81995-32-6

Basic information

• Product Name: AKOS B014087
• Synonyms: AKOS B014087;CHEMBRDG-BB 3014087;ART-CHEM-BB B014087;TIMTEC-BB SBB009331;2-Isobutoxybenzaldehyde;2-isobutoxybenzaldehyde(SALTDATA: FREE);Benzaldehyde, 2-(2-Methylpropoxy)-;BAS 09975816
• CAS NO: 81995-32-6
• Molecular Formula: C₁₁H₁₄O₂
• Molecular Weight: 178.23
• Mol File: 81995-32-6.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 274.4°C at 760 mmHg
• Flash Point: 114.3°C
• Appearance: /
• Density: 1.018g/cm³
• Vapor Pressure: 0.00542mmHg at 25°C
• Refractive Index: 1.523
• CAS DataBase Reference: AKOS B014087(CAS DataBase Reference)
• NIST Chemistry Reference: AKOS B014087(81995-32-6)
• EPA Substance Registry System: AKOS B014087(81995-32-6)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 81995-32-6(Hazardous Substances Data)

Usage

General Description

AKOS B014087 is a chemical compound with the molecular formula C20H24O2. It is a synthetic organic compound that is used in various industrial and laboratory applications. It is a white to off-white solid with a melting point of 131-134°C and a boiling point of 401.9°C. AKOS B014087 is commonly used as an intermediate in the synthesis of other organic compounds and is also used as a reagent in chemical reactions. It is important to handle AKOS B014087 with care as it may pose health and environmental hazards if not properly managed.

InChI:InChI=1/C11H14O2/c1-9(2)8-13-11-6-4-3-5-10(11)7-12/h3-7,9H,8H2,1-2H3

Upstream product

• 78-77-3 Isobutyl bromide 
• 90-02-8 salicylaldehyde 
• 563-47-3 3-Chloro-2-methylpropene 
• 513-38-2 Isobutyl iodide 

Downstream Products

• 944419-51-6 (2-isobutoxyphenyl)N,N-dimethylmethanamine 
• 944419-74-3 (E)-benzyl 3-(3-butoxy-2-((dimethylamino)methyl)phenyl)acrylate 
• 467252-18-2 3-(3-isobutoxy-2-methylphenyl)propanoic acid 
• 21315-20-8 2-isobutoxyphenol 
• 1179356-18-3 3-[2-(2-methylpropoxy)benzyl]-9-(pyridin-4-ylcarbonyl)-3,9-diazaspiro[5.5]undecane trifluoroacetate 
• 1517-59-5 (R)-o-methylbenzhydrol 
• 1517-59-5 2-methyl-(S)-benzhydrol 

Relevant articles and documents

Pyridopyril compound and medical application thereof

The invention relates to a pyridine ring compound and a medical application thereof as shown in a formula (I). The invention further relates to a preparation method of the compound. Use of a pharmaceutical composition and as FGFR4 inhibitor for the treatment of cancer.

Chiral Lithium Amido Zincates for Enantioselective 1,2-Additions: Auto-assembling Reagents Involving a Fully Recyclable Ligand

A methodology consisting in carrying out enantioselective nucleophilic 1,2-additions (ee values up to 97 %) from cheap, easily accessible, and never described before, chiral lithium amido zincates is presented. These multicomponent reactants auto-assemble when mixing, in a 1:1 ratio, a homoleptic diorganozinc (R2Zn) with a chiral lithium amide (CLA). The latter, obtained after a single reductive amination, plays the role of the chiral inductor and is fully recoverable thanks to a simple acid–base wash, allowing being recycled and re-use without loss of stereochemical information.

Probing solvent effects on mixed aggregates associating a chiral lithium amide and n-BuLi by NMR: From structure to reactivity

An NMR study of a 1 : 1 mixture of a chiral lithium amide (4a) and n-BuLi shows that depending on the solvent employed (Et2O or THF) a mixed aggregate can form in proportions that are directly related to the ees measured during the enantioselec