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17511-60-3

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  • Tricyclodecenyl propionate Manufacturer Herbal Propionate Factory CAS 17511-60-3

    Cas No: 17511-60-3

  • USD $ 1.2-5.0 / Kiloliter

  • 5 Kiloliter

  • 3000 Metric Ton/Month

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17511-60-3 Usage

Safety Profile

A skin irritant. When heated todecomposition it emits acrid smoke and irritating vapors.

Check Digit Verification of cas no

The CAS Registry Mumber 17511-60-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,1 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 17511-60:
(7*1)+(6*7)+(5*5)+(4*1)+(3*1)+(2*6)+(1*0)=93
93 % 10 = 3
So 17511-60-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H18O2/c1-2-13(14)15-12-7-8-6-11(12)10-5-3-4-9(8)10/h3-4,8-12H,2,5-7H2,1H3

17511-60-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Herbal Propionate

1.2 Other means of identification

Product number -
Other names Dicyclopentenyl propionate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Fragrances
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:17511-60-3 SDS

17511-60-3Downstream Products

17511-60-3Relevant articles and documents

Process for making tricyclodecenyl esters

-

Page/Page column 6; 7, (2008/12/04)

A practical, economical process for making tricyclodecenyl esters is disclosed. After reacting a lower carboxylic acid and a dicyclopentadiene in the presence of triflic acid to form the ester, the reaction mixture is distilled in the presence of a base to isolate a fragrance-quality tricyclodecenyl ester. Adding enough base to neutralize the triflic acid enables a distillation-only purification, facilitates starting material recovery, and avoids drawbacks of a basic workup.

Synthesis of esters by addition of carboxylic acids to cage cycloolefins

Mamedov

, p. 165 - 168 (2007/10/03)

The thermal addition of monocarboxylic acids to cage bi-, tri-, tetra-, and pentacyclic hydrocarbons was carried out, and a highly efficient wasteless method of preparing esters of the corresponding alcohols was developed. The reaction has no need for Lewis acids as special catalysts since the initial acids themselves function as both catalyst and reagent. Orientation of the formyloxy and acyloxy groups in cycloolefin hydrocarbons was found, and the degree of regio- and stereoselectivity of the reaction was determined. A number of new esters of polycyclic alcohols were prepared. Some of them are of interest for perfumes.

Photooxidation and 13C N.M.R. Spectroscopic Investigation of 5,6-Dihydrodicyclopentadiene Derivatives

Fanghaenel, E.,Keita, Y.,Radeglia, R.,Schmidt, W.

, p. 837 - 846 (2007/10/02)

The sensitized photooxidation of endo-5,6-dihydrodicyclopentadiene (2) by singulet oxygen gives via the corresponding hydroperoxide (10) exo-1-hydroxy-5,6-dihydrodicyclopentadiene (7a).Starting from exo-5,6-dihydrodicyclopentadiene (6) exo-5,6-dihydrodicyclopentadien-1-one (12) is formed.The 13C n.m.r. spectroscopical data of these compounds and of other hydroxy, alkoxy and acyloxy dihydrodicyclopentadiene derivatives are discussed in relation on their structure.

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