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1,2-Benzenediol, 3-(8Z)-8-heptadecenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54954-20-0

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54954-20-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54954-20-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,9,5 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 54954-20:
(7*5)+(6*4)+(5*9)+(4*5)+(3*4)+(2*2)+(1*0)=140
140 % 10 = 0
So 54954-20-0 is a valid CAS Registry Number.

54954-20-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[(Z)-heptadec-8-enyl]benzene-1,2-diol

1.2 Other means of identification

Product number -
Other names Heptadecenylcatechol

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:54954-20-0 SDS

54954-20-0Relevant academic research and scientific papers

The synthesis and identification of alkenyl and alkadienyl catechols of burmese lac

Sargent, Melvyn V.,Wangchareontrakul, Sirichai,Jefferson, Alan

, p. 431 - 439 (2007/10/02)

The presence of (Z)-(4), (E)-3-(heptadec-8'-enyl)-(5), (Z)-4-(heptadec-8'- enyl)-benzene-1,2-diol (47), (Z,Z)-3-(heptadeca-8',11'-dienyl)-(1), and (Z,Z)-4-(heptadeca-8',11'-dienyl)-benzene-1,2-diol (3) in Burmese lac, the sap of Melanorrhoea usitata, has

Synthesis of Urushiol Derivatives by the Fries Rearrangement

Jefferson, Alan,Wangchareontrakul, Sirichai

, p. 605 - 614 (2007/10/02)

The photo- and thermal-induced Fries rearrangement reactions of some unsaturated aliphatic esters of benzene-1,2-diol (catechol) have been studied.Photorearrangement and thermal rearrangement favoured products correspond to ortho and para migration respectively, but the thermal rearrangement may be acompanied by indanones, chromanones and other products which were formed through subsequent side reactions of the double bond.Photoinduced Fries rearrangement of 2-hydroxyphenyl oleate followed by reduction of the carbonyl group gave monosubstituted catechol derivatives with an unsaturated C18 side chain in either the 3- or 4-position.These alkenylcatechol derivatives are related in structure to chemical components isolated from oriental lacquer trees, such as urushiol from Rhus verniciflua or thitsiol from Melanorrhoea usitata

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