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80373-18-8

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80373-18-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80373-18-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,3,7 and 3 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 80373-18:
(7*8)+(6*0)+(5*3)+(4*7)+(3*3)+(2*1)+(1*8)=118
118 % 10 = 8
So 80373-18-8 is a valid CAS Registry Number.

80373-18-8SDS

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 3-(4-hydroxyphenyl)propyl acetate

1.2 Other means of identification

Product number -
Other names 3-(4'-hydroxyphenyl)-1-propyl acetate

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:80373-18-8 SDS

80373-18-8Downstream Products

80373-18-8Relevant articles and documents

Synthesis and structure/antioxidant activity relationship of novel catecholic antioxidant structural analogues to hydroxytyrosol and its lipophilic esters

Bernini, Roberta,Crisante, Fernanda,Barontini, Maurizio,Tofani, Daniela,Balducci, Valentina,Gambacorta, Augusto

experimental part, p. 7408 - 7416 (2012/10/08)

A large panel of novel catecholic antioxidants and their fatty acid or methyl carbonate esters has been synthesized in satisfactory to good yields through a 2-iodoxybenzoic acid (IBX)-mediated aromatic hydroxylation as the key step. The new catechols are

Microwave-accelerated selective acylation of (hydroxyalkyl)phenols using acid chlorides

Miyazawa, Toshifumi,Yamamoto, Masato,Maeda, Yuki

experimental part, p. 1092 - 1099 (2009/09/06)

Highly selective acylation of the alcoholic hydroxy group can be achieved with (hydroxyalkyl)phenols carrying both alcoholic and phenolic hydroxyls by the use of the most common acylating agents, acid chlorides, under microwave irradiation. Copyright Tayl

Selective acylation of a sterically hindered hydroxyl group of unsymmetrical diols containing a primary hydroxyl group such as 1,5-hexanediol in the presence of silica gel with acetyl chloride

Ogawa, Haruo,Ide, Yuko,Honda, Ryoichi,Chihara, Teiji

, p. 355 - 358 (2007/10/03)

The selective acetylation of sterically hindered hydroxyl groups of 1,5-hexanediol preadsorbed on silica gel was reported. The relation between the adsorption of the diol on SiO2 and its reactivity for selective acetylation was studied. Results demonstrated that unsymmetrical diols get adsorbed on the surface of SiO2 preferentially via a primary OH group, leaving the non-adsorbed OH group available for reaction.

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