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6,8-dihydroxy-1-methylisochroman-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77053-29-3

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77053-29-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77053-29-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,0,5 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 77053-29:
(7*7)+(6*7)+(5*0)+(4*5)+(3*3)+(2*2)+(1*9)=133
133 % 10 = 3
So 77053-29-3 is a valid CAS Registry Number.

77053-29-3SDS

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 6,8-dihydroxy-1-methylisochroman-3-one

1.2 Other means of identification

Product number -
Other names -

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:77053-29-3 SDS

77053-29-3Downstream Products

77053-29-3Relevant academic research and scientific papers

Mechanistic studies on the biomimetic reduction of tetrahydroxynaphthalene, a key intermediate in melanin biosynthesis

Ichinose,Ebizuka,Sankawa

, p. 192 - 196 (2001)

1,3,6,8-Tetrahydroxynaphthalene (T4HN) is an aromatic polyketide, serving as a general precursor of fungal melanin. Melanin biosynthesis involves two consecutive deoxygenations of T4HN, consisting of the reduction of a phenolic carbon followed by dehydrat

DEOXYGENATION IN THE BIOSYNTHESIS OF POLYKETIDES: MECHANISM OF BIOMIMETIC REDUCTION OF TETRAHYDROXYNAPHTHALENE

Ichinose, Koji,Ebizuka, Yutaka,Sankawa, Ushio

, p. 2873 - 2875 (2007/10/02)

A biomimetic synthesis of scytalone, a simple derivative of tetralone, was reinvestigeted using NMR spectroscopy.Scytalone was formed from 1,3,6,8-tetrahydroxynaphthalene (1,3,6,8-THN) by sodium borohydride reduction only in the presence of sodium methoxi

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