31680-07-6

Basic information

• Product Name: 4-METHYL-3-NITROBENZALDEHYDE
• Synonyms: Methylnitrobenzaldehyde;4-Methyl-3-nitrobenzaldehyde,98%;4-Methyl-3-nitrobenzaldehyde 98%;4-Formyl-2-nitrotoluene, 3-Nitro-p-tolualdehyde;4-Methyl-3-nitrobenzaldehyde, 95%+;RARECHEM AH CK 0134;ASISCHEM R42201;4-METHYL-3-NITROBENZALDEHYDE
• CAS NO: 31680-07-6
• Molecular Formula: C₈H₇NO₃
• Molecular Weight: 165.15
• EINECS: 250-760-4
• Product Categories: Aromatic Aldehydes & Derivatives (substituted);Benzaldehyde;Aldehydes;C8;Carbonyl Compounds
• Mol File: 31680-07-6.mol
• Article Data: 10

Chemical Properties

• Melting Point: 46-49 °C(lit.)
• Boiling Point: 276℃
• Flash Point: >230 °F
• Appearance: Yellow crystalline powder
• Density: 1.278
• Vapor Pressure: 0.00485mmHg at 25°C
• Refractive Index: 1.602
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• Water Solubility: Insoluble in water.
• Sensitive: Air Sensitive
• BRN: 1637706
• CAS DataBase Reference: 4-METHYL-3-NITROBENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-METHYL-3-NITROBENZALDEHYDE(31680-07-6)
• EPA Substance Registry System: 4-METHYL-3-NITROBENZALDEHYDE(31680-07-6)

Safety Data

• Hazard Codes: Xi,Xn
• Statements: 36/37/38-22
• Safety Statements: 26-36/37/39-37/39
• WGK Germany: 3
• Hazardous Substances Data: 31680-07-6(Hazardous Substances Data)

Usage

Chemical Properties

Yellow crystalline powder

Uses

4-Methyl-3-nitrobenzaldehyde is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff.

InChI:InChI=1/C8H7NO3/c1-6-2-3-7(5-10)4-8(6)9(11)12/h2-5H,1H3

Upstream product

• 106-42-3 para-xylene 
• 104-87-0 4-methyl-benzaldehyde 
• 7664-93-9 sulfuric acid 
• 7697-37-2 nitric acid 
• 96-98-0 4-methyl-3-nitrobenzoic acid 
• 541-41-3 chloroformic acid ethyl ester 
• 108-88-3 toluene 
• 40870-59-5 (4-Methyl-3-nitro-phenyl)-methanol 

Downstream Products

• 127791-55-3 3-nitro-4-methyl-trans-cinnamic acid 
• 107151-66-6 4,4'-dimethyl-3,3'-dinitro-trans-chalcone 
• 96-98-0 4-methyl-3-nitrobenzoic acid 
• 57295-30-4 3-hydroxy-4-methylbenzaldehyde 
• 40870-59-5 (4-Methyl-3-nitro-phenyl)-methanol 
• 35781-34-1 4-methyl-3-nitro-cinnamic acid 
• 132390-58-0 4-methyl-3-nitro-chalcone 
• 32989-68-7 trans-4-(β-dimethylaminovinyl)-3-nitrobenzaldehyde 
• 939-79-7 4-cyano-2-nitrotoluene 

Relevant articles and documents

Diarylurea-linked zinc porphyrin dimer as a dual-mode artificial receptor: Supramolecular control of complexation-facilitated photoinduced electron transfer

A novel porphyrinic receptor 1 in which two zinc porphyrins are bridged by two diarylurea linkers was developed for recognition of a viologen derivative (hexyl viologen, HV). The electronic absorption spectra as well as the 1H NMR experiments revealed that the HV molecule was bound to the cleft in 1 mainly through carbonyl dipole-charge interactions to afford a 1:1 complex. From the steady-state fluorescence spectroscopic study, the photoinduced electron transfer (PET) from 1 to HV was extremely facilitated by the receptor-substrate complexation. The receptor 1 also formed a 1:1 complex with 1,4-diazabicyclo[2.2.2]octane (DABCO) through two Zn-N coordination interactions, and, using DABCO as an inhibitor, we suppressed the PET reaction via the substrate exchange. Copyright

INSECTICIDAL ARYL ISOXAZOLINE DERIVATIVES

The present invention relates to novel aryl isoxazoline derivatives having excellent insecticidal activity as insecticides and represented by the formula: and their use as insecticides and acarizides.

Synthesis and structure-activity relationships of 2-(substituted phenyl)-3-[3-(N,N-dimethylamino)propyl]-1,3-thiazolidin-4-ones acting as H1-histamine antagonists

2-(Substituted-phenyl)-3-[3-(N,N-dimethylamino)propyl]-1,3-thiazolidin-4-ones (1-15) showed dependence of the potency of the H1-histamine antagonism on the m- and p-substituents suggesting that the aromatic moiety binds the receptor by a strong