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73881-19-3

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73881-19-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73881-19-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,8,8 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73881-19:
(7*7)+(6*3)+(5*8)+(4*8)+(3*1)+(2*1)+(1*9)=153
153 % 10 = 3
So 73881-19-3 is a valid CAS Registry Number.
InChI:InChI=1/C25H40O4/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-18-23-19-17-20-24(28-21(2)26)25(23)29-22(3)27/h17,19-20H,4-16,18H2,1-3H3

73881-19-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-acetyloxy-3-pentadecylphenyl) acetate

1.2 Other means of identification

Product number -
Other names 3-n-Pentadecylcatechol diacetate

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:73881-19-3 SDS

73881-19-3Downstream Products

73881-19-3Relevant articles and documents

Study of two isoforms of lipoxygenase by kinetic assays, docking and molecular dynamics of a specialised metabolite isolated from the aerial portion of Lithrea caustica (Anacardiaceae) and its synthetic analogs

Mascayano-Collado, Carolina,Mu?oz-Ramírez, Alejandra,Torrent-Farías, Claudia,Urzúa-Moll, Alejandro

, (2020/03/27)

Our investigation focused on the characterization and study of epicuticular leaf extracts (dichloromethane extract) and certain derivatives of Lithrea caustica (Molina) Hook and Arn. (Anacardiaceae) as inhibitors of 15 soybean and 5 human lipoxygenases (1

Synthesis and antiallergenic properties of 3-n-pentadecyl- and 3-n-heptadecylcatechol esters

Elsohly,Benigni,Torres,Watson

, p. 792 - 795 (2007/10/02)

A synthetic procedure is described for the preparation of 3-n-pentadecyl- and 3-n-heptadecylcatechols and their acetate and alaninate esters. The Wittig reagent prepared from 2,3-dimethoxybenzyltriphenylphosphonium bromide (III) was coupled with 1-tetrade

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