67901-82-0

Basic information

• Product Name: 7-HYDROXY-4-METHYL-1-INDANONE 97
• Synonyms: 7-HYDROXY-4-METHYL-1-INDANONE 97;4-Methyl-7-hydroxy-1-indanone;7-Hydroxy-4-Methyl-2,3-dihydro-1H-inden-1-one;4-Methyl-7-hydroxyindan-1-one;7-Hydroxy-4-methylindan-1-one;2,3-dihydro-7-hydroxy-4-methyl-1H-Inden-1-one;6-Hydroxy-2,3-dimethyl-benzaldehyde;7-Hydroxy-5-methyl-indan-1-one
• CAS NO: 67901-82-0
• Molecular Formula: C₁₀H₁₀O₂
• Molecular Weight: 162.187
• Product Categories: C10;Carbonyl Compounds;Ketones
• Mol File: 67901-82-0.mol
• Article Data: 5

Chemical Properties

• Melting Point: 109-112 °C(lit.)
• Boiling Point: 339.3 °C at 760 mmHg
• Flash Point: 144.4 °C
• Appearance: /
• Density: 1.25 g/cm³
• Vapor Pressure: 4.72E-05mmHg at 25°C
• Refractive Index: 1.614
• Storage Temp.: Inert atmosphere,Room Temperature
• PKA: 10.59±0.20(Predicted)
• CAS DataBase Reference: 7-HYDROXY-4-METHYL-1-INDANONE 97(CAS DataBase Reference)
• NIST Chemistry Reference: 7-HYDROXY-4-METHYL-1-INDANONE 97(67901-82-0)
• EPA Substance Registry System: 7-HYDROXY-4-METHYL-1-INDANONE 97(67901-82-0)

Safety Data

• Hazard Codes: Xn
• Statements: 22-36
• Safety Statements: 26
• WGK Germany: 2
• Hazardous Substances Data: 67901-82-0(Hazardous Substances Data)

Usage

General Description

7-HYDROXY-4-METHYL-1-INDANONE 97 is a chemical compound with the molecular formula C10H10O2. It is a white to off-white crystalline solid that is commonly used in the pharmaceutical industry as a building block for the synthesis of various drugs and pharmaceuticals. 7-HYDROXY-4-METHYL-1-INDANONE 97 is also used in the production of perfumes and flavors, as well as in the manufacturing of dyes and pigments. It is classified as a hazardous chemical and should be handled with care to avoid potential health risks.

InChI:InChI=1/C10H10O2/c1-6-2-4-8(11)10-7(6)3-5-9(10)12/h2,4,11H,3,5H2,1H3

Upstream product

• 68293-33-4 4-methylphenyl 2-bromopropanoate 
• 86260-02-8 4'-methylphenyl 3-bromopropionate 
• 106-44-5 p-cresol 
• 814-68-6 acryloyl chloride 
• 73057-23-5 3,7-dimethyl-1H-inden-4-ol 
• 104483-40-1 2,3-dihydro-1,4-dimethyl-1H-indene-1,7-diol 
• 13102-87-9 3-chloro-1-(2-hydroxy-5-methylphenyl)propan-1-one 
• 94102-85-9 4-methylphenyl-3-chloropropanoate 
• 137937-52-1 3-methylphenyl 2-chloropropanoate 
• 39513-75-2 6-methyl-4-chromanone 

Downstream Products

• 67901-83-1 2,3-dihydro-7-methoxy-4-methyl-1H-inden-1-one 
• 6339-84-0 7-(2-diethylamino-ethoxy)-4-methyl-indan-1-one; hydrochloride 
• 16400-13-8 7-methylindan-4-ol 

Relevant articles and documents

Structure-based drug design of tricyclic 8H-indeno[1,2-d][1,3]thiazoles as potent FBPase inhibitors

With the goal of improving metabolic stability and further enhancing FBPase inhibitory activity, a series of tricyclic 8H-indeno[1,2-d][1,3]thiazoles was designed and synthesized with the aid of structure-based drug design. Extensive SAR studies led to th

Anionic cyclizations of aromatic ester dithioacetals with facially biased α,β-unsaturated ketones

Cyclopent-2-enones bearing a plane-nonsymmetric oxygen function on C-4 reacted efficiently with anions derived from aromatic ester dithioacetals to provide annulated products in a highly diastereoselective fashion. Whereas the anion of a dimethoxy aromati

Synthetic Applications of Intramolecular Insertion in Arylcarbenes. VII. Aryl-Substituted Benzocycloalkenylidenes

A series of benzo-fused cyclic carbenes, bearing suitably located alkoxy substituents in the phenyl ring, has been generated in the gas phase and pyrolysed at 250 deg/0.002-0.40 mm.In all cases, carbene insertion into the adjacent C-H bond (Bamford-Stevens insertion) occurs, either exclusively or predominantly, with up to 35percent 1,5 C-H insertion in the alkoxy sidechain to form peri-fused tricyclic heterocycles.These results are rationalized in terms of geometrical and electronic effects.