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2-Acetyl-3-methylnaphthalene-1,6,8-triol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23520-25-4

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23520-25-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23520-25-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,5,2 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 23520-25:
(7*2)+(6*3)+(5*5)+(4*2)+(3*0)+(2*2)+(1*5)=74
74 % 10 = 4
So 23520-25-4 is a valid CAS Registry Number.

23520-25-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Hydroxymusizin

1.2 Other means of identification

Product number -
Other names 1-(1,6,8-Trihydroxy-3-methyl-[2]naphthyl)-aethanon

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:23520-25-4 SDS

23520-25-4Downstream Products

23520-25-4Relevant academic research and scientific papers

Xanthouroleuconaphin: A yellowish pigment from the aphid Uroleucon nigrotuberculatum and its total synthesis

Nishimura, Taichi,Horikawa, Mitsuyo,Yamada, Kouji,Sogabe, Ayaka,Nishii, Takeshi,Kaku, Hiroto,Inai, Makoto,Tanaka, Masami,Takahashi, Shigeru,Tsunoda, Tetsuto

, p. 1808 - 1814 (2013)

A novel yellowish pigment, xanthouroleuconaphin, was isolated from the aphid Uroleucon nigrotuberculatum. Its structure was established by detailed analyses of 1D and 2D NMR spectra and EI-HRMS. Furthermore, the total synthesis of (±)-xanthouroleuconaphin was accomplished via oxidative phenolic coupling of 6-hydroxymusizin, which was prepared by the Fries rearrangement using BF3·2AcOH complex.

Asymmetric synthesis of natural cis-dihydroarenediols using tetrahydroxynaphthalene reductase and its biosynthetic implications

Saha, Nirmal,Müller, Michael,Husain, Syed Masood

, p. 2204 - 2208 (2019/03/29)

Asymmetric reduction of hydroxynaphthoquinones to secondary metabolites, (3S,4R)-3,4,8- A nd (2S,4R)-2,4,8-trihydroxy-1-tetralone, a putative biosynthetic diketo intermediate and a probable natural analogue, (3S,4R)-7-acetyl-3,4,8-trihydroxy-6-methyl-3,4-

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