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CAS

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562847-17-0

11-Hexadecynoic acid, 10-(acetyloxy)-16-(phenylmethoxy)-, methyl ester, (10R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

562847-17-0

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  • 11-Hexadecynoic acid, 10-(acetyloxy)-16-(phenylmethoxy)-, methyl ester, (10R)-

    Cas No: 562847-17-0

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562847-17-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 562847-17-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,2,8,4 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 562847-17:
(8*5)+(7*6)+(6*2)+(5*8)+(4*4)+(3*7)+(2*1)+(1*7)=180
180 % 10 = 0
So 562847-17-0 is a valid CAS Registry Number.

562847-17-0SDS

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 methyl 10-acetoxy-16-benzyloxy-11-hexadecynoate

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:562847-17-0 SDS

562847-17-0Downstream Products

562847-17-0Relevant articles and documents

Synthesis of (R)- and (S)-10,16-dihydroxyhexadecanoic acid: Cutin stereochemistry and fungal activation

Ahmed, Aqeel,Crawford, Terry,Gould, Stephanie,Ha,Hollrah, Monica,Noor-E-Ain, Farhana,Dickman, Martin B.,Dussault, Patrick H.

, p. 47 - 52 (2007/10/03)

The first asymmetric syntheses of the cutin monomers (R)- and (S)-10,16-dihydroxyhexadecanoic acid (10,16-DHPA) and confirmation of (S)(+)-absolute configuration for 10, 16-DHPA derived from tomato are reported. The individual DHPA stereoisomers display differences in their ability to activate the fungal pathogen Colletotrichum trifolii.

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