzaldehyde
• CAS NO: 16644-30-7
• Molecular Formula: C₈H₆ClNO₄
• Molecular Weight: 215.59
• Mol File: 16644-30-7.mol
• Article Data: 12

Chemical Properties

• Melting Point: 92°C
• Boiling Point: 372.8°Cat760mmHg
• Flash Point: 179.3°C
• Appearance: /
• Density: 1.550±0.06 g/cm3 (20 ºC 760 Torr)
• Vapor Pressure: 4.37E-06mmHg at 25°C
• Refractive Index: 1.657
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 4.37±0.50(Predicted)
• CAS DataBase Reference: 3-CHLOROMETHYL-5-NITROSALICYLALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-CHLOROMETHYL-5-NITROSALICYLALDEHYDE(16644-30-7)
• EPA Substance Registry System: 3-CHLOROMETHYL-5-NITROSALICYLALDEHYDE(16644-30-7)

Safety Data

• RTECS: VN5500000
• Hazardous Substances Data: 16644-30-7(Hazardous Substances Data)

Usage

General Description

3-CHLOROMETHYL-5-NITROSALICYLALDEHYDE is a chemical compound that is commonly used in organic synthesis and pharmaceutical research. It is an aldehyde derivative with a chloromethyl group and a nitrosalicylaldehyde moiety, which gives it versatile reactivity and potential biological activity. 3-CHLOROMETHYL-5-NITROSALICYLALDEHYDE is often employed in the preparation of various organic compounds, including pharmaceutical intermediates, insecticides, and dyes. Its structural features make it a valuable building block for the creation of novel molecules with potential therapeutic applications. Additionally, it has been investigated for its antimicrobial and antioxidant properties, suggesting potential uses in medical and cosmetic formulations. Overall, 3-CHLOROMETHYL-5-NITROSALICYLALDEHYDE is a valuable compound with diverse applications in the fields of chemistry and biotechnology.

InChI:InChI=1/C8H6ClNO4/c9-3-5-1-7(10(13)14)2-6(4-11)8(5)12/h1-2,4,12H,3H2

Upstream product

• 97-51-8 5-Nitrosalicylaldehyde 
• 100-02-7 4-nitro-phenol 
• 107-30-2 chloromethyl methyl ether 

Downstream Products

• 141620-26-0 16-(3-formyl-2-hydroxy-5-nitrobenzyl)-1,4,7,10,13-pentaoxa-16-azacyclooctadecane 
• 420787-36-6 N-(2'-hydroxy-3'-formyl-5'-nitrobenzyl)-3,9-dithia-6-monoazaundecane 
• 288852-83-5 3-{[bis-(2-ethoxy-ethyl)-amino]-methyl}-2-hydroxy-5-nitro-benzaldehyde 
• 248936-95-0 2-hydroxy-5-nitro-3-(6,7,9,10,12,13,15,16-octahydro-5,8,14,17-tetraoxa-11-aza-benzocyclopentadecen-11-ylmethyl)-benzaldehyde 
• 141620-25-9 3-((1,4,7,10-tetraoxa-13-azacyclopentadecan-13-yl)methyl)-2-hydroxy-5-nitrobenzaldehyde 
• 82000-92-8 3-methacryloyloxymethyl-5-nitrosalicylaldehyde 
• 141620-24-8 10-(2-hydroxy-3-formyl-5-nitrobenzyl)-1,4,7-trioxa-10-azacyclododecane 
• 88253-65-0 3-<(dodecanoyloxy)methyl>-5-nitrosalicylaldehyde 
• 126062-55-3 3--5-nitrosalicylaldehyde 
• 141620-27-1 8-(3-formyl-2-hydroxy-5-nitrobenzyl)-2,5,11,14-tetraoxa-8-azapentadecane 
• 72462-30-7 8-chloromethyl-3',3'-dimethyl-6-nitro-1'-phenyl-1',3'-dihydro-spiro[chromene-2,2'-indole] 
• 1006591-00-9 C₂₈H₄₃N₃O₁₀ 
• 1006591-06-5 3-[N,N-bis(methoxycarbonylmethyl)aminomethyl]-5-nitrosalicylaldehyde 

Relevant articles and documents

The synthesis and spectroscopic properties of novel, photochromic indolinobenzospiropyran-based homopolymers prepared via ring-opening metathesis polymerization

Three types of novel photochromic indolinobenzospiropyran-based homopolymers were prepared via the ring-opening metathesis polymerization of the strained bicyclic indolinobenzospiropyran derivative. The homopolymers were soluble in common organic solvents and displayed unusually high polydispersity as determined by gel permeation chromatographic analysis. UV-visible absorption spectroscopy analysis in solution revealed that the appealing photochromic behaviour exhibited by the respective monomers was retained.

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