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146-04-3

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146-04-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146-04-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,4 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 146-04:
(5*1)+(4*4)+(3*6)+(2*0)+(1*4)=43
43 % 10 = 3
So 146-04-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H8O5/c12-4-9(14)7-5-16-11(15)10-6(7)2-1-3-8(10)13/h1-3,5,12-13H,4H2

146-04-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-hydroxy-4-(2-hydroxyacetyl)isochromen-1-one

1.2 Other means of identification

Product number -
Other names 4-glycoloyl-8-hydroxy-1H-isochromen-1-one

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:146-04-3 SDS

146-04-3Upstream product

146-04-3Downstream Products

146-04-3Related news

Biosynthesis of Oosponol (cas 146-04-3) and oospoglycol elucidated by 1 3 C NMR09/28/2019

The biosynthesis of the antibiotic metabolities oosponol and oospoglycol by the fungus Gloeophyllum abietinum has been analysed using 1 3 C-labelled acetate, malonate, serine and formate as precursors and 1 3 C NMR as the analytical method. The polyketide pathway could b...detailed

146-04-3Relevant articles and documents

Secondary fungal metabolites and their biological activity, VIII: Partial synthesis of oosponol, an antifungal isocoumarin

Kovacs, Tiber,Sonnenbichler, Johann

, p. 211 - 212 (1997)

The partial synthesis of oosponol (4), which shows significant antibiotic activity, has been accomplished by enzyme catalyzed reactions including regioselective acetylation of (-)-oospoglycol (1) followed by an oxidation step and hydrolysis by a lipase. VCH Verlagsgesellschaft mbH, 1997.

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