95537-93-2

Basic information

• Product Name: ANISALDEHYDE-[7-13C]
• Synonyms: ANISALDEHYDE-[7-13C];4-Anisaldehyde-13C;4-Methoxybenzaldehyde-13C;Anisaldehyde-13C;Anisic Aldehyde-13C;Aubepine-13C;Crategine-13C;NSC 5590-13C
• CAS NO: 95537-93-2
• Molecular Formula: C₈H₈O₂
• Molecular Weight: 136.14792
• Product Categories: Aromatics Compounds;Aromatics;Isotope Labeled Compounds;Isotope Labelled Compounds
• Mol File: 95537-93-2.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• Density: 1.088g/cm3
• Refractive Index: 1.547
• Storage Temp.: -20?C Freezer
• Solubility: Chloroform (Slightly), Methanol (Slightly)
• CAS DataBase Reference: ANISALDEHYDE-[7-13C](CAS DataBase Reference)
• NIST Chemistry Reference: ANISALDEHYDE-[7-13C](95537-93-2)
• EPA Substance Registry System: ANISALDEHYDE-[7-13C](95537-93-2)

Safety Data

• Hazardous Substances Data: 95537-93-2(Hazardous Substances Data)

Usage

Chemical Properties

ANISALDEHYDE-[7-13C] is Colourless Oil

Uses

ANISALDEHYDE-[7-13C] is a metabolic product of the odoriferous fungus Lentinus lepidus. Anisaldehyde is used in perfumery and toilet soaps.

InChI:InChI=1/C8H8O2/c1-10-8-4-2-7(6-9)3-5-8/h2-6H,1H3/i6+1

Upstream product

• 76104-36-4 4-methoxy-<7-13C>benzyl alcohol 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 32488-43-0 N,N-dimethylform-¹³C-amide 
• 69838-89-7 4-methoxy-<7-13C>benzoic acid 
• 93627-95-3 methyl 4-methoxy-<7-13C>benzoate 
• 1333245-00-3 (¹³C)-4-methoxybenzonitrile 
• 696-62-8 para-iodoanisole 
• 3228-27-1 [13C]-formaldehyde 
• 874-90-8 4-methoxybenzonitrile 

Downstream Products

• 152404-52-9 4-hydroxy-<7-13C>benzaldehyde 
• 93627-97-5 C₇⁽¹³⁾CH₉BrO 
• 32345-64-5 1-(4-methoxyphenyl) ethane-1,2-diol 
• 648934-25-2 C₁₁⁽¹³⁾CH₁₉O₄P 
• 1229516-39-5 3-(4-methoxyphenyl)-1-[2,4-bis(benzyloxy)phenyl]-2-[1,2,3-⁽¹³⁾C₃]propen-1-one 
• 1229516-40-8 3-(4-methoxyphenyl)-1-[2,4,6-tris(benzyloxy)phenyl]-[1,2,3-⁽¹³⁾C₃]-2-propen-1-one 
• 1229516-27-1 1-(2-acetoxy-4-methoxyphenyl)-3-(4-methoxyphenyl)[1,2,3-⁽¹³⁾C₃]prop-2-en-1-one 
• 1229516-33-9 1-(2-hydroxy-4-methoxyphenyl)-3-(4-methoxyphenyl)[1,2,3-⁽¹³⁾C₃]prop-2-en-1-one 
• 1229516-34-0 C₁₅⁽¹³⁾C₃H₁₈O₅ 
• 1229516-35-1 3-(4-methoxyphenyl)-1-[2-acetoxy-4,6-dimethoxyphenyl]-2-[1,2,3-⁽¹³⁾C₃]propen-1-one 
• 957199-29-0 [2,3,4-⁽¹³⁾C₃]formononetin 
• 957199-28-9 [2,3,4-⁽¹³⁾C₃]biochanin A 
• 1453504-05-6 (¹³C)-1-(2,2-dibromovinyl)-4-methoxybenzene 
• 1333245-00-3 (¹³C)-4-methoxybenzonitrile 

Relevant articles and documents

Direct Carbon Isotope Exchange of Pharmaceuticals via Reversible Decyanation

The incorporation of carbon-14 allows tracking of organic molecules and provides vital knowledge on their fate. This information is critical in pharmaceutical development, crop science, and human food safety evaluation. Herein, a transition-metal-catalyzed procedure enabling carbon isotope exchange on aromatic nitriles is described. By utilizing the radiolabeled precursor Zn([14C]CN)2, this protocol allows the insertion of the desired carbon tag without the need for structural modifications, in a single step. By reducing synthetic costs and limiting the generation of radioactive waste, this procedure will facilitate the labeling of nitrile containing drugs and accelerate 14C-based ADME studies supporting drug development.

Nickel-catalyzed decarbonylative alkylidenation of phthalimides with trimethylsilyl-substituted alkynes

We have developed a nickel-catalyzed transformation, in which phthalimides react with trimethylsilyl-substituted alkynes in the presence of Ni(0)/PMe 3/MAD catalyst to provide isoindolinones. The reaction process displays an unusual mechanistic

Ruthenium-Catalyzed Aromatization of Aromatic Enynes via the 1,2-Migration of Halo and Aryl Groups: A New Process Involving Electrocyclization and Skeletal Rearrangement

-