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22474-42-6

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22474-42-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22474-42-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,4,7 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 22474-42:
(7*2)+(6*2)+(5*4)+(4*7)+(3*4)+(2*4)+(1*2)=96
96 % 10 = 6
So 22474-42-6 is a valid CAS Registry Number.

22474-42-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl gyrophorate

1.2 Other means of identification

Product number -
Other names Gyrophorsaeure-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:22474-42-6 SDS

22474-42-6Downstream Products

22474-42-6Relevant articles and documents

NMR Assignments of Depsides and Tridepsides of the Lichen Family Umbilicariaceae

Narui, Takao,Sawada, Keiko,Takatsuki, Satoshi,Okuyama, Toru,Culberson, Chicita F.,et al.

, p. 815 - 822 (1998)

NMR spectral analysis provides important information for the identification of secondary products of chemotaxonomic significance in the lichen genera Umbilicaria and Lasallia (Umbilicariaceae). Two depsides (evernic and lecanoric acids) and eight tridepsides (crustinic, gyrophoric, hiascic, lasallic, 4-O-methylgyrophoric, ovoic and umbilicaric acids and tenuiorin) were isolated from various unrelated lichens. Seven of the ten compounds are important taxonomic characters in the family Umbilicariaceae. 1H and 13C NMR spectral signals were assigned for the compounds and for methyl esters of lecanoric, evernic and gyrophoric acids. Using these NMR data and mass spectrometry, chemical structures were elucidated for two new compounds, papulosic acid (2,6-dihydroxy-3-carboxy-4-methylphenyl orsellinate) from the umbilicariaceous Lasallia papulosa and deliseic acid (lecanoryl 3-acetoxy-4,6-dihydroxy-2-methylbenzoate) from the parmeliaceous Cetrariella delisei.

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