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13533-18-1

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13533-18-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13533-18-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,3 and 3 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13533-18:
(7*1)+(6*3)+(5*5)+(4*3)+(3*3)+(2*1)+(1*8)=81
81 % 10 = 1
So 13533-18-1 is a valid CAS Registry Number.
InChI:InChI=1/C21H38O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-23-21(22)4-2/h4,11-12H,2-3,5-10,13-20H2,1H3/b12-11-

13533-18-1SDS

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 octadec-9-enyl prop-2-enoate

1.2 Other means of identification

Product number -
Other names Oleyl acrylate

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:13533-18-1 SDS

13533-18-1Downstream Products

13533-18-1Relevant articles and documents

Efficient organic solvent and oil sorbent co-polyesters: Poly-9-octadecenylacrylate/methacrylate with 1-hexene

Dutta, Priyanka,Gogoi, Bedanta,Dass, Narendra Nath,Sen Sarma, Neelotpal

, p. 457 - 464 (2013)

In this work, highly absorbent cross linked co-polymer gels of cis-9-octadecen-1-ol with acrylic/methacrylic acid and 1-hexene in different molar ratios were synthesized by thermal polymerization techniques and studied. The polymers were characterized by

A three-step-one-pot chemo-enzymatic synthesis of epoxyalkanolacylates

Klaas, M. Ruesch,Warwel

, p. 251 - 260 (2007/10/03)

Using the ability of Novozym 435 to catalyze both the perhydrolysis and the interesterification of esters, unsaturated primary alcohols are converted with an ester and hydrogen peroxide to give esters of epoxidized alcohols directly in a convenient three-step-one-pot synthesis with yields of 66-89%.

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