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646483-08-1

4-Hydroxy-5-methyl-5-octylthiophen-2(5H)-one is a complex organic compound with the molecular formula C13H22OS. It is a derivative of thiophene, a heterocyclic compound with a sulfur atom in the ring. This specific compound features a hydroxyl group (-OH) at the 4-position, a methyl group (-CH3) at the 5-position, and an octyl chain (C8H17) attached to the sulfur atom. The compound is characterized by its unique chemical structure, which may contribute to its potential applications in various fields, such as pharmaceuticals, agrochemicals, or materials science. Due to its specific functional groups and molecular structure, it may exhibit unique chemical properties and reactivity, making it a subject of interest for researchers and chemists.

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  • 646483-08-1 Structure

  • Basic information

    1. Product Name: 4-hydroxy-5-Methyl-5-octylthiophen-2(5H)-one
    2. Synonyms: 4-hydroxy-5-Methyl-5-octylthiophen-2(5H)-one;PIRZFZMRZHTILE-UHFFFAOYSA-N
    3. CAS NO:646483-08-1
    4. Molecular Formula: C13H22O2S
    5. Molecular Weight: 242.37758
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 646483-08-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 353.5±42.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.063±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 4.50±1.00(Predicted)
    10. CAS DataBase Reference: 4-hydroxy-5-Methyl-5-octylthiophen-2(5H)-one(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-hydroxy-5-Methyl-5-octylthiophen-2(5H)-one(646483-08-1)
    12. EPA Substance Registry System: 4-hydroxy-5-Methyl-5-octylthiophen-2(5H)-one(646483-08-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 646483-08-1(Hazardous Substances Data)

646483-08-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 646483-08-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,6,4,8 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 646483-08:
(8*6)+(7*4)+(6*6)+(5*4)+(4*8)+(3*3)+(2*0)+(1*8)=181
181 % 10 = 1
So 646483-08-1 is a valid CAS Registry Number.

646483-08-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-hydroxy-2-methyl-2-octylthiophen-3-one

1.2 Other means of identification

Product number -
Other names 2(5H)-Thiophenone,4-hydroxy-5-methyl-5-octyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:646483-08-1 SDS

646483-08-1Relevant articles and documents

Application of a flexible synthesis of (5R)-thiolactomycin to develop new inhibitors of type I fatty acid synthase

McFadden, Jill M.,Medghalchi, Susan M.,Thupari, Jagan N.,Pinn, Michael L.,Vadlamudi, Aravinda,Miller, Katherine I.,Kuhajda, Francis P.,Townsend, Craig A.

, p. 946 - 961 (2005)

Fatty acid synthase (FAS) catalyzes the synthesis of palmitate from the sequential condensation of an acetyl primer with two carbon units added from malonyl-CoA. Inhibition of the β-ketoacyl synthase domain of mammalian FAS leads to selective cytotoxicity

NOVEL COMPOUNDS, PHARMACEUTICAL COMPOSITIONS CONTAINING SAME, AND METHODS OF USE FOR SAME

-

, (2009/12/28)

The class compounds of the present invention may be represented by Formula (I), wherein X may be O, S, or N. R1 and R2 are independently either H, C1-C20 alkyl, cycloalkyl, alkenyl, aryl, arylalkyl, or alkylaryl

NOVEL COMPOUNDS, PHARMACEUTICAL COMPOSITIONS CONTAINING SAME, AND METHODS OF USE FOR SAME

-

, (2008/12/05)

Compounds having the following general formula, pharmaceutical compositions comprising the compounds, and methods of treating cancer, obesity, and microbial infections using such compositions: wherein: R1 = H, C1-C20 alkyl, cycloalkyl, alkenyl, aryl, aryl

NOVEL COMPUNDS, PHARMACEUTICAL COMPOSITIONS CONTAINING SAME, AND METHODS OF USE FOR SAME

-

Page 29, (2010/02/06)

A pharmaceutical composition comprising a phamaceurtical diluent and a compound of formula IV wherein R21= H, C1-C20 alkyl, cycloalkyl, alkenyl, aryl, arylalkyl, or alkylaryl, -CH2OR25, -C(O)R25, -CO(O)R25, -C(O)NR25R26, -CH2C(O)R25, or -CH2C(O)NHR25, where R25 and R26 are each independently H, C1-C10 alkyl, cycloalkyl, alkenyl, aryl, arylalkyl, or alkylaryl, optionally containing one or more halogen atoms. R22 = -OH, -OR27, -OCH2C(O)R27, -OCH2C(O)NHR27, -OC(O)R27, -OC(O)OR27, -OC(O)NHNH-R5, or -OC(O)NR27R28, where R27 and R28 are each independentlyH, C1 -C20 alkyl, cycloalkyl, alkenyl, aryl, arylalkyl, or alkylaryl, and where R27 and R28 can each optionally contain halogen atoms; R23 and R24, the same or different from each other, are C1-C20 alkyl, cycloalkyl, alkenyl, aryl, arylalkyl, or alkylaryl. Methods of using such formulations for the treatment of cancer, to effect weight loss, to treat microbially-based infections, to inhibit neuropeptide-Y and/or fatty acid synthase, and to stimulate CPT-1.

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