39750-93-1

Basic information

• Product Name: 2-ADAMANTANECARBOXZALDEHYDE
• Synonyms: 2-ADAMANTANECARBOXZALDEHYDE;2-adaMantanecarboxaldehyde;2-Formyladamantane;Tricyclo[3.3.1.1(3,7)]decane-2-carboxaldehyde;tricyclo[3.3.1.13,7]decane-2-carbaldehyde;AdaMantane-2-carbaldehyde
• CAS NO: 39750-93-1
• Molecular Formula: C₁₁H₁₆O
• Molecular Weight: 164.24414
• Mol File: 39750-93-1.mol
• Article Data: 19

Chemical Properties

• Melting Point: 158-160℃
• Boiling Point: 247.5±9.0℃ (760 Torr)
• Flash Point: 85.5±11.2℃
• Appearance: /
• Density: 1.124±0.06 g/cm3 (20 ºC 760 Torr)
• CAS DataBase Reference: 2-ADAMANTANECARBOXZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-ADAMANTANECARBOXZALDEHYDE(39750-93-1)
• EPA Substance Registry System: 2-ADAMANTANECARBOXZALDEHYDE(39750-93-1)

Safety Data

• Hazardous Substances Data: 39750-93-1(Hazardous Substances Data)

Usage

Uses

Adamantane-2-carbaldehyde can be used to treat tuberculosis.

InChI:InChI=1S/C11H16O/c12-6-11-9-2-7-1-8(4-9)5-10(11)3-7/h6-11H,1-5H2

Upstream product

• 24759-97-5 2-adamantanespiroxirane 
• 1826-67-1 vinyl magnesium bromide 
• 875-72-9 2-methylideneadamantane 
• 22635-61-6 ((1r,3r,5r,7r)-adamantan-2-yl)methanol 
• 68251-94-5 ω-(Bromomethylene)adamantane 
• 53082-05-6 2-Hydroxy-2-isopropylmethyladamantan 
• 700-58-3 2-Adamantanone 
• 63830-94-4 Adamantan-2-oxiran-3-ylmethyltrimethylsilane 
• 35856-00-9 2-adamantanecarbonitrile 
• 110166-53-5 2-Adamantan-2-yl-benzo[1,3]dithiole 
• 84454-51-3 diethylmethyl<(tricyclo<3.3.1.1^3,7>decylidene)methoxy>silane 
• 111922-77-1 2-Isocyanomethylene-adamantane 
• 72590-63-7 2-(methoxymethylene)adamantane 
• 412346-92-0 tert.-Butyl-epoxyadamantylidenacetat 

Downstream Products

• 76527-56-5 2-(N-Methylanilinomethylene)adamantane 
• 15897-81-1 adamantane-2-carboxylic acid 
• 1027925-93-4 adamantan-2-yl-(4-fluoro-phenyl)-methanol 
• 151386-39-9 2-(adamant-2-ylmethyl)aminodiphenylamine 
• 53140-72-0 2-adamantyl(phenyl)methanol 
• 68157-27-7 adamantan-2-yl(phenyl)methanone 
• 219812-03-0 2-benzoyl-2-methyladamantane 
• 219812-02-9 2-(p-fluorobenzoyl)adamantane 
• 219812-04-1 2-(p-fluorobenzoyl)-2-methyladamantane 
• 314041-56-0 2-Benzoyl-adamantane-2-carboxylic acid (S)-2-methyl-butyl ester 
• 479415-86-6 Adamantane-2-carboxylic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester 
• 314041-51-5 2-Benzoyl-adamantane-2-carboxylic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester 
• 151620-70-1 1-N-(adamant-2-ylmethyl)-3-amino-2,4-dioxo-5-N-phenyl-2,3,4,5-tetrahydro-1H-1,5-benzodiazepine 
• 151386-40-2 1-(adamant-2-ylmethyl)-2,4-dioxo-5-phenyl-3-phenylhydrazono-2,3,4,5-tetrahydro-1H-1,5-benzodiazepine 

Relevant articles and documents

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Photochemical Homologation for the Preparation of Aliphatic Aldehydes in Flow

Cheap and readily available aqueous formaldehyde was used as a formylating reagent in a homologation reaction with nonstabilized diazo compounds, enabled by UV photolysis of bench-stable oxadiazolines in a flow photoreactor. Various aliphatic aldehydes were synthesized along with the corresponding derivatized alcohols and benzimidazoles. No transition-metal catalyst or additive was required to affect the reaction, which proceeded at room temperature in 80 min.

Ring-fused compound, pharmaceutical composition containing same and application of compound

The invention discloses a ring-fused compound, a preparation method thereof, pharmaceutical composition containing the compound and an application of the compound. A polycyclic compound (I) as well asan isomer, a prodrug, a stable isotopic derivative or pharmacologically acceptable salt of the compound (I) has the following structure. The polycyclic compound has good IDO1 and/or TDO2 inhibition functions, can effectively treat, relieve and/or prevent various diseases which are related with IDO1 and/or TDO2, such as cancer, virus infection, autoimmune diseases or the like.