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85003-85-6

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85003-85-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85003-85-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,0,0 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 85003-85:
(7*8)+(6*5)+(5*0)+(4*0)+(3*3)+(2*8)+(1*5)=116
116 % 10 = 6
So 85003-85-6 is a valid CAS Registry Number.

85003-85-6SDS

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 3,8-dihydroxy-6-methyl-9-oxo-9H-xanthene-1-carboxylic acid methyl ester

1.2 Other means of identification

Product number -
Other names 3,8-Dihydroxy-6-methyl-9-oxo-xanthen-1-carbonsaeure-methylester

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:85003-85-6 SDS

85003-85-6Downstream Products

85003-85-6Relevant articles and documents

Bioactive sulfur-containing sulochrin dimers and other metabolites from an alternaria sp. isolate from a Hawaiian soil sample

Cai, Shengxin,King, Jarrod B.,Du, Lin,Powell, Douglas R.,Cichewicz, Robert H.

, p. 2280 - 2287 (2014)

Polluxochrin (1) and dioschrin (2), two new dimers of sulochrin linked by thioether bonds, were purified from an Alternaria sp. isolate obtained from a Hawaiian soil sample. The structures of the two metabolites were established by NMR, mass spectrometry data, and X-ray analysis. Metabolite 1 was determined to be susceptible to intramolecular cyclization under aqueous conditions, resulting in the generation of 2 as well as another dimeric compound, castochrin (3). An additional nine new metabolites were also obtained, including four new pyrenochaetic acid derivatives (8-11), one new asterric acid analogue (13), and four new secalonic acid analogues (14-17). Bioassay analysis of these compounds revealed 1-3 displayed antimicrobial and weak cytotoxic activities.

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