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2-HYDROXY-5-METHOXY-3-TRIDECYL-[1,4]BENZOQUINONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 19833-82-0 Structure
  • Basic information

    1. Product Name: 2-HYDROXY-5-METHOXY-3-TRIDECYL-[1,4]BENZOQUINONE
    2. Synonyms: 2-HYDROXY-5-METHOXY-3-TRIDECYL-[1,4]BENZOQUINONE;Rapanone, derivative of
    3. CAS NO:19833-82-0
    4. Molecular Formula: C20H32O4
    5. Molecular Weight: 336.47
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 19833-82-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 464.7°C at 760 mmHg
    3. Flash Point: 154.6°C
    4. Appearance: /
    5. Density: 1.04g/cm3
    6. Vapor Pressure: 1.37E-10mmHg at 25°C
    7. Refractive Index: 1.502
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-HYDROXY-5-METHOXY-3-TRIDECYL-[1,4]BENZOQUINONE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-HYDROXY-5-METHOXY-3-TRIDECYL-[1,4]BENZOQUINONE(19833-82-0)
    12. EPA Substance Registry System: 2-HYDROXY-5-METHOXY-3-TRIDECYL-[1,4]BENZOQUINONE(19833-82-0)
  • 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: 19833-82-0(Hazardous Substances Data)

19833-82-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19833-82-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,3 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19833-82:
(7*1)+(6*9)+(5*8)+(4*3)+(3*3)+(2*8)+(1*2)=140
140 % 10 = 0
So 19833-82-0 is a valid CAS Registry Number.
InChI:InChI=1/C20H32O4/c1-3-4-5-6-7-8-9-10-11-12-13-14-16-19(22)17(21)15-18(24-2)20(16)23/h15,22H,3-14H2,1-2H3

19833-82-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Hydroxy-5-methoxy-3-tridecyl-1,4-benzoquinone

1.2 Other means of identification

Product number -
Other names Methyl 2-hydroxy-5-methoxy-3-nitrobenzenecarboxylate

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:19833-82-0 SDS

19833-82-0Relevant articles and documents

First synthesis of N-(3-carboxylpropyl)-5-amino-2-hydroxy-3-tridecyl-1,4- benzoquinone, an unusual quinone isolated from Embelia ribes

McErlean, Christopher S. P.,Moody, Christopher J.

, p. 10298 - 10301 (2007)

(Chemical Equation Presented) The first synthesis of the unusual nitrogen-containing 3-alkyl-1,4-benzoquinone, N-(3-carboxylpropyl)-5-amino-2- hydroxy-3-tridecyl-1,4-benzoquinone, isolated from Embelia ribes, is reported. The key steps are a microwave-ass

Design, synthesis and α-glucosidase inhibition study of novel embelin derivatives

Chen, Wenhua,Chen, Xiaole,Gao, Min,Hong, Weiqian David,Jian, Rongchao,Li, Yuling,Sheng, Zhaojun,Tang, Xiaowen,Wu, Panpan,Zhang, Kun,Zhao, Denggao,Zheng, Xi

, p. 565 - 573 (2020/02/15)

Embelin is a naturally occurring para-benzoquinone isolated from Embelia ribes (Burm. f.) of the Myrsinaceae family. It was first discovered to have potent inhibitory activity (IC50 = 4.2 μM) against α-glucosidase in this study. Then, four seri

Novel series of benzoquinones with high potency against 5-lipoxygenase in human polymorphonuclear leukocytes

Filosa, Rosanna,Peduto, Antonella,Schaible, Anja M.,Krauth, Verena,Weinigel, Christina,Barz, Dagmar,Petronzi, Carmen,Bruno, Ferdinando,Roviezzo, Fiorentina,Spaziano, Giuseppe,D'Agostino, Bruno,De Rosa, Mario,Werz, Oliver

, p. 132 - 139 (2015/04/14)

5-Lipoxygenase (5-LO) is a potential target for pharmacological intervention with various inflammatory and allergic diseases. Starting from the natural dual 5-LO/microsomal prostaglandin E2 synthase (mPGES)-1 inhibitor embelin (2,5-dihydroxy-3-

MULTIFUNCTIONAL RADICAL QUENCHERS

-

, (2014/05/07)

The invention provides a compound of formula (I): [insert formula (I)] wherein X, Y, and R1-R4 have any of the values defined in the specification, and salts thereof, as well as compositions comprising the compounds or salts. The compounds are useful for treating diseases associated with impaired mitochondrial function in an animal.

Synthesis and biological activities of N-(3-Carboxylpropyl)-5-amino-2- hydroxy-3-tridecyl-1,4-benzoquinone and analogues

Madathil, Manikandadas M.,Khdour, Omar M.,Jaruvangsanti, Jennifer,Hecht, Sidney M.

, p. 2209 - 2215 (2013/02/25)

The synthesis of benzoquinone natural product 2 and three analogues is described. The synthesized compounds were tested for their ability to protect Friedreich's ataxia (FRDA) lymphocytes from induced oxidative stress. One of the analogues (3) conferred c

Total synthesis of maesanin and analogues

Poigny, Stephane,Guyot, Michele,Samadi, Mohammad

, p. 14791 - 14802 (2007/10/03)

An efficient total synthesis of maesanin and related quinones is reported, through direct alkylation of 1,2,4,5-tetramethoxybenzene with alkylbromides, followed by oxidation with ceric ammonium nitrate (CAN) which provokes formation of the quinone and dep

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